| Year |
Citation |
Score |
| 2013 |
Meyers AI, Lawson J, Amos RA, Walker DG, Spohn RF. Studies on the total synthesis of streptogramin anti-biotics: Griseoviridin and madumycin (A-2315A) Pure and Applied Chemistry. 54: 2537-2544. DOI: 10.1002/Chin.198323372 |
0.311 |
|
| 2010 |
ES-SAYED M, GRATKOWSKI C, KRASS N, MEYERS AI, DE MEIJERE A. ChemInform Abstract: Cyclopropyl Building Blocks for Organic Synthesis. Part 14. Optically Active Oxazolidinones as Michael Donors for the Short and Efficient Synthesis of β-Amino Acids Containing a Cyclopropane Ring. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199323265 |
0.345 |
|
| 2005 |
Meyers AI. Chiral oxazolines and their legacy in asymmetric carbon-carbon bond-forming reactions. The Journal of Organic Chemistry. 70: 6137-51. PMID 16050670 DOI: 10.1021/Jo050470H |
0.456 |
|
| 2004 |
Meyers AI, Nelson TD, Moorlag H, Rawson DJ, Meier A. Chiral oxazoline route to enantiomerically pure biphenyls: Magnesio and copper mediated asymmetric hetero- and homo-coupling reactions Tetrahedron. 60: 4459-4473. DOI: 10.1016/J.Tet.2004.01.095 |
0.486 |
|
| 2003 |
Tschantz MA, Burgess LE, Meyers AI. S-(−)-5-Heptyl-2-Pyrrolidinone. Chiral Bicyclic Lactams as Templates for Pyrrolidines and Pyrrolidinones Organic Syntheses. 221-221. DOI: 10.1002/0471264180.Os073.22 |
0.452 |
|
| 2003 |
Tschantz MA, Burgess LE, Meyers AI. 4‐Ketoundecanoic Acid Organic Syntheses. 215-215. DOI: 10.1002/0471264180.Os073.21 |
0.389 |
|
| 2003 |
Meyers AI, Flanagan ME. 2,2′‐Dimethoxy‐6‐Formylbiphenyl Organic Syntheses. 107-107. DOI: 10.1002/0471264180.Os071.14 |
0.424 |
|
| 2003 |
Meyers AI, Berney D. Asymmetric Synthesis of 4,4‐Dialkylcyclohexenones from Chiral Bicyclic Lactams: (R)‐4‐Ethyl‐4‐allyl‐2‐cyclohexen‐1‐one Organic Syntheses. 55-55. DOI: 10.1002/0471264180.Os069.07 |
0.459 |
|
| 2003 |
Brinkmeyer RS, Collington EW, Meyers AI. Aldehydes from 4,4‐Dimethyl‐2‐Oxazoline and Grignard Reagents: o‐Anisaldehyde Organic Syntheses. 42-42. DOI: 10.1002/0471264180.Os054.08 |
0.319 |
|
| 2003 |
Politzer IR, Meyers AI. Aldehydes from 2-Benzyl-4,4,6-Trimethyl-5,6-Dihydro-1,3(4H)-Oxazine: 1-Phenylcyclopentanecarboxaldehyde Organic Syntheses. 24-24. DOI: 10.1002/0471264180.Os051.07 |
0.312 |
|
| 2002 |
Basil LF, Nakano H, Frutos R, Kopach M, Meyers AI. Asymmetric tandem additions to chiral 2,3-dihydronaphthyloxazolines: Synthesis of the triptoquinone/triptinin a ring system Synthesis. 2064-2074. DOI: 10.1055/S-2002-34373 |
0.496 |
|
| 2002 |
Basil LF, Meyers AI, Hassner A. Asymmetric conjugate additions to chiral α,β-unsaturated oxazolines with sulfonyl carbanions Tetrahedron. 58: 207-213. DOI: 10.1016/S0040-4020(01)01151-6 |
0.429 |
|
| 2002 |
Meyers AI, Dickman DA, Bailey TR. Asymmetric Synthesis of 2‐Alkylpyrrolidines and Piperidines. Synthesis of (+)‐Metazocine. Cheminform. 17. DOI: 10.1002/Chin.198616142 |
0.515 |
|
| 2002 |
Meyers AI, Poindexter GS, Brich Z. Asymmetric Synthesis Of (+)‐ Or (‐)‐2‐Methyloctanal Via The Metalloenamines Of Chiral Alkoxy Amines Cheminform. 9. DOI: 10.1002/Chin.197830148 |
0.553 |
|
| 2001 |
Hillier MC, Price AT, Meyers AI. Studies on the total synthesis of disorazole C1. An advanced macrocycle intermediate. The Journal of Organic Chemistry. 66: 6037-45. PMID 11529729 DOI: 10.1021/Jo010249E |
0.422 |
|
| 2001 |
Hughes RC, Dvorak CA, Meyers AI. An asymmetric approach to spirocylic systems: a formal synthesis of zizaene. The Journal of Organic Chemistry. 66: 5545-51. PMID 11485481 DOI: 10.1021/Jo010439P |
0.509 |
|
| 2001 |
Meyers AI, Downing SV, Weiser MJ. Asymmetric synthesis of 2-alkyl-perhydroazepines from [5,3,0]-bicyclic lactams. The Journal of Organic Chemistry. 66: 1413-9. PMID 11312974 DOI: 10.1021/Jo001548R |
0.44 |
|
| 2001 |
Waterson AG, Kruger AW, Meyers AI. Studies directed toward the synthesis of viridenomycin. Route 2: A second generation approach Tetrahedron Letters. 42: 4305-4308. DOI: 10.1016/S0040-4039(01)00701-8 |
0.423 |
|
| 2001 |
Kruger AW, Meyers AI. Studies directed toward the synthesis of viridenomycin. Route 1: Assembly of three advanced intermediates Tetrahedron Letters. 42: 4301-4304. DOI: 10.1016/S0040-4039(01)00700-6 |
0.441 |
|
| 2001 |
Groaning MD, Brengel GP, Meyers AI. Allyldimethyltritylsilane: Construction of enantiomerically pure cyclobutano[c]fused pyrrolidines Tetrahedron. 57: 2635-2642. DOI: 10.1016/S0040-4020(01)00083-7 |
0.817 |
|
| 2000 |
Waterson AG, Meyers AI. Bicyclic lactams as chiral homoenolate equivalents: synthesis of (-)-penienone. The Journal of Organic Chemistry. 65: 7240-3. PMID 11031061 DOI: 10.1021/Jo000860Y |
0.546 |
|
| 2000 |
Degnan AP, Meyers AI. Enantioselective synthesis of rigid 2-aminotetralins. Utility of silicon as an oxygen and nitrogen surrogate in the tandem addition reaction. The Journal of Organic Chemistry. 65: 3503-12. PMID 10843638 DOI: 10.1021/jo0001131 |
0.369 |
|
| 2000 |
Dvorak CA, Schmitz WD, Poon DJ, Pryde DC, Lawson JP, Amos RA, Meyers AI. The Synthesis of Streptogramin Antibiotics: (-)-Griseoviridin and Its C-8 Epimer Financial support has been provided by the National Institutes of Health (NIH). We thank the NIH for financial support of this study and Drs. Russell Linderman, Donald Walker, Ronald Spohn, and Enrico Marcantoni for their assistance in various stages of this effort. Angewandte Chemie (International Ed. in English). 39: 1664-1666. PMID 10820470 DOI: 10.1002/(Sici)1521-3773(20000502)39:9<1664::Aid-Anie1664>3.0.Co;2-# |
0.681 |
|
| 2000 |
Kolotuchin SV, Meyers AI. Asymmetric and nonasymmetric addition of RLi and RMgX to 3-methoxynaphthalen-2-yl oxazolines and imines. An approach to substituted 2-tetralones The Journal of Organic Chemistry. 65: 3018-26. PMID 10814192 |
0.414 |
|
| 2000 |
Groaning MD, Meyers AI. Concise synthesis of indolizidines: Total synthesis of (-)-coniceine Chemical Communications. 1027-1028. DOI: 10.1039/B002621M |
0.82 |
|
| 2000 |
Waterson AG, Meyers AI. Bicyclic lactamz as chiral homoenolate equivalents: Synthesis of (-)-penienone Journal of Organic Chemistry. 65: 7240-7243. DOI: 10.1021/jo000860y |
0.45 |
|
| 2000 |
Watson DJ, Meyers AI. Asymmetric route to the hydroindolone core of the Amaryllidaceae alkaloids employing chiral bicyclic lactams Tetrahedron Letters. 41: 1519-1522. DOI: 10.1016/S0040-4039(99)02328-X |
0.521 |
|
| 2000 |
Watson DJ, Devine PN, Meyers AI. Palladium and nickel catalyzed thio-claisen rearrangements of chiral bicyclic thiolactams (via N,S-ketene acetals) Tetrahedron Letters. 41: 1363-1367. DOI: 10.1016/S0040-4039(99)02294-7 |
0.382 |
|
| 2000 |
Watson DJ, Lawrence CM, Meyers AI. Remote chiral induction in the thio-Claisen rearrangement of bicyclic thiolactams Tetrahedron Letters. 41: 815-818. DOI: 10.1016/S0040-4039(99)02199-1 |
0.415 |
|
| 2000 |
Oda K, Meyers AI. An efficient route to chiral, non-racemic 3-alkyl-3-arylpyrrolidines. Improved stereoselectivity in alkylation of bicyclic lactams and the effect of leaving groups Tetrahedron Letters. 41: 8193-8197. DOI: 10.1016/S0040-4039(00)01471-4 |
0.536 |
|
| 2000 |
Mechelke MF, Meyers AI. An efficient, enantioselective synthesis of branched polyhydroxylated pyrrolidines Tetrahedron Letters. 41: 9377-9381. DOI: 10.1016/S0040-4039(00)01452-0 |
0.508 |
|
| 2000 |
Mechelke MF, Meyers AI. An efficient, asymmetric synthesis of (+)-euphococcinine Tetrahedron Letters. 41: 4339-4342. DOI: 10.1016/S0040-4039(00)00665-1 |
0.54 |
|
| 2000 |
Hillier MC, Park DH, Price AT, Ng R, Meyers AI. The synthesis of the monomeric moiety of disorazole C1 Tetrahedron Letters. 41: 2821-2824. DOI: 10.1016/S0040-4039(00)00271-9 |
0.403 |
|
| 2000 |
Groaning MD, Meyers AI. Chiral non-racemic bicyclic lactams. Auxiliary-based asymmetric reactions Tetrahedron. 56: 9843-9873. DOI: 10.1016/S0040-4020(00)00926-1 |
0.809 |
|
| 1999 |
Lemieux RM, Devine PN, Mechelke MF, Meyers AI. An Asymmetric Route to Novel Chiral Cyclohexenones with Spiro-Connected Cyclopentenes. Further Utility of Chiral Bicyclic Thiolactams and the [3,3] Thio-Claisen Products. The Journal of Organic Chemistry. 64: 3585-3591. PMID 11674485 DOI: 10.1021/Jo982426Q |
0.472 |
|
| 1999 |
Downing SV, Aguilar E, Meyers AI. Total Synthesis of Bistratamide D. The Journal of Organic Chemistry. 64: 826-831. PMID 11674153 DOI: 10.1021/Jo981664I |
0.37 |
|
| 1999 |
Kamata K, Sato H, Takagi E, Agata I, Meyers AI. Synthesis of optically active 2-chloromethyl-2-oxazolines by the ortho- ester condensation method using triethyl orthochloroacetate Heterocycles. 51: 373-378. DOI: 10.3987/Com-98-8407 |
0.711 |
|
| 1999 |
Kolotuchin SV, Meyers AI. Synthesis of 8,8'-disubstituted 1,1'-binaphthyls stable to atropisomerization: 2,2'-dimethyl-1,1'-binaphthalene-8,8'-diol and 2,2'- dimethyl-8,8'-bis(4-tert-butyloxazolyl)-1,1'-binaphthyl Journal of Organic Chemistry. 64: 7921-7928. DOI: 10.1021/Jo990968H |
0.366 |
|
| 1999 |
Degnan AP, Meyers AI. Total syntheses of (-)-herbertenediol, (-)-mastigophorene A, and (-)- mastigophorene B. Combined utility of chiral bicyclic lactams and chiral aryl oxazolines Journal of the American Chemical Society. 121: 2762-2769. DOI: 10.1021/ja984182x |
0.361 |
|
| 1999 |
Dwyer MP, Lamar JE, Meyers AI. Synthesis of enantiomerically pure cis-2,4-disubstituted piperidines: Extension of chiral homoenolate alkylations toward the preparation of nitrogen heterocycles Tetrahedron Letters. 40: 8965-8968. DOI: 10.1016/S0040-4039(99)01784-0 |
0.495 |
|
| 1999 |
Groaning MD, Meyers AI. Remote steric effects in the Sakurai reaction Tetrahedron Letters. 40: 8071-8074. DOI: 10.1016/S0040-4039(99)01703-7 |
0.797 |
|
| 1999 |
Dwyer MP, Price DA, Lamar JE, Meyers AI. An asymmetric oxazoline ketenimine rearrangement. Construction of chiral α-quaternary carbon ketones Tetrahedron Letters. 40: 4765-4768. DOI: 10.1016/S0040-4039(99)00729-7 |
0.456 |
|
| 1999 |
Groaning MD, Meyers AI. An asymmetric synthesis of the key precursor to (-)-indolizomycin Tetrahedron Letters. 40: 4639-4642. DOI: 10.1016/S0040-4039(99)00728-5 |
0.826 |
|
| 1999 |
Reeder MR, Meyers AI. Asymmetric routes to the trisporic acids via chiral bicyclic lactams Tetrahedron Letters. 40: 3115-3118. DOI: 10.1016/S0040-4039(99)00454-2 |
0.5 |
|
| 1999 |
Meyers AI, Andres CJ, Resek JE, Woodall CC, McLaughlin MA, Lee PH, Price DA. Asymmetric routes to azasugars from chiral bicyclic lactams. Synthesis of 1,4-dideoxy-1,4-imino-d-lyxitol; L-Deoxymannojirimycin; rhammo-1- Deoxynojirimycin and 1-deoxy-6-epicastanospermine Tetrahedron. 55: 8931-8952. DOI: 10.1016/S0040-4020(99)00454-8 |
0.533 |
|
| 1999 |
Arrington MP, Meyers AI. Asymmetric synthesis of the core cyclopentane of viridenomycin Chemical Communications. 1371-1372. |
0.358 |
|
| 1998 |
Meyers AI, Price A. The Unique Behavior of a Chiral Binaphthyl Oxazoline in the Presence of Cu(I) and Its Role as a Chiral Catalyst. The Journal of Organic Chemistry. 63: 412-413. PMID 11672018 DOI: 10.1021/Jo971761W |
0.335 |
|
| 1998 |
Meyers AI, Price DA. Asymmetric syntheses of 1-deoxy-6-epicastanospermine and rhamno-1-deoxynojirimycin. Chirality. 10: 88-90. PMID 9470208 DOI: 10.1002/Chir.14 |
0.556 |
|
| 1998 |
Groaning MD, Brengel GP, Meyers AI. Allyldimethyltritylsilane. Synthesis of Cyclopentanols, Oxetanes, and Tetrahydrofurans by Reaction with Electron Deficient Olefins Journal of Organic Chemistry. 63: 5517-5522. DOI: 10.1021/Jo9805652 |
0.813 |
|
| 1998 |
Schwarz JB, Meyers AI. Asymmetric synthesis of a constituent of iris essential oil by homoenolate alkylation of a chiral bicyclic lactam Journal of Organic Chemistry. 63: 1732-1735. DOI: 10.1021/Jo9719214 |
0.408 |
|
| 1998 |
Schwarz JB, Meyers AI. Tandem α-Cyano Enamine/Enolate Alkylations on Bicyclic Lactams: Asymmetric Carbocycle and Heterocycle Synthesis Journal of Organic Chemistry. 63: 1619-1629. DOI: 10.1021/Jo971920B |
0.536 |
|
| 1998 |
Kamata K, Agata I, Meyers AI. An Efficient and Versatile Method for the Synthesis of Optically Active 2-Oxazolines: An Acid-catalyzed Condensation of Ortho Esters with Amino Alcohols The Journal of Organic Chemistry. 63: 3113-3116. DOI: 10.1021/Jo971161X |
0.723 |
|
| 1998 |
Meyers AI, Seefeld MA, Lefker BA, Blake JF, Williard PG. Stereoselective alkylations in rigid systems. Effect of remote substituents on π-facial additions to lactam enolates. Stereoelectronic and steric effects Journal of the American Chemical Society. 120: 7429-7438. DOI: 10.1021/Ja980614S |
0.458 |
|
| 1998 |
Lemieux RM, Meyers AI. Asymmetric synthesis of (-)-trichodiene. Generation of vicinal stereogenic quaternary centers via the thio-Claisen rearrangement Journal of the American Chemical Society. 120: 5453-5457. DOI: 10.1021/ja9804159 |
0.413 |
|
| 1998 |
James B, Meyers AI. Diastereoselective conjugate additions of ethoxyvinyllithium to aromatic and α,β-unsaturated oxazolines Tetrahedron Letters. 39: 5301-5304. DOI: 10.1016/S0040-4039(98)01072-7 |
0.417 |
|
| 1998 |
Hughes R, Meyers AI. A route to chiral, non-racemic macroheterocycles Tetrahedron. 54: 9895-9902. DOI: 10.1016/S0040-4020(98)00560-2 |
0.474 |
|
| 1998 |
Meyers AI, Willemsen JJ. An oxazoline based approach to (S)-gossypol Tetrahedron. 54: 10493-10511. DOI: 10.1016/S0040-4020(98)00501-8 |
0.347 |
|
| 1998 |
Meyers AI. Chiral oxazolines - Their legacy as key players in the renaissance of asymmetric synthesis Journal of Heterocyclic Chemistry. 35: 991-1002. DOI: 10.1002/Jhet.5570350501 |
0.525 |
|
| 1997 |
Meyers AI, Nguyen T, Stoianova D, Sreerama N, Woody RW, Koslowski A, Fleischhauer J. Synthesis and chiroptical properties of a novel C2-symmetric binaphthyl phosphortriamide ("chiral HMPA"). Chirality. 9: 431-4. PMID 9329175 DOI: 10.1002/(Sici)1520-636X(1997)9:5/6<431::Aid-Chir6>3.0.Co;2-8 |
0.425 |
|
| 1997 |
Meyers AI, Price DA, Andres CJ. Asymmetric synthesis of L-deoxymannojirimycin Synlett. 533-534. DOI: 10.1055/S-1997-6112 |
0.358 |
|
| 1997 |
Meyers AI, Willemsen JJ. The synthesis of (S)-(+)-gossypol via an asymmetric Ullmann coupling Chemical Communications. 1573-1574. DOI: 10.1039/A703043F |
0.474 |
|
| 1997 |
Meyers AI, Brengel GP. Chiral bicyclic lactams: Useful precursors and templates for asymmetric syntheses Chemical Communications. 1-8. DOI: 10.1039/A604443C |
0.486 |
|
| 1997 |
Meyers AI, Stoianova D. Short asymmetric synthesis of (+)-α-curcumene and (+)-xanthorrhizol Journal of Organic Chemistry. 62: 5219-5221. DOI: 10.1021/Jo970429H |
0.416 |
|
| 1997 |
Meyers AI, Seefeld MA, Lefker BA, Blake JF. Origin of stereochemistry in simple pyrrolidinone enolate alkylations Journal of the American Chemical Society. 119: 4565-4566. DOI: 10.1021/Ja970173X |
0.455 |
|
| 1997 |
Shimano M, Meyers AI. α-Ethoxyvinyllithium·HMPA. Further studies on its unusual basic properties Tetrahedron Letters. 38: 5415-5418. DOI: 10.1016/S0040-4039(97)01203-3 |
0.354 |
|
| 1997 |
Meyers AI, Akahane A, Struzka V, Warmus JS, Gonzalez M, Milot G. A reinvestigation of the reported synthesis of the spironzyl isoquinoline alkaloid, iso-ochotensine Tetrahedron Letters. 38: 4195-4198. DOI: 10.1016/S0040-4039(97)00869-1 |
0.427 |
|
| 1997 |
Schwarz JB, Devine PN, Meyers AI. Chiral bicyclic lactams as homoenolate equivalents: An asymmetric route to 5-substituted cyclohexenones Tetrahedron. 53: 8795-8806. DOI: 10.1016/S0040-4020(97)90391-4 |
0.512 |
|
| 1996 |
Munchhof MJ, Meyers AI. A Novel Asymmetric Route to the 1,3-Disubstituted Tetrahydroisoquinoline, (-)-Argemonine. The Journal of Organic Chemistry. 61: 4607-4610. PMID 11667387 DOI: 10.1021/Jo960110H |
0.491 |
|
| 1996 |
Meyers AI, Andres CJ, Resek JE, McLaughlin MA, Woodall CC, Lee PH. A Rapid and Efficient Approach to Chiral, Nonracemic Aza Sugars from Nonsugars. A Formal Synthesis of 1,4-Dideoxy-1,4-imino-D-lyxitol. The Journal of Organic Chemistry. 61: 2586-2587. PMID 11667079 DOI: 10.1021/Jo960129K |
0.432 |
|
| 1996 |
Matulenko MA, Meyers AI. Total Synthesis of (-)-Tetrahydropalmatine via Chiral Formamidine Carbanions: Unexpected Behavior with Certain Ortho-Substituted Electrophiles. The Journal of Organic Chemistry. 61: 573-580. PMID 11666977 DOI: 10.1021/jo951611q |
0.414 |
|
| 1996 |
Meyers AI, Hutchings R. Asymmetric dialkylation of chiral 2-benzazepine formamidines Heterocycles. 42: 475-478. DOI: 10.3987/Com-95-S58 |
0.454 |
|
| 1996 |
Meyers AI, Seefeld MA, Lefker BA. Chiral bicyclic lactams. A new study on facial alkylation Journal of Organic Chemistry. 61: 5712-5713. DOI: 10.1021/Jo960952G |
0.424 |
|
| 1996 |
Shimano M, Meyers AI. Diastereoselective 1,6-additions of lithium amides to naphthyloxazolines. A route to novel δ-amino acid derivatives Journal of Organic Chemistry. 61: 5714-5715. DOI: 10.1021/Jo960874X |
0.404 |
|
| 1996 |
Brengel GP, Meyers AI. Tritylallyldimethylsilane - TiCl4 annulations to electron deficient olefins. Diastereomerically pure 3-substituted and 3,4-disubstituted cyclopentanols Journal of Organic Chemistry. 61: 3230-3231. DOI: 10.1021/Jo9601021 |
0.328 |
|
| 1996 |
Fray AH, Meyers AI. Single and double diastereoselection in azomethine ylide cycloaddition reactions with unsaturated chiral bicyclic lactams Journal of Organic Chemistry. 61: 3362-3374. DOI: 10.1021/Jo9600870 |
0.402 |
|
| 1996 |
Hutchings RH, Meyers AI. An oxazoline-mediated synthesis of the pyrrolophenanthridine alkaloids and some novel derivatives Journal of Organic Chemistry. 61: 1004-1013. DOI: 10.1021/Jo951474X |
0.446 |
|
| 1996 |
Kopach ME, Fray AH, Meyers AI. An asymmetric route to the conanine BCDE ring system. A formal total synthesis of (+)-conessine Journal of the American Chemical Society. 118: 9876-9883. DOI: 10.1021/Ja961903O |
0.52 |
|
| 1996 |
Tavares F, Lawson JP, Meyers AI. Total synthesis of streptogramin antibiotics. (-)-Madumycin II Journal of the American Chemical Society. 118: 3303-3304. DOI: 10.1021/Ja954312R |
0.346 |
|
| 1996 |
Pryde DC, Henry SS, Meyers AI. Synthesis of 2-tetralones via a novel 1,2-carbonyl transposition of 1-tetralones Tetrahedron Letters. 37: 3243-3246. DOI: 10.1016/0040-4039(96)00522-9 |
0.518 |
|
| 1996 |
Meyers AI, Novachek KA. Pd-mediated cross-coupling of aryl, alkenyl, and alkynyl stannanes with chiral 2-bromo oxazolines Tetrahedron Letters. 37: 1747-1748. DOI: 10.1016/0040-4039(96)00165-7 |
0.374 |
|
| 1996 |
Novachek KA, Meyers AI. A convenient procedure for the reduction of S-(+)-silyl serine methyl ester to chiral serinol derivatives Tetrahedron Letters. 37: 1743-1746. DOI: 10.1016/0040-4039(96)00164-5 |
0.472 |
|
| 1996 |
Meyers AI, Willemsen JJ. An asymmetric synthesis of (+)-apogossypol hexamethyl ether Tetrahedron Letters. 37: 791-792. DOI: 10.1016/0040-4039(95)02296-1 |
0.509 |
|
| 1996 |
Meyers AI, Bienz S, Kwon H, Wallace RH. The Asymmetric Synthesis of Fused Cyclopentenone Ring Systems: A formal asymmetric total synthesis of (−)‐isocomene Helvetica Chimica Acta. 79: 1026-1046. DOI: 10.1002/Hlca.19960790412 |
0.517 |
|
| 1996 |
Meyers AI, Bienz S, Kwon HB, Wallace RH. 90. The asymmetric synthesis of fused cyclopentenone ring systems: A formal asymmetric total synthesis of (-)-isocomene Helvetica Chimica Acta. 79: 1026-1046. |
0.368 |
|
| 1995 |
Resek JE, Meyers AI. Intramolecular Photochemical [2+2] Cycloadditions of Enantiomerically Pure 4,4-Disubstituted Cyclohexenones: An Approach to the Total Asymmetric Synthesis of Lintenone Synlett. 1995: 145-146. DOI: 10.1055/S-1995-4900 |
0.5 |
|
| 1995 |
Sandham DA, Meyers AI. Chiral bicyclic lactams - An asymmetric synthesis of the framework of the Lycopodium alkaloid magellanine containing all six adjacent stereogenic centres Journal of the Chemical Society, Chemical Communications. 2511-2512. DOI: 10.1039/C39950002511 |
0.45 |
|
| 1995 |
Es-Sayed M, Devine P, Burgess LE, De Meijere A, Meyers AI. An asymmetric synthesis of novel aminocyclopropyl carboxylic acids (ACC) Journal of the Chemical Society, Chemical Communications. 141-142. DOI: 10.1039/C39950000141 |
0.459 |
|
| 1995 |
Shimano M, Meyers AI. Asymmetric diastereoselective conjugate additions of lithium amides to chiral naphthyloxazolines leading to novel β-amino acids Journal of Organic Chemistry. 60: 7445-7455. DOI: 10.1021/Jo00128A016 |
0.431 |
|
| 1995 |
Munchhof MJ, Meyers AI. A novel route to chiral, nonracemic 1-alkyl- and 1-aryl-substituted tetrahydroisoquinolines. Synthesis of (-)-salsolidine and (+)-cryptostyline II The Journal of Organic Chemistry. 60: 7086-7087. DOI: 10.1021/Jo00127A006 |
0.522 |
|
| 1995 |
Munchhof MJ, Meyers AI. An asymmetric route to chiral, nonracemic 2-substituted piperidines. Synthesis of (-)-pipecoline, (+)-coniine, and (-)-coniceine The Journal of Organic Chemistry. 60: 7084-7085. DOI: 10.1021/Jo00127A005 |
0.558 |
|
| 1995 |
Schwarz JB, Meyers AI. Synthesis of vicinal stereogenic tertiary and quaternary centers using chiral bicyclic lactams and diastereoselective protonation. Asymmetric synthesis of (+)-Laurene Journal of Organic Chemistry. 60: 6511-6514. DOI: 10.1021/Jo00125A042 |
0.546 |
|
| 1995 |
Meyers AI, Tschantz MA, Brengel GP. Asymmetric Lewis acid-catalyzed addition of a ketene dithioacetal to a chiral bicyclic lactam. Formation of cyclobutanopyrrolidinones. A new class of GABA derivatives Journal of Organic Chemistry. 60: 4359-4362. DOI: 10.1021/Jo00119A012 |
0.399 |
|
| 1995 |
Andres CJ, Lee PH, Nguyen TH, Meyers AI. Asymmetric conjugate additions to chiral bicyclic lactams. A stereoselective general synthesis of chiral 3-aminopyrrolidines The Journal of Organic Chemistry. 60: 3189-3193. DOI: 10.1021/Jo00115A040 |
0.531 |
|
| 1995 |
Hulme AN, Henry SS, Meyers AI. Asymmetric synthesis of the key intermediates leading to (-)-aphanorphine and (-)-eptazocine Journal of Organic Chemistry. 60: 1265-1270. DOI: 10.1021/Jo00110A033 |
0.517 |
|
| 1995 |
Munchhof MJ, Meyers AI. A novel asymmetric route to chiral, nonracemic cis-2,6-disubstituted piperidines. Synthesis of (+)-pinidinone and (+)-monomorine Journal of the American Chemical Society. 117: 5399-5400. DOI: 10.1021/Ja00124A039 |
0.479 |
|
| 1995 |
Resek JE, Meyers AI. Unsaturation of ketones, nitriles and lactams with methyl phenylsulfinate Tetrahedron Letters. 36: 7051-7054. DOI: 10.1016/0040-4039(95)01461-P |
0.426 |
|
| 1995 |
Meyers AI, Santiago B. C2 symmetric amines. III. An asymmetric synthesis of (S,S)-1,3-dialkyl lsoindolines by sequential formamidine alkylation Tetrahedron Letters. 36: 5877-5880. DOI: 10.1016/0040-4039(95)01182-H |
0.435 |
|
| 1995 |
Meyers AI, Nguyen TH. C2 symmetric amines. II. Asymmetric synthesis of C2 (3S,3'S)-and (3R, 3′R) dimethyl 4H-dinaphth [2, 1-c:1′, 2′-e] azepines Tetrahedron Letters. 36: 5873-5876. DOI: 10.1016/0040-4039(95)01181-G |
0.378 |
|
| 1995 |
Meyers AI, McKennon MJ. C2 symmetric amines. I. The asymmetric Ullmann synthesis of a new C2-symmetric binaphthyl Tetrahedron Letters. 36: 5869-5872. DOI: 10.1016/0040-4039(95)01180-P |
0.424 |
|
| 1995 |
Andres CJ, Meyers AI. Asymmetric conjugate additions to chiral bicyclic lactams. A stereoselective, concise synthesis of chiral 2-alkyl-3,4-aziridinopyrrolidines Tetrahedron Letters. 36: 3491-3494. DOI: 10.1016/0040-4039(95)00573-U |
0.511 |
|
| 1995 |
Andres CJ, Spetseris N, Norton JR, Meyers AI. Non-metallocatalyzed epoxidation of chiral unsaturated lactams by tertiary amine N-oxides Tetrahedron Letters. 36: 1613-1616. DOI: 10.1016/0040-4039(95)00114-R |
0.375 |
|
| 1994 |
Meyers AI, Nguyen TH. An asymmetric synthesis of S-(-)-noranicanine Heterocycles. 39: 513-518. DOI: 10.3987/Com-94-S(B)17 |
0.441 |
|
| 1994 |
Nelson TD, Meyers AI. The asymmetric Ullmann reaction. 2. The synthesis of enantiomerically pure C2-symmetric binaphthyls Journal of Organic Chemistry. 59: 2655-2658. DOI: 10.1021/Jo00088A066 |
0.458 |
|
| 1994 |
Nelson TD, Meyers AI. A rapid total synthesis of an ellagitannin Journal of Organic Chemistry. 59: 2577-2580. DOI: 10.1021/Jo00088A046 |
0.435 |
|
| 1994 |
Hulme AN, Meyers AI. Asymmetric synthesis of 1,1-disubstituted tetralins and dihydronaphthalenes by diastereoselective addition of lithiosilanes to chiral naphthalenes Journal of Organic Chemistry. 59: 952-953. DOI: 10.1021/Jo00084A007 |
0.544 |
|
| 1994 |
Shimano M, Meyers AI. Asymmetric Michael-Type Additions of Lithium Amides to Aromatic Systems Leading to Novel .beta.-Amino Acids Journal of the American Chemical Society. 116: 6437-6438. DOI: 10.1021/Ja00093A055 |
0.323 |
|
| 1994 |
Devine PN, Meyers AI. Thio-Claisen rearrangements. An asymmetric synthesis of 4,4-disubstituted cyclohexenones with vicinal quaternary and tertiary stereocenters Journal of the American Chemical Society. 116: 2633-2634. DOI: 10.1021/Ja00085A059 |
0.553 |
|
| 1994 |
Westrum LJ, Meyers AI. A Synthesis of Enantiomerically Pure 3- and 3,3-Disubstituted Pyrrolidines Tetrahedron Letters. 35: 973-976. DOI: 10.1016/S0040-4039(00)79942-4 |
0.553 |
|
| 1994 |
Scialdone MA, Meyers AI. A stereoselective concise synthesis of C2- and meso-aminodiols from (R)-phenylglycinol Tetrahedron Letters. 35: 7533-7536. DOI: 10.1016/S0040-4039(00)78336-5 |
0.381 |
|
| 1994 |
Aguilar E, Meyers AI. Total synthesis of (-)-bistatramide C Tetrahedron Letters. 35: 2477-2480. DOI: 10.1016/S0040-4039(00)77148-6 |
0.442 |
|
| 1994 |
Aguilar E, Meyers AI. Reinvestigation of a modified Hantzsch thiazole synthesis Tetrahedron Letters. 35: 2473-2476. DOI: 10.1016/S0040-4039(00)77147-4 |
0.462 |
|
| 1994 |
Alexakis A, Frutos JC, Mangeney P, Meyers AI, Moorlag H. Determination of enantiomeric purity of hydroxy biaryls using 1H and 31P-NMR on their diazaphospholidine derivatives Tetrahedron Letters. 35: 5125-5128. DOI: 10.1016/S0040-4039(00)77044-4 |
0.406 |
|
| 1994 |
Nelson TD, Meyers AI. The asymmetric Ullmann reaction III. Application of a first-order asymmetric transformation to the synthesis of C2-symmetric chiral, non-racemic biaryls Tetrahedron Letters. 35: 3259-3262. DOI: 10.1016/S0040-4039(00)76879-1 |
0.426 |
|
| 1994 |
Elworthy TR, Meyers AI. The configurational stability of chiral lithio α-amino carbanions. The effect of Li-O vs. Li-N complexation Tetrahedron. 50: 6089-6096. DOI: 10.1016/S0040-4020(01)90460-0 |
0.354 |
|
| 1994 |
Gant TG, Meyers AI. The chemistry of 2-oxazolines (1985-present) Tetrahedron. 50: 2297-2360. DOI: 10.1016/S0040-4020(01)86953-2 |
0.359 |
|
| 1994 |
Tavares F, Meyers AI. Further studies on oxazoline and thiazoline oxidations. A reliable route to chiral oxazoles and thiazoles Tetrahedron Letters. 35: 6803-6806. DOI: 10.1016/0040-4039(94)85009-7 |
0.412 |
|
| 1994 |
Shimano M, Meyers AI. Enolate free α-alkoxyvinyllithium reagents: Improved preparation and reaction with N,N-dialkylcarboxamides Tetrahedron Letters. 35: 7727-7730. DOI: 10.1016/0040-4039(94)80103-7 |
0.347 |
|
| 1993 |
Meyers AI, Schmidt W, McKennon MJ. Asymmetric addition to chiral aromatic and unsaturated oxazolines using a novel chiral auxillary Synthesis. 250-262. DOI: 10.1055/S-1993-25842 |
0.455 |
|
| 1993 |
Newhouse BJ, Meyers AI, Sirisoma NS, Braun MP, Johnson CR. Preparation of α-Halo-α,β-Unsaturated Bicyclic Lactams and Their Use in Palladium-Catalyzed Cross Coupling Reactions Synlett. 1993: 573-574. DOI: 10.1055/S-1993-22533 |
0.354 |
|
| 1993 |
Snyder L, Meyers AI. Synthesis of enantiomerically pure hydrinden-2-ones and benz[e]inden-2-ones via asymmetric alkylations of chiral bicyclic lactams Journal of Organic Chemistry. 58: 7507-7515. DOI: 10.1021/Jo00078A032 |
0.361 |
|
| 1993 |
Meyers AI, Milot G. Regioselectivity in forming dipole-stabilized anions. Sites of metalation of indolines, tetrahydroquinolines, and benzazepines activated by N-formimidoyl or N-boc groups Journal of Organic Chemistry. 58: 6538-6540. DOI: 10.1021/Jo00076A003 |
0.312 |
|
| 1993 |
McKennon MJ, Meyers AI, Drauz K, Schwarm M. A convenient reduction of amino acids and their derivatives Journal of Organic Chemistry. 58: 3568-3571. DOI: 10.1021/Jo00065A020 |
0.419 |
|
| 1993 |
Meyers AI, Snyder L. The synthesis of aracemic 4-substituted pyrrolidinones and 3-substituted pyrrolidines. An asymmetric synthesis of (-)-Rolipram Journal of Organic Chemistry. 58: 36-42. DOI: 10.1021/Jo00053A012 |
0.529 |
|
| 1993 |
Meyers AI, Milot G. .alpha.-Alkylation and stereochemistry of cis- and trans-decahydroquinolines mediated by the formamidine and Boc activating groups. Synthesis of pumiliotoxin C Journal of the American Chemical Society. 115: 6652-6660. DOI: 10.1021/Ja00068A023 |
0.426 |
|
| 1993 |
Nelson TD, Meyers AI. The synthesis of a useful chiral biaryl catalyst. An oxazoline-mediated Ullmann reaction Tetrahedron Letters. 34: 3061-3062. DOI: 10.1016/S0040-4039(00)93379-3 |
0.44 |
|
| 1993 |
Gant TG, Meyers AI. Oxazoline-mediated synthesis of the Gossypium sesquiterpene lacinilene C-7 methyl ether and a structurally Related HIV-1 Reverse Transcriptase Inhibitor Tetrahedron Letters. 34: 3707-3710. DOI: 10.1016/S0040-4039(00)79206-9 |
0.372 |
|
| 1993 |
Meyers AI, Shimano M. A facile cleavage of oxazolines to carbinols Tetrahedron Letters. 34: 4893-4896. DOI: 10.1016/S0040-4039(00)74039-1 |
0.374 |
|
| 1993 |
Santiago B, Meyers AI. Formamidine anions in synthesis. The one-carbon homologation of aldehydes and ketones to nitriles Tetrahedron Letters. 34: 5839-5842. DOI: 10.1016/S0040-4039(00)73793-2 |
0.42 |
|
| 1993 |
Meyers AI, Hutchings RH. A total synthesis of the pyrrolophenthridone alkaloid oxoassoanine Tetrahedron Letters. 34: 6185-6188. DOI: 10.1016/S0040-4039(00)73705-1 |
0.461 |
|
| 1993 |
Moorlag H, Meyers AI. An asymmetric synthesis of a C2 symmetric tetrasubstituted biaryl: 2,2′-Dihydroxy-6,6′-dimethyl-1,1′-biphenyl, a stable chiral system Tetrahedron Letters. 34: 6993-6996. DOI: 10.1016/S0040-4039(00)61579-4 |
0.518 |
|
| 1993 |
Moorlag H, Meyers AI. Oxazoline-mediated biaryl coupling reactions. Stereocontrolled synthesis of 2,2′,6,6′-tetrasubstituted biphenyls Tetrahedron Letters. 34: 6989-6992. DOI: 10.1016/S0040-4039(00)61578-2 |
0.445 |
|
| 1993 |
Es-Sayed M, Gratkowski C, Krass N, Meyers AI, de Meijere A. Optically active oxazolidinones as Michael donors for the short and efficient synthesis of β-amino acids containing a cyclopropane ring Tetrahedron Letters. 34: 289-292. DOI: 10.1016/S0040-4039(00)60569-5 |
0.462 |
|
| 1993 |
Meyers AI, Hutchings RH. The asymmetric synthesis of 1-alkyl-2,3,4,5-tetrahydro-benzazepines and benzo[β]-1-azabicyclo[5,3,1]decanes Tetrahedron. 49: 1807-1820. DOI: 10.1016/S0040-4020(01)80537-8 |
0.554 |
|
| 1992 |
Es-Sayed M, Gratkowski C, Krass N, Meyers AI, Meijere Ad. Optically Active Oxazolidinones as Michael Donors: Synthesis of Novel Enantiopure α,β-Diamino Acids and 2-Substituted 1-Aminocyclopropane Carboxylic Acids1 Synlett. 1992: 962-964. DOI: 10.1055/S-1992-21545 |
0.406 |
|
| 1992 |
Rawson D, Meyers AI. The asymmetric reduction of prochiral ketones using (S)-2,2′- dihydroxy-4,5,6,4′,5′,6′-hexamethoxybiphenyl Journal of the Chemical Society, Chemical Communications. 494-496. DOI: 10.1039/C39920000494 |
0.454 |
|
| 1992 |
Romo D, Meyers AI. An asymmetric route to enantiomerically pure 1,2,3-trisubstituted cyclopropanes Journal of Organic Chemistry. 57: 6265-6270. DOI: 10.1021/Jo00049A038 |
0.731 |
|
| 1992 |
Meyers AI, Elworthy TR. Chiral formamidines. The total asymmetric synthesis of (-)-8-azaestrone and related (-)-8-aza-12-oxo-17-desoxoestrone Journal of Organic Chemistry. 57: 4732-4740. DOI: 10.1021/Jo00043A036 |
0.53 |
|
| 1992 |
Meyers AI, Gant TG. A synthesis of various substituted naphthalenones by additions to naphthyloxazolines Journal of Organic Chemistry. 57: 4225-4231. DOI: 10.1021/Jo00041A030 |
0.465 |
|
| 1992 |
Castonguay LA, Guiles JW, Rappé AK, Meyers AI. Asymmetric alkylations on chiral formamidines. Molecular mechanics studies relating to the facial selectivity of the lithiated intermediates Journal of Organic Chemistry. 57: 3819-3821. DOI: 10.1021/Jo00040A019 |
0.353 |
|
| 1992 |
Meyers AI, Snyder L. Asymmetric conjugate additions to chiral bicyclie lactams. Synthesis of aracemic trans-2,3-disubstituted pyrrolidines Journal of Organic Chemistry. 57: 3814-3819. DOI: 10.1021/Jo00040A018 |
0.448 |
|
| 1992 |
Sielecki TM, Meyers AI. Formamidines in synthesis. An efficient one-pot synthesis of 7-substituted indolines via intramolecular cyclization of (2-phenethyl)formamidines. An asymmetric route to benzopyrrocoline alkaloids Journal of Organic Chemistry. 57: 3673-3676. DOI: 10.1021/Jo00039A029 |
0.456 |
|
| 1992 |
Burgess LE, Meyers AI. A simple asymmetric synthesis of 2-substituted pyrrolidines and 5-substituted pyrrolidinones Journal of Organic Chemistry. 57: 1656-1662. DOI: 10.1021/Jo00032A012 |
0.517 |
|
| 1992 |
Meyers AI, Sielecki TM, Crans DC, Marshman RW, Nguyen TH. (-)-Cryptaustoline: Its synthesis, revision of absolute stereochemistry, and mechanism of inversion of stereochemistry Journal of the American Chemical Society. 114: 8490-8496. DOI: 10.1021/Ja00048A020 |
0.427 |
|
| 1992 |
Gant TG, Meyers AI. Regiospecific synthesis of polysubstituted naphthalenes via oxazoline-mediated nucleophilic aromatic substitutions and additions Journal of the American Chemical Society. 114: 1010-1015. DOI: 10.1021/Ja00029A032 |
0.537 |
|
| 1992 |
Fray AH, Meyers AI. Diastereoselective azomethine ylide cycloadditions to unsaturated, chiral bicyclic lactams Tetrahedron Letters. 33: 3575-3578. DOI: 10.1016/S0040-4039(00)92506-1 |
0.491 |
|
| 1992 |
Meyers AI, Robichaud AJ, McKennon MJ. The synthesis of chiral α,β-unsaturated and aryl oxazolines from ketones and arols via their triflates and pd-catalyzed CO and amino alcohol coupling Tetrahedron Letters. 33: 1181-1184. DOI: 10.1016/S0040-4039(00)91890-2 |
0.426 |
|
| 1992 |
Meyers AI, Shawe TT, Gottlieb L. Stereoselective nucleophilic addition to conformationally constrained piperidines. An efficient route to 2-axial-6-equatorial disubstituted piperidines Tetrahedron Letters. 33: 867-870. DOI: 10.1016/S0040-4039(00)91562-4 |
0.488 |
|
| 1992 |
Meyers AI, Meier A, Rawson DJ. A highly stereoselective synthesis of axially chiral biaryls. Application to the synthesis of a potential chiral catalysts Tetrahedron Letters. 33: 853-856. DOI: 10.1016/S0040-4039(00)91558-2 |
0.497 |
|
| 1992 |
Meyers AI. Recent progress using chiral formamidines in asymmetric syntheses Tetrahedron. 48: 2589-2612. DOI: 10.1016/S0040-4020(01)88523-9 |
0.46 |
|
| 1991 |
Busacca CA, Meyers AI. Asymmetric Diels-Alder reactions. A route to chiral carbocycles via bicyclic lactams Journal of the Chemical Society, Perkin Transactions 1. 2299-2316. DOI: 10.1039/P19910002299 |
0.478 |
|
| 1991 |
Meyers AI, Shipman M. Asymmetric Michael additions to .alpha.,.beta.-unsaturated oxazolines. An efficient preparation of chiral .beta.,.beta.-disubstituted propionaldehydes Journal of Organic Chemistry. 56: 7098-7102. DOI: 10.1021/Jo00025A027 |
0.418 |
|
| 1991 |
Guiles JW, Meyers AI. Asymmetric synthesis of benzoquinolizidines: A formal synthesis of (-)-emetine Journal of Organic Chemistry. 56: 6873-6878. DOI: 10.1021/Jo00024A032 |
0.51 |
|
| 1991 |
Dupré B, Meyers AI. An improved synthesis of ethyl N-(methoxycarbonyl)-2,5-dihydro-1H-pyrrole-3-carboxylate Journal of Organic Chemistry. 56: 3197-3198. DOI: 10.1021/Jo00009A053 |
0.387 |
|
| 1991 |
Meyers AI, Highsmith TK, Buonora PT. Asymmetric synthesis of yohimban alkaloids. Total synthesis of (-)-pseudo- and (-)-alloyohimban Journal of Organic Chemistry. 56: 2960-2964. DOI: 10.1021/Jo00009A007 |
0.522 |
|
| 1991 |
Shawe TT, Meyers AI. Stereochemistry of alkylation of .alpha.-lithio piperidines: differing effects of formamidine and urethane activating groups Journal of Organic Chemistry. 56: 2751-2755. DOI: 10.1021/Jo00008A033 |
0.401 |
|
| 1991 |
Robichaud AJ, Meyers AI. Asymmetric additions to chiral naphthyloxazolines. An entry into tetracyclic terpene ring systems related to aphidicolin, scopadulcic acid, and kauranes Journal of Organic Chemistry. 56: 2607-2609. DOI: 10.1021/Jo00008A003 |
0.41 |
|
| 1991 |
Meyers AI, Burgess LE. A simple asymmetric synthesis of 2-substituted pyrrolidines from 3-acylpropionic acids Journal of Organic Chemistry. 56: 2294-2296. DOI: 10.1021/Jo00007A011 |
0.448 |
|
| 1991 |
Rawson DJ, Meyers AI. Asymmetric tandem additions to chiral naphthyloxazolines. A new and potent chiral auxiliary resulting in a major improvement in convenience and efficiency Journal of Organic Chemistry. 56: 2292-2294. DOI: 10.1021/Jo00007A010 |
0.46 |
|
| 1991 |
Beard RL, Meyers AI. Asymmetric synthesis of the corynantheine alkaloids via an intramolecular Blaise reaction. (-)-Corynantheidol and (-)-dihydrocoryanantheol Journal of Organic Chemistry. 56: 2091-2096. DOI: 10.1021/jo00006a024 |
0.37 |
|
| 1991 |
Leonard WR, Romine JL, Meyers AI. A rapid and efficient synthesis of chiral 2-hydro 2-oxazolines Journal of Organic Chemistry. 56: 1961-1963. DOI: 10.1021/Jo00005A059 |
0.439 |
|
| 1991 |
Burgess LE, Meyers AI. Asymmetric synthesis of .gamma.,.gamma.-dialkyl-.gamma.-aminobutyric acid analogs and 2,2-disubstituted pyrrolidines. Control of stereochemistry in aminal ring opening by varying the extent of allylic 1,3 strain Journal of the American Chemical Society. 113: 9858-9859. DOI: 10.1021/Ja00026A026 |
0.367 |
|
| 1991 |
Meyers AI, M.sielecki T. Total synthesis of the dibenzopyrrocoline alkaloid (S)-(+)-cryptaustoline. Revision of absolute configuration due to an unusual inversion in stereochemistry Journal of the American Chemical Society. 113: 2789-2790. DOI: 10.1021/Ja00007A084 |
0.347 |
|
| 1991 |
Meyers AI, Leonard WR, Romine JL. Highly diastereoselective addition to a novel chiral oxazinone. Further approaches to chiral quaternary carbon compounds Tetrahedron Letters. 32: 597-600. DOI: 10.1016/S0040-4039(00)74836-2 |
0.454 |
|
| 1991 |
Rawson DJ, Meyers AI. Highly reactive organolithiums (from "Freeman's Reagent") and their additions to naphthalene oxazolines Tetrahedron Letters. 32: 2095-2098. DOI: 10.1016/S0040-4039(00)71245-7 |
0.374 |
|
| 1991 |
Romo D, Meyers AI. Chiral non-racemic bicyclic lactams. Vehicles for the construction of natural and unnatural products containing quaternary carbon centers Tetrahedron. 47: 9503-9569. DOI: 10.1016/S0040-4020(01)91024-5 |
0.688 |
|
| 1991 |
Meyers AI, Warmus JS, Gonzalez MA, Guiles J, Akahane A. Chiral formamidines. The mechanism of mono- and di-alkylation leading to chiral, non-racemic tetrahydroisoquinolines Tetrahedron Letters. 32: 5509-5512. DOI: 10.1016/0040-4039(91)80070-M |
0.443 |
|
| 1991 |
Meyers AI, Guiles J, Warmus JS, Gonzalez MA. Chiral lithio formamidines. Are they configurationally stable? Tetrahedron Letters. 32: 5505-5508. DOI: 10.1016/0040-4039(91)80069-I |
0.368 |
|
| 1991 |
Meyers AI, Gonzalez MA, Struzka V, Akahane A, Guiles J, Warmus JS. Chiral formamidines. Asymmetric synthesis of 1,1-disubstituted tetrahydroisoquinolines Tetrahedron Letters. 32: 5501-5504. DOI: 10.1016/0040-4039(91)80068-H |
0.506 |
|
| 1991 |
Burgess LE, Meyers AI. Asymmetric synthesis of γ,γ-dialkyl-γ-aminobutyric acid analogues and 2,2-disubstituted pyrrolidines. Control of stereochemistry in aminal ring opening by varying the extent of allylic 1,3-strain Journal of the American Chemical Society. 113: 9858-9859. |
0.304 |
|
| 1990 |
Gottlieb L, Meyers AI. An asymmetric synthesis of aporphine and related alkaloids via chiral formamidines. (+)-Glaucine, (+)-homoglaucine, and (-)-8,9-didemethoxythalisopavine Journal of Organic Chemistry. 55: 5659-5662. DOI: 10.1021/Jo00308A029 |
0.506 |
|
| 1990 |
Wünsch T, Meyers AI. Asymmetric synthesis of 4,4-disubstituted 1-naphthalenones. Diastereoselectivity as a function of metal alkoxides Journal of Organic Chemistry. 55: 4233-4235. DOI: 10.1021/Jo00301A002 |
0.33 |
|
| 1990 |
Meyers AI, Du B, Gonzalez MA. The synthesis of 1,1′-spiroalkane or fused annulated 1,2,3,4-tetrahydroisoquinolines using a highly reactive formamidine for metalation-alkylation Journal of Organic Chemistry. 55: 4218-4220. DOI: 10.1021/Jo00300A052 |
0.371 |
|
| 1990 |
Meyers AI, Bienz S. Asymmetric total synthesis of (+)-.DELTA.9(12)-capnellene [Erratum to document cited in CA112(9):77599r] The Journal of Organic Chemistry. 55: 3966-3966. DOI: 10.1021/Jo00299A056 |
0.317 |
|
| 1990 |
Meyers AI, Wallace RH, Harre M, Garland R. The asymmetric synthesis of 2,2-dialkyl carboxylic esters and 2,2-disubstituted dihydronaphthalenes Journal of Organic Chemistry. 55: 3137-3143. DOI: 10.1021/Jo00297A032 |
0.463 |
|
| 1990 |
Meyers AI, Bienz S. Asymmetric total synthesis of (+)-.DELTA.9(12)-capnellene Journal of Organic Chemistry. 55: 791-798. DOI: 10.1021/Jo00290A005 |
0.546 |
|
| 1990 |
Warshawsky AM, Meyers AI. Asymmetric total synthesis of dibenzocyclooctadiene lignans (-)-schizandrin and (-)-isoschizandrin. Structure revision of (+)-isoschizandrin Journal of the American Chemical Society. 112: 8090-8099. DOI: 10.1021/Ja00178A037 |
0.476 |
|
| 1990 |
Gottlieb L, Meyers AI. Electrophilic formamidines. Organometallic addition to 2-methoxy pyrrolidine or piperidine N-t-butyl formamidines. Formation of 2-substituted pyrrolidines and piperidines Tetrahedron Letters. 31: 4723-4726. DOI: 10.1016/S0040-4039(00)97716-5 |
0.398 |
|
| 1990 |
Romo D, Romine JL, Midura W, Meyers A. Diastereoselective cyclopropanations of chiral bicyclic lactams leading to enantiomerically pure cyclopropanes. Application to the total synthesis of CIS-(1S, 3R)-deltamethrinic acid and R-(-)- dictyopterene C Tetrahedron. 46: 4951-4994. DOI: 10.1016/S0040-4020(01)85604-0 |
0.736 |
|
| 1990 |
Meyers AI, Guiles J. A convenient asymmetric synthesis of pyrrolo[2,1-a]isoquinolines Tetrahedron Letters. 31: 2813-2816. DOI: 10.1016/0040-4039(90)80155-F |
0.513 |
|
| 1990 |
Meyers AI, Bienz S. Asymmetric total synthesis of (+)-Δ9(12)-capnellene Journal of Organic Chemistry. 55: 791-798. |
0.414 |
|
| 1989 |
Meyers AI, Guiles J. The asymmetric total synthesis of (+)-reticuline Heterocycles. 28: 295-301. DOI: 10.3987/Com-88-S22 |
0.509 |
|
| 1989 |
Meyers AI, Berney D. Asymmetric synthesis of the (4aS,8aR,8S)-hydrolilolidone system. A formal total synthesis of unnatural (+)-aspidospermine The Journal of Organic Chemistry. 54: 4673-4676. DOI: 10.1021/Jo00280A040 |
0.35 |
|
| 1989 |
Meyers AI, Lefker BA, Sowin TJ, Westrum LJ. A facile synthesis of chiral bicyclic lactams utilized in the formation of chiral quaternary carbon compounds Journal of Organic Chemistry. 54: 4243-4246. DOI: 10.1021/Jo00278A053 |
0.477 |
|
| 1989 |
Meyers A, Busacca CA. An asymmetric route to fused carbocyclic systems via Diels-Alder reactions on chiral α,β-unsaturated bicyclic lactams Tetrahedron Letters. 30: 6977-6980. DOI: 10.1016/S0040-4039(01)93402-1 |
0.431 |
|
| 1989 |
Meyers AI, Busacca CA. Asymmetric Diels-Alder reactions of chiral α,β-unsaturated lactams Tetrahedron Letters. 30: 6973-6976. DOI: 10.1016/S0040-4039(01)93401-X |
0.449 |
|
| 1989 |
Gonzalez MA, Meyers AI. α-amino carbanions. A second generation formamidine for facile deprotonation leading to α-quaternary substitution Tetrahedron Letters. 30: 47-50. DOI: 10.1016/S0040-4039(01)80318-X |
0.362 |
|
| 1989 |
Gonzalez MA, Meyers AI. α-amino carbanions. A competition study to assess relative acidities in various formamidines Tetrahedron Letters. 30: 43-46. DOI: 10.1016/S0040-4039(01)80317-8 |
0.312 |
|
| 1989 |
Meyers A, Romo D. Chiral bicyclic lactams. An asymmetric synthesis of cis-(1s, 3r) deltamethrinic acid Tetrahedron Letters. 30: 1745-1748. DOI: 10.1016/S0040-4039(00)99569-8 |
0.75 |
|
| 1989 |
Meyers AI, Sturgess MA. The asymmetric total synthesis of (−)-dehydrovomifoliol. The penultimate precursor to (−)-abscisic acid (ABA) Tetrahedron Letters. 30: 1741-1744. DOI: 10.1016/S0040-4039(00)99568-6 |
0.458 |
|
| 1989 |
Meyers AI, Licini GM. Intramolecular asymmetric tandem additions to chiral naphthyl oxazolines Tetrahedron Letters. 30: 4049-4052. DOI: 10.1016/S0040-4039(00)99318-3 |
0.689 |
|
| 1989 |
Roth GP, Rithner CD, Meyers A. Asymmetric addition to chiral naphthalenes 5. An approach to the chlorothricolide system Tetrahedron. 45: 6949-6962. DOI: 10.1016/S0040-4020(01)89161-4 |
0.507 |
|
| 1988 |
Sowin TJ, Meyers AI. Enantioselective synthesis of the 1.beta.-methylcarbapenems via cycloaddition of 3-siloxypentadiene and 4-acetoxyazetidinone Journal of Organic Chemistry. 53: 4154-4156. DOI: 10.1021/Jo00252A067 |
0.359 |
|
| 1988 |
Andrews RC, Teague SJ, Meyers AI. Asymmetric total synthesis of (-)-podophyllotoxin Journal of the American Chemical Society. 110: 7854-7858. DOI: 10.1021/Ja00231A041 |
0.509 |
|
| 1988 |
Meyers AI, Romine JL, Fleming SA. A novel asymmetric synthesis of substituted cyclopropanes Journal of the American Chemical Society. 110: 7245-7247. DOI: 10.1021/Ja00229A067 |
0.764 |
|
| 1988 |
Pansegrau PD, Rieker WF, Meyers AI. The oxazoline-benzyne route to 1,2,3-trisubstituted benzenes. Tandem addition of organolithiums, organocuprates, and .alpha.-lithionitriles to benzynes Journal of the American Chemical Society. 110: 7178-7184. DOI: 10.1021/Ja00229A037 |
0.302 |
|
| 1988 |
Meyers AI, Miller DB, White FH. Chiral and achiral formamidines in synthesis. The first asymmetric route to (-)-yohimbine and an efficient total synthesis of (.+-.)-yohimbine Journal of the American Chemical Society. 110: 4778-4787. DOI: 10.1021/Ja00222A041 |
0.528 |
|
| 1988 |
Meyers AI, Roth GP, Hoyer D, Barner BA, Laucher D. Asymmetric tandem addition to chiral 1- and 2-substituted naphthalenes. Application to the synthesis of (+)-phyltetralin Journal of the American Chemical Society. 110: 4611-4624. DOI: 10.1021/Ja00222A021 |
0.358 |
|
| 1988 |
Meyers AI, Sturgess MA. Asymmetric synthesis of 4-alkoxy-4-alkylcyclohexen-2-ones. Application toward the synthesis of (+)-abscisic acid. Tetrahedron Letters. 29: 5339-5342. DOI: 10.1016/S0040-4039(00)82861-0 |
0.51 |
|
| 1988 |
Meyers AI, Brown JD. Stereoselective reduction of C=X by a chiral 1,4-dihydropyridine (NADH-MIMIC) in a self-immolative process Tetrahedron Letters. 29: 5617-5620. DOI: 10.1016/S0040-4039(00)80827-8 |
0.38 |
|
| 1988 |
Meyers AI, Lutomski KA, Laucher D. Regio- and stereoselective addition of organolithiums to naphthalenes. an efficient synthesis of 11,2-trisubstituted and trans-2-disubstituted dihydronaphthalenes Tetrahedron. 44: 3107-3118. DOI: 10.1016/S0040-4020(01)85942-1 |
0.494 |
|
| 1987 |
Meyers AI, Flisak JR, Aitken RA. An asymmetric synthesis of (-)-steganone : further application of chiral biaryl syntheses Journal of the American Chemical Society. 109: 5446-5452. DOI: 10.1021/Ja00252A022 |
0.521 |
|
| 1987 |
Meyers AI, Brown JD. The first nonenzymic stereospecific intramolecular reduction by an NADH mimic containing a covalently bound carbonyl moiety Journal of the American Chemical Society. 109: 3155-3156. DOI: 10.1021/Ja00244A054 |
0.37 |
|
| 1987 |
Meyers AI, Dickman DA. Absence of an isotope effect on the metalation of chiral formamidines. The mechanism of asymmetric alkylations leading to chiral amines Journal of the American Chemical Society. 109: 1263-1265. DOI: 10.1021/Ja00238A056 |
0.411 |
|
| 1987 |
Meyers AI, Brown JD, Laucher D. Asymmetric synthesis of 1,1,2- and 1,2-substituted dihydronaphthalenes via a chiral naphthyl imine Tetrahedron Letters. 28: 5283-5286. DOI: 10.1016/S0040-4039(00)96708-X |
0.444 |
|
| 1987 |
Meyers AI, Brown JD, Laucher D. Stereospecific conjugate addition of organolithium reagents to naphthylimines. A facile route to 1,1,2- and 1,2-substituted dihydroronaphthalenes Tetrahedron Letters. 28: 5279-5282. DOI: 10.1016/S0040-4039(00)96707-8 |
0.431 |
|
| 1987 |
Meyers A, Sowin TJ, Scholz S, Ueda Y. An efficient enantioselective synthesis of the carbapenam-2-one system. An approach to (+)-thienamycin and related carbapenems Tetrahedron Letters. 28: 5103-5106. DOI: 10.1016/S0040-4039(00)95602-8 |
0.514 |
|
| 1987 |
Meyers AI, Lefker BA. An efficient asymmetric synthesis of trisubstituted cyclohexenones and trisubstituted cyclopentenones from chiral 2,2-dialkyl 1,4- and 1,5-diketones Tetrahedron Letters. 28: 1745-1748. DOI: 10.1016/S0040-4039(00)95410-8 |
0.537 |
|
| 1987 |
Meyers AI, Lefker BA. An asymmetric synthesis of 4,4- and 6,6-dialkylcyclohexenones and 4,4- and 5,5-dialkylcyclopentenones. Application to the total synthesis of (-)-silphiperfol-6-ene Tetrahedron. 43: 5663-5676. DOI: 10.1016/S0040-4020(01)87745-0 |
0.552 |
|
| 1986 |
Meyers AI, Lawson JP, Walker DG, Linderman RJ. Synthetic studies on the streptogramin antibiotics. Enantioselective synthesis of the oxazole dienyl amine moiety Journal of Organic Chemistry. 51: 5111-5123. DOI: 10.1021/Jo00376A011 |
0.354 |
|
| 1986 |
Meyers AI, Sohda T, Loewe MF. An asymmetric synthesis and absolute configuration of (S)-(−)-deplancheine Journal of Organic Chemistry. 51: 3108-3112. DOI: 10.1021/Jo00366A005 |
0.426 |
|
| 1986 |
Meyers AI, Lefker BA, Wanner KT, Aitken RA. An asymmetric synthesis of chiral 4,4-disubstituted cyclohexenones in high enantiomeric purity Journal of Organic Chemistry. 51: 1936-1938. DOI: 10.1021/Jo00360A065 |
0.536 |
|
| 1986 |
Meyers AI, Lefker BA. Chiral bicyclic lactams for asymmetric synthesis of quaternary carbons. The total synthesis of (-)-.alpha.-cuparenone Journal of Organic Chemistry. 51: 1541-1544. DOI: 10.1021/Jo00359A030 |
0.457 |
|
| 1986 |
Meyers AI, Bailey TR. An asymmetric synthesis of (+)-morphinans in high enantiomeric purity Journal of Organic Chemistry. 51: 872-875. DOI: 10.1021/Jo00356A023 |
0.306 |
|
| 1986 |
Meyers AI, Barner BA. Asymmetric additions to chiral naphthalenes. III. The synthesis of (+)-trans-1,2-disubstituted-1,2-dihydronaphthalenes Journal of Organic Chemistry. 51: 120-122. DOI: 10.1021/Jo00351A034 |
0.438 |
|
| 1986 |
Meyers AI, Fleming SA. Efficient asymmetric (2 + 2) photocycloaddition leading to chiral cyclobutanes. Application to the total synthesis of (-)-grandisol Journal of the American Chemical Society. 108: 306-307. DOI: 10.1021/Ja00262A026 |
0.74 |
|
| 1986 |
Dickman DA, Meyers AI. An asymmetric synthesis of (+)-ocoteine Tetrahedron Letters. 27: 1465-1468. DOI: 10.1016/S0040-4039(00)84286-0 |
0.525 |
|
| 1986 |
Meyers AI, Lefker BA, Wanner KT, Aitken RA. An Asymmetric Synthesis of Chiral 4,4-Disubstituted Cyclohexenones in High Enantiomeric Purity. Cheminform. 17. DOI: 10.1002/Chin.198645147 |
0.536 |
|
| 1986 |
Meyers AI, Bailey TR. An Asymmetric Synthesis of (+)-Morphinans in High Enantiomeric Purity. Cheminform. 17. DOI: 10.1002/Chin.198634333 |
0.52 |
|
| 1986 |
MEYERS AI, FLEMING SA. ChemInform Abstract: Efficient Asymmetric [2 + 2] Photocycloaddition Leading to Chiral Cyclobutanes. Application to the Total Synthesis of (-)-Grandisol. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198620337 |
0.748 |
|
| 1986 |
Meyers AI, Hanreich R, Wanner KT. Efficient Asymmetrie Synthesis of (+)-Mesembrine and Related Chiral 4,4-Disubstituted Cyclohexanones. Cheminform. 17. DOI: 10.1002/Chin.198613324 |
0.489 |
|
| 1986 |
Meyers AI, Spohn RF, Linderman RJ. Enantioselective Synthesis of the Depsipeptide Unsaturated Acid Portion of Madumycin II. Cheminform. 17. DOI: 10.1002/Chin.198613086 |
0.424 |
|
| 1985 |
Meyers AI, Pansegrau PD. Tandem additions of cuprates to benzynes. A regioselective synthesis of 3-alkyl or aryl-2-substituted benzoic acids Journal of the Chemical Society, Chemical Communications. 690-691. DOI: 10.1039/C39850000690 |
0.506 |
|
| 1985 |
Meyers AI, Spohn RF, Linderman RJ. Enantioselective synthesis of the depsipeptide unsaturated acid portion of madumycin II Journal of Organic Chemistry. 50: 3633-3635. DOI: 10.1021/Jo00219A042 |
0.424 |
|
| 1985 |
Meyers AI, Dickman DA, Bailey TR. Asymmetric synthesis of 2-alkyl pyrrolidines and piperidines. Synthesis of (+)-metazocine Journal of the American Chemical Society. 107: 7974-7978. DOI: 10.1021/Ja00312A029 |
0.54 |
|
| 1985 |
Meyers AI, Hanreich R, Wanner KT. An efficient asymmetric synthesis of (+)-mesembrine and related chiral 4,4-disubstituted cyclohexenones Journal of the American Chemical Society. 107: 7776-7778. DOI: 10.1021/Ja00311A100 |
0.502 |
|
| 1985 |
Meyers AI, Himmelsbach RJ. An enantioselective synthesis of 2,2',6-trisubstituted biphenyls Journal of the American Chemical Society. 107: 682-685. DOI: 10.1021/Ja00289A023 |
0.37 |
|
| 1985 |
Loewe MF, Boes M, Meyers AI. A mechanistic model for asymmetric alkylation of chiral dipole stabilized anions Tetrahedron Letters. 26: 3295-3298. DOI: 10.1016/S0040-4039(00)98281-9 |
0.484 |
|
| 1985 |
Loewe MF, Meyers AI. An asymmetric synthesis of indole alkaloids Tetrahedron Letters. 26: 3291-3294. DOI: 10.1016/S0040-4039(00)98280-7 |
0.487 |
|
| 1985 |
Meyers AI, Marra JM. Formamidines as α-amino carbanion precursors. The synthesis of 2-arylpiperidines, -pyrrolidines, and nicotine analogs Tetrahedron Letters. 26: 5863-5866. DOI: 10.1016/S0040-4039(00)98247-9 |
0.404 |
|
| 1985 |
Meyers AI, Hoyer D. Stereochemistry of the Ph3P-CCl4 mediated cyclization of carboxylic acids and 1,2-amino alcohols (Vorbruggen Method) Tetrahedron Letters. 26: 4687-4690. DOI: 10.1016/S0040-4039(00)94924-4 |
0.328 |
|
| 1985 |
Meyers A, Wanner KT. Chiral quaternary carbon compounds. II. An asymmetric synthesis of (R) or (S)-4,4-dialkyl-2-cyclopentenones Tetrahedron Letters. 26: 2047-2050. DOI: 10.1016/S0040-4039(00)94775-0 |
0.492 |
|
| 1985 |
Meyers AI, Walkup RD. Diastereofacial selectivity via aldol reactions using ethyl dithioacetate and ethyl dithiopropionate enolates Tetrahedron. 41: 5089-5106. DOI: 10.1016/S0040-4020(01)96754-7 |
0.387 |
|
| 1985 |
Reuman M, Meyers AI. The synthetic utility of oxazolines in aromatic substitution Tetrahedron. 41: 837-860. DOI: 10.1016/S0040-4020(01)96401-4 |
0.468 |
|
| 1985 |
Meyers AI, Pansegrau PD. Tandem Additions Of Cuprates To Benzynes. A Regioselective Synthesis Of 3-Alkyl Or Aryl-2-Substituted Benzoic Acids Cheminform. 16. DOI: 10.1002/Chin.198537196 |
0.52 |
|
| 1985 |
Meyers AI, Edwards PD, Bailey TR, Jagdmann GEJ. α-AMINO CARBANIONS. PREPARATION, METALATION, AND ALKYLATION OF ENAMIDINES. SYNTHESIS OF PIPERIDINE AND PYRROLIDINE NATURAL PRODUCTS AND HOMOLOGATION OF CARBONYL COMPOUNDS Cheminform. 16. DOI: 10.1002/Chin.198535204 |
0.436 |
|
| 1985 |
Meyers AI, Himmelsbach RJ. An Enantioselective Synthesis Of 2,2′,6-Trisubstituted Biphenyls Cheminform. 16. DOI: 10.1002/Chin.198524176 |
0.539 |
|
| 1984 |
Pirkle WH, Welch CJ, Mahler GS, Meyers AI, Fuentes LM, Boes M. Chromatographic separation of the enantiomers of N-acylated heterocyclic amines The Journal of Organic Chemistry. 49: 2504-2506. DOI: 10.1021/Jo00187A043 |
0.337 |
|
| 1984 |
Meyers AI, Edwards PD, Rieker WF, Bailey TR. .alpha.-Amino carbanions via formamidines. Alkylation of pyrrolidines, piperidines, and related heterocycles Journal of the American Chemical Society. 106: 3270-3276. DOI: 10.1021/Ja00323A035 |
0.309 |
|
| 1984 |
Barner BA, Meyers AI. Asymmetric addition to chiral naphthyloxazolines. A facile route to 1,1,2-trisubstituted 1,2-dihydronaphthalenes in high enantiomeric excess Journal of the American Chemical Society. 106: 1865-1866. DOI: 10.1021/Ja00318A067 |
0.479 |
|
| 1984 |
Meyers AI, Harre M, Garland R. Asymmetric synthesis of quaternary carbon centers Journal of the American Chemical Society. 106: 1146-1148. DOI: 10.1021/Ja00316A071 |
0.322 |
|
| 1984 |
Meyers AI, Pansegrau PD. Tandem addition-rearrangement of nitrile anions to benzyne. A convenient synthesis of 3-cyano-2-alkyl benzoic acids and benzaldehydes. Tetrahedron Letters. 25: 2941-2944. DOI: 10.1016/S0040-4039(01)81332-0 |
0.517 |
|
| 1984 |
Meyers AI, Loewe MF. The N-9, C-1 dianion of tetrahydro-β-carbolines. Regioselective alkylation leading to indole alkaloid systems Tetrahedron Letters. 25: 2641-2644. DOI: 10.1016/S0040-4039(01)81251-X |
0.311 |
|
| 1984 |
Edwards PD, Meyers AI. A convenient synthesis of 1-azabicycloalkanes and their lactams via cuprates of formamidines Tetrahedron Letters. 25: 939-942. DOI: 10.1016/S0040-4039(01)80067-8 |
0.458 |
|
| 1984 |
Meyers AI, Fuentes LM, Kubota Y. ENANTIOSELECTIVE ALKYLATION OF α-AMINO CARBANIONS. THE SYNTHESIS OF (S)-1-ALKYL-1,2,3,4 TETRAHYDROISOQUINOLINES Tetrahedron. 40: 1361-1370. DOI: 10.1016/S0040-4020(01)82421-2 |
0.514 |
|
| 1984 |
Meyers AI, Hoyer D. Asymmetric tandem additions to chiral 2-naphthyloxazolines. The synthesis of enantiomerically pure 1,2,2-trisubstituted- 1,2-dihydronaphthalenes Tetrahedron Letters. 25: 3667-3670. DOI: 10.1016/0040-4039(84)80100-8 |
0.424 |
|
| 1984 |
Meyers A, Yamamoto Y. Stereoselectivity in the aldol reaction Tetrahedron. 40: 2309-2315. DOI: 10.1016/0040-4020(84)80014-9 |
0.464 |
|
| 1984 |
Pirkle WH, Welch CJ, Mahler GS, Meyers AI, Fuentes LM, Boes M. Chromatographic Separation Of The Enantiomers Of N-Acylated Heterocyclic Amines Cheminform. 15. DOI: 10.1002/Chin.198449061 |
0.337 |
|
| 1984 |
Meyers AI, Boes M, Dickman DA. High Enantioselective Alkyation Of Tetrahydroisoquinolines With A Chiral Valinol Derivative As Auxilliary Reagent; Asymmetric Synthesis Of (S)-Isoquinoline Alkaloids Cheminform. 15. DOI: 10.1002/Chin.198440313 |
0.531 |
|
| 1984 |
Meyers AI, Edwards PD, Rieker WF, Bailey TR. α-AMINO CARBANIONS VIA FORMAMIDINES. ALKYLATION OF PYRROLIDINES, PIPERIDINES, AND RELATED HETEROCYCLES Cheminform. 15. DOI: 10.1002/Chin.198436102 |
0.38 |
|
| 1984 |
Barner BA, Meyers AI. Asymmetric addition to chiral naphthyloxazolines. A facile route to 1,1,2-trisubstituted 1,2-dihydronaphthalenes in high enantiomeric excess Cheminform. 15. DOI: 10.1002/Chin.198426087 |
0.479 |
|
| 1984 |
Meyers AI, Wettlaufer DG. The complete intramolecular transfer of a central chiral element to an axial chiral element. Oxidation of (S)-4-naphthyldihydroquinolines to (S)-4-naphthylquinolines Journal of the American Chemical Society. 106: 1135-1136. DOI: 10.1002/Chin.198421223 |
0.316 |
|
| 1984 |
Meyers AI, Harre M, Garland R. Asymmetric Synthesis Of Quaternary Carbon Centers Cheminform. 15. DOI: 10.1002/Chin.198421097 |
0.394 |
|
| 1984 |
Meyers AI, Himmelsbach RJ, Reuman M. Reductive Cleavage Of Aryl Oxazolines To Benzaldehydes And Substituted Toluenes Cheminform. 15. DOI: 10.1002/Chin.198414119 |
0.474 |
|
| 1984 |
Meyers AI, Boes M, Dickman DA. Highly Enantioselective Alkylation of Tetrahydroisoquinolines via a Valine Chiral Auxiliary; Asymmetric Synthesis of (S)‐Isoquinoline Alkaloids Angewandte Chemie. 23: 458-459. DOI: 10.1002/Anie.198404581 |
0.534 |
|
| 1984 |
Meyers A, Boes M, Dickman DA. Hochenantioselektive Alkylierung von Tetrahydroisochinolinen mit einem Valinolderivat als Hilfsreagens: asymmetrische Synthese von (S)-Isochinolinalkaloiden Angewandte Chemie. 96: 448-449. DOI: 10.1002/Ange.19840960627 |
0.315 |
|
| 1983 |
Meyers AI, Lutomski KA. Substitutions on 1-Methoxynaphthalenes via their Oxazoline Derivatives: A Convenient Route to 1-Substituted Naphthoic Acids Synthesis. 1983: 105-107. DOI: 10.1055/S-1983-30235 |
0.434 |
|
| 1983 |
Meyers AI, Himmelsbach RJ, Reuman M. Reductive cleavage of aryl oxazolines to benzaldehydes and substituted toluenes Journal of Organic Chemistry. 48: 4053-4058. DOI: 10.1021/Jo00170A036 |
0.305 |
|
| 1983 |
Meyers AI, Fuentes LM. Asymmetric alkylation of α-amino carbanions. An enantioselective synthesis of (S)-1-alkyl-1,2,3,4-tetrahydroisoquinolines Journal of the American Chemical Society. 105: 117-118. DOI: 10.1021/Ja00339A022 |
0.503 |
|
| 1983 |
Meyers AI, Pansegrau PD. The synthesis of 1,2,3-trisubstituted benzenes. Further comments on benzynes derived from aryl oxazolines Tetrahedron Letters. 24: 4935-4938. DOI: 10.1016/S0040-4039(01)99815-6 |
0.496 |
|
| 1983 |
Kirk Smith J, Newcomb M, Bergbreiter DE, Williams DR, Meyers A. Highly regioselective deprotonations of acyclic ketimines Tetrahedron Letters. 24: 3559-3562. DOI: 10.1016/S0040-4039(00)88167-8 |
0.409 |
|
| 1983 |
Meyers AI, White SK, Fuentes LM. Determination of enantiomeric composition of chiral 2-substituted-1,2-glycols via 13C-NMR and HPLC Tetrahedron Letters. 24: 3551-3554. DOI: 10.1016/S0040-4039(00)88165-4 |
0.394 |
|
| 1983 |
Linderman RJ, Meyers AI. N-alkyl-β-aminoethylphosphonium salts. Useful reagents for the synthesis of 2° allylamines Tetrahedron Letters. 24: 3043-3046. DOI: 10.1016/S0040-4039(00)88090-9 |
0.395 |
|
| 1983 |
Meyers AI, Hanagan MA, Trefonas LM, Baker RJ. An asymmetric synthesis of chiral phthalides via chiral lithiated oxazolines Tetrahedron. 39: 1991-1999. DOI: 10.1016/S0040-4020(01)91917-9 |
0.536 |
|
| 1982 |
Meyers AI, Natale NR. Regioselective Additions to 3-(Oxazolinyl)pyridine with Organolithium Reagents. Cheminform. 13: 13. DOI: 10.3987/S(B)-1982-01-0013 |
0.501 |
|
| 1982 |
Meyers AI, Gabel RA. Substitutions of pyridines activated by oxazolines via nucleophilic additions for metalation-alkylation Journal of Organic Chemistry. 13: 2633-2637. DOI: 10.1021/Jo00134A024 |
0.351 |
|
| 1982 |
Meyers AI, Hellring S. A novel entry into indole alkaloids Journal of Organic Chemistry. 13: 2229-2231. DOI: 10.1021/Jo00132A063 |
0.368 |
|
| 1982 |
Meyers AI, Lutomski KA. Enantioselective synthesis of binaphthyls via nucleophilic aromatic substitution on chiral oxazolines Journal of the American Chemical Society. 104: 879-881. DOI: 10.1021/Ja00367A053 |
0.57 |
|
| 1982 |
Meyers AI, Rieker W. Benzyne derived from aryloxazolines. A versatile intermediate. Tetrahedron Letters. 23: 2091-2094. DOI: 10.1016/S0040-4039(00)87269-X |
0.322 |
|
| 1981 |
Meyers AI, Avila WB. Chemistry of aryloxazolines. Applications to the synthesis of lignan lactone derivatives The Journal of Organic Chemistry. 46: 3881-3886. DOI: 10.1021/Jo00332A024 |
0.452 |
|
| 1981 |
Meyers AI, Lawson JP, Carver DR. Highly stereoselective route to (E)-allyl amines via vinyltri-n-butylphosphonium salts (Schweizer reaction) Journal of Organic Chemistry. 12: 3119-3123. DOI: 10.1021/Jo00328A027 |
0.378 |
|
| 1981 |
Meyers AI, Reuman M, Gabel RA. Nucleophilic annulations of aromatics. Novel route to benzo-fused ring systems via oxazoline activation Journal of Organic Chemistry. 12: 783-788. DOI: 10.1021/Jo00317A027 |
0.343 |
|
| 1981 |
Meyers AI, Yamamoto Y. Enantioselective aldol reactions with high threo or erythro selectivity using boron azaenolates Journal of the American Chemical Society. 103: 4278-4279. DOI: 10.1021/Ja00404A064 |
0.374 |
|
| 1981 |
Meyers AI, Williams DR, White S, Erickson GW. An asymmetric synthesis of acyclic and macrocyclic .alpha.-alkyl ketones. The role of (e)- and (z)-lithioenamines Journal of the American Chemical Society. 103: 3088-3093. DOI: 10.1021/Ja00401A029 |
0.38 |
|
| 1981 |
Meyers AI, Williams DR, Erickson GW, White S, Druelinger M. Enantioselective alkylation of ketones via chiral, nonracemic lithioenamines. An asymmetric synthesis of .alpha.-alkyl and .alpha.,.alpha.'-dialkyl cyclic ketones Journal of the American Chemical Society. 103: 3081-3087. DOI: 10.1021/Ja00401A028 |
0.351 |
|
| 1981 |
Meyers A, Natale NR, Wettlaufer DG, Rafii S, Clardy J. Chiral 1,4-dihydropyridines. Synthesis and absolute configuration. Tetrahedron Letters. 22: 5123-5126. DOI: 10.1016/S0040-4039(01)92436-0 |
0.447 |
|
| 1981 |
Meyers AI, Hellring S, Hoeve WT. Dipole stabilized α-amino carbanions. II. Alkylation of tetrahydroisoquinolines in the 1-position. Tetrahedron Letters. 22: 5115-5118. DOI: 10.1016/S0040-4039(01)92434-7 |
0.386 |
|
| 1981 |
Meyers AI, Hudspeth JP. Enantioselective synthesis of C3-C10 fragment (northeastern zone) of maytansinoids with 4-chiral centers (4S,5S,6R,7S) Tetrahedron Letters. 22: 3925-3928. DOI: 10.1016/S0040-4039(01)82028-1 |
0.494 |
|
| 1981 |
MEYERS AI, YAMAMOTO Y. ChemInform Abstract: ENANTIOSELECTIVE ALDOL REACTIONS WITH HIGH THREO OR ERYTHRO SELECTIVITY USING BORON AZAENOLATES Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198143071 |
0.398 |
|
| 1981 |
Meyers AI, Hanagan MA, Mazzu AL. 2-Oxazolines From Amides Via Imidates Cheminform. 12: 361. DOI: 10.1002/Chin.198121212 |
0.378 |
|
| 1981 |
Meyers AI, Reider PJ, Campbell AL. Total Synthesis Of (.+-.)-Maytansinol. The Common Precursor To The Maytansinoids Cheminform. 12. DOI: 10.1002/Chin.198103311 |
0.48 |
|
| 1980 |
Meyers AI, Slade J. Resolution of .alpha.-substituted mandelic acids via chiral oxazolines using pressurized chromatography The Journal of Organic Chemistry. 45: 2912-2914. DOI: 10.1021/Jo01302A033 |
0.349 |
|
| 1980 |
Meyers AI, Yamamoto Y, Mihelich ED, Bell RA. Asymmetric synthesis of 2-substituted butyrolactones and valerolactones Journal of Organic Chemistry. 11: 2792-2796. DOI: 10.1021/Jo01302A009 |
0.548 |
|
| 1980 |
Meyers AI, Slade J. Asymmetric addition of organometallics to chiral ketooxazolines. Preparation of enantiomerically enriched .alpha.-hydroxy acids Journal of Organic Chemistry. 11: 2785-2791. DOI: 10.1021/Jo01302A008 |
0.404 |
|
| 1980 |
Meyers AI, Reider PJ, Campbell AL. Total Synthesis of (±)-Maytansinol. The Common Precursor to the Maytansinoids Journal of the American Chemical Society. 102: 6597-6598. DOI: 10.1021/Ja00541A054 |
0.322 |
|
| 1980 |
Meyers AI, Amos RA. Studies directed toward the total synthesis of streptogramin antibiotics. Enantiospecific approach to the nine-membered macrocycle of griseoviridin Journal of the American Chemical Society. 102: 870-872. DOI: 10.1021/Ja00522A085 |
0.388 |
|
| 1980 |
Meyers AI, Comins DL, Roland DM, Henning R, Shimizu K. Total Synthesis Of (.+‐.)‐Maysine Cheminform. 11. DOI: 10.1002/Chin.198007349 |
0.478 |
|
| 1979 |
Meyers AI. Asymmetric carbon-carbon bond forming reactions Pure and Applied Chemistry. 51: 1255-1268. DOI: 10.1351/Pac197951061255 |
0.492 |
|
| 1979 |
Meyers AI, Brich Z. 1 H n.m.r. determination of enantiomeric purities of 2-substituted aldehydes via the aldimine of 2-amino-1-methoxymenth-8-ene Journal of the Chemical Society, Chemical Communications. 567-568. DOI: 10.1039/C39790000567 |
0.342 |
|
| 1979 |
Meyers AI, Brich Z, Erickson GW, Traynor SG. Asymmetric syntheses from terpene alkanolamines. Formation of optically active 2-methyloctanal Journal of the Chemical Society, Chemical Communications. 566-567. DOI: 10.1039/C39790000566 |
0.402 |
|
| 1979 |
Meyers AI, Smith RK, Whitten CE. Highly stereoselective addition of organolithium reagents to chiral oxazolines. Asymmetric synthesis of 3-substituted alkanoic acids and 3-substituted lactones Journal of Organic Chemistry. 10: 2250-2256. DOI: 10.1021/Jo01327A046 |
0.562 |
|
| 1979 |
Meyers AI, Roland DM, Comins DL, Henning R, Fleming MP, Shimizu K. Progress toward the total synthesis of maytansinoids. Synthesis of (.+-.)-4,5-deoxymaysine (N-methylmaysenine) Journal of the American Chemical Society. 101: 4732-4734. DOI: 10.1021/Ja00510A051 |
0.442 |
|
| 1979 |
Meyers AI, Reider PJ. Stereoselective Synthesis of threo-3-Hydroxy-2-methylcarboxylic Acids Using Alkoxyalkyl Propionates Journal of the American Chemical Society. 101: 2501-2502. DOI: 10.1021/Ja00503A052 |
0.464 |
|
| 1979 |
Meyers AI, Babiak KA, Campbell AL, Comins DL, Fleming MP, Henning R, Heuschmann M, Hudspeth JP, Kane JM. Total synthesis of (-)-maysine Journal of the American Chemical Society. 105: 5015-5024. DOI: 10.1021/Ja00353A027 |
0.478 |
|
| 1979 |
Meyers AI, Campbell AL. 2-aryl acetals as acyl anion equivalents Tetrahedron Letters. 20: 4155-4158. DOI: 10.1016/S0040-4039(01)86531-X |
0.354 |
|
| 1979 |
Meyers AI, Smith RK. A total asymmetric synthesis of (+)-ar-turmerone Tetrahedron Letters. 20: 2749-2752. DOI: 10.1016/S0040-4039(01)86405-4 |
0.5 |
|
| 1979 |
MEYERS AI, ROLAND DM, COMINS DL, HENNING R, FLEMING MP, SHIMIZU K. ChemInform Abstract: PROGRESS TOWARD THE TOTAL SYNTHESIS OF MAYTANSINOIDS. SYNTHESIS OF (.+-.)-4,5-DEOXYMAYSINE (N-METHYLMAYSENINE) Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197947336 |
0.648 |
|
| 1979 |
Meyers AI, Reider PJ. Stereoselective Synthesis Of Threo-3-Hydroxy-2-Methylcarboxylic Acids Using Alkoxyalkyl Propionates Cheminform. 10. DOI: 10.1002/Chin.197932187 |
0.464 |
|
| 1979 |
Meyers AI, Tomioka K, Fleming MP. CONVENIENT PREPARATION OF α,β-UNSATURATED ALDEHYDES Cheminform. 10. DOI: 10.1002/Chin.197905160 |
0.314 |
|
| 1978 |
Meyers AI, Gabel RA. Oxazolines as Activating Groups in Aromatic Substitution. Selective Metalation or Addition to the 4-Position of Pyridine. A New Synthesis of 1,4-Dihydropyridines Heterocycles. 11: 133. DOI: 10.3987/S(N)-1978-01-0133 |
0.391 |
|
| 1978 |
COMINS D, MEYERS AI. A Facile and Efficient Formylation of Grignard Reagents Synthesis. 1978: 403-404. DOI: 10.1055/S-1978-24767 |
0.582 |
|
| 1978 |
Meyers AI, Williams DR. Asymmetric alkylation of acyclic ketones via chiral metallo enamines. Effect of kinetic vs. thermodynamic metalations. Journal of Organic Chemistry. 43: 3245-3247. DOI: 10.1021/Jo00410A034 |
0.4 |
|
| 1978 |
Meyers AI, Poindexter GS, Brich Z. Asymmetric synthesis of (+)- or (-)-2-methyloctanal via the metalloenamines of chiral alkoxy amines Journal of Organic Chemistry. 43: 892-898. DOI: 10.1021/Jo00399A021 |
0.553 |
|
| 1978 |
Meyers A, Tomioka K, Roland DM, Comins D. Progress toward the total synthesis of maytansinoids. An efficient route to two major precursors (western-southern zone) Tetrahedron Letters. 19: 1375-1378. DOI: 10.1016/S0040-4039(01)94549-6 |
0.629 |
|
| 1978 |
Meyers AI, Comins DL. N-methylamino pyridyl amides (mapa) II. An efficient acylating agent for various nucleophiles and sequential addition to unsymmetrical tert-alcohols Tetrahedron Letters. 19: 5179-5182. DOI: 10.1016/S0040-4039(01)85843-3 |
0.548 |
|
| 1978 |
Meyers AI, Tait TA, Comins DL. The use of dithioesters as acyl anion equivalents. Double homologation of the synthon Tetrahedron Letters. 19: 4657-4660. DOI: 10.1016/S0040-4039(01)85697-5 |
0.526 |
|
| 1978 |
Meyers AI, Gabel RA. Oxazolines as activating groups in aromatic substitution. Regioselective metallation of the 3-position in pyridine. Tetrahedron Letters. 19: 227-230. DOI: 10.1016/S0040-4039(01)85090-5 |
0.31 |
|
| 1978 |
Meyers AI, Williams BE. Oxazolines as activating groups in aromatic substitution. Nucleophilic displacement of o-fluoro substituents by organometallics and lithio amides Tetrahedron Letters. 19: 223-226. DOI: 10.1016/S0040-4039(01)85089-9 |
0.34 |
|
| 1977 |
Kane JM, Meyers AI. Progress toward the total synthesis of maytansinoids. A facile route to the aromatic moiety (western zone) Tetrahedron Letters. 18: 771-774. DOI: 10.1016/S0040-4039(01)92750-9 |
0.461 |
|
| 1977 |
Lown J, Majumdar KC, Meyers AI, Hecht A. Studies related to antitumor antibiotics Bioorganic Chemistry. 6: 453-463. DOI: 10.1016/0045-2068(77)90044-X |
0.337 |
|
| 1977 |
Meyers AI, Mazzu A, Whitten CE. Chiral Oxazolines In Asymmetric Synthesis. Effect Of Substituents On Asymmetric Induction Cheminform. 6: 971. DOI: 10.1002/Chin.197746115 |
0.533 |
|
| 1976 |
Meyers AI, Ford ME. Oxazolines. XX. Synthesis of achiral and chiral thiiranes and olefins by reaction of carbonyl compounds with 2-(alkylthio)-2-oxazolines Journal of Organic Chemistry. 41: 1735-1742. DOI: 10.1021/Jo00872A015 |
0.497 |
|
| 1976 |
Meyers AI, Williams DR, Druelinger M. Enantioselective alkylation of cyclohexanone via chiral lithio-chelated enamines Journal of the American Chemical Society. 98: 3032-3033. DOI: 10.1021/Ja00426A068 |
0.493 |
|
| 1976 |
Meyers AI, Kamata K. Oxazolines. XXI. Kinetic resolution of sec-alkyl halides and simultaneous asymmetric synthesis of 3-alkylalkanoic acids using a chiral oxazoline. A method for determining absolute configurations and maximum optical rotations Journal of the American Chemical Society. 98: 2290-2294. DOI: 10.1021/JA00424A049 |
0.344 |
|
| 1976 |
Meyers AI, Knaus G, Kamata K, Ford ME. Asymmetric synthesis of R and S .alpha.-alkylalkanoic acids from metalation and alkylation of chiral 2-oxazolines Journal of the American Chemical Society. 98: 567-576. DOI: 10.1021/Ja00418A041 |
0.408 |
|
| 1976 |
Meyers AI, Whitten CE. An asymmetric synthesis of 5-methoxy-3-substituted acids and their related lactones in high enantiomeric purity Tetrahedron Letters. 17: 1947-1950. DOI: 10.1016/S0040-4039(00)78086-5 |
0.498 |
|
| 1976 |
Meyers AI, Slade J. A Convenient Synthesis and Resolution of R- and S- Atrolactic Acid in High Enantiomeric Purity Cheminform. 8: 601-608. DOI: 10.1002/Chin.197725114 |
0.444 |
|
| 1976 |
Meyers AI, Whitten CE. Oxazolines. Xxiv- Chiral Oxazolines And Thiazolines From L-Serine And L-Cysteine. Their Potential Use In Asymmetric Synthesis Cheminform. 4: 1687. DOI: 10.1002/Chin.197709242 |
0.336 |
|
| 1976 |
Meyers AI, Whitten CE. Oxazolines. XIX. Asymmetric synthesis of 3-substituted alkanoic acids via conjugated addition of organolithium reagents to chiral oxazolines Cheminform. 7. DOI: 10.1002/Chin.197601145 |
0.547 |
|
| 1976 |
Meyers AI, Mihelich ED. The Synthetic Utility of 2‐Oxazolines Angewandte Chemie. 15: 270-281. DOI: 10.1002/Anie.197602701 |
0.522 |
|
| 1976 |
Meyers AI, Mihelich ED. Die Nützlichkeit der 2‐Oxazoline in der Synthese Angewandte Chemie. 88: 321-332. DOI: 10.1002/Ange.19760881004 |
0.321 |
|
| 1975 |
Meyers AI, Mihelich ED. Oxazolines. XVII. Regioselective metalation of 2-aryl oxazolines. Route to polydeuteriobenzoic acids Journal of Organic Chemistry. 40: 3158-3159. DOI: 10.1021/Jo00909A040 |
0.336 |
|
| 1975 |
Meyers AI, Durandetta JL, Munavu R. 2-Thiazolines in organic synthesis. Formation of .beta.-hydroxy aldehydes with protected hydroxy groups. Synthesis of homoallylic alcohols Journal of Organic Chemistry. 40: 2025-2029. DOI: 10.1021/Jo00902A002 |
0.332 |
|
| 1975 |
Meyers AI, Durandetta JL. 2-Thiazolines in organic synthesis. Synthesis of mono-, di-, and trialkylacetaldehydes Journal of Organic Chemistry. 40: 2021-2025. DOI: 10.1021/Jo00902A001 |
0.442 |
|
| 1975 |
Meyers AI, Mihelich ED. Asymmetric synthesis of 2-substituted .gamma.-butyrolactones and 2-substituted 1,4-butanediols Journal of Organic Chemistry. 40: 1186-1187. DOI: 10.1021/Jo00896A049 |
0.495 |
|
| 1975 |
Stout DM, Takaya T, Meyers AI. Unequivocal synthesis of N-substituted 1,4-dihydropyridines The Journal of Organic Chemistry. 40: 563-569. DOI: 10.1021/Jo00893A005 |
0.424 |
|
| 1975 |
Meyers AI, Mihelich ED. Oxazolines. XXII. Nucleophilic aromatic substitution on aryl oxazolines. Efficient approach to unsymmetrically substituted biphenyls and o-alkyl benzoic acids Journal of the American Chemical Society. 97: 7383-7385. DOI: 10.1021/Ja00858A034 |
0.424 |
|
| 1975 |
Meyers AI, Whitten CE. Oxazolines. XIX. Asymmetric synthesis of 3-substituted alkanoic acids via conjugated addition of organolithium reagents to chiral oxazolines Journal of the American Chemical Society. 97: 6266-6267. DOI: 10.1021/Ja00854A065 |
0.547 |
|
| 1975 |
Meyers AI, Ford ME. Synthesis via oxazolines - one carbon homologation of aldehydes and ketones to thiiranes and olefins Tetrahedron Letters. 16: 2861-2864. DOI: 10.1016/S0040-4039(00)75015-5 |
0.429 |
|
| 1975 |
Meyers AI, Brinkmeyer RS. Progress toward the total synthesis of maytansine. A model system containing the C-7 to C-16 moiety (southern and eastern zone) Tetrahedron Letters. 16: 1749-1752. DOI: 10.1016/S0040-4039(00)72250-7 |
0.319 |
|
| 1975 |
Meyers AI, Shaw CC, Horne D, Trefonas LM, Majeste RJ. Progress toward the total synthesis of maytansine. A stereoselective synthesis of the C-1 to C-7 moiety (northern zone) Tetrahedron Letters. 16: 1745-1748. DOI: 10.1016/S0040-4039(00)72249-0 |
0.406 |
|
| 1975 |
Meyers AI, Durandetta JL. 2‐Thiazolines In Organic Synthesis, A Synthesis Of Mono‐, Di‐, And Trialkylacetaldehydes Cheminform. 6. DOI: 10.1002/Chin.197542176 |
0.341 |
|
| 1975 |
STOUT DM, TAKAYA T, MEYERS AI. ChemInform Abstract: AN UNEQUIVOCAL SYNTHESIS OF N-SUBSTITUTED 1,4-DIHYDROPYRIDINES Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/chin.197523317 |
0.335 |
|
| 1975 |
Meyers AI, Mihelich ED, Kamata K. Synthesis Via Oxazolines, A Highly Stereoselective Synthesis Of (+-)-Cis-2-Methyl Cyclopentanecarboxylic Acid, Via A Kinetically Controlled Cyclization Cheminform. 6. DOI: 10.1002/Chin.197501178 |
0.464 |
|
| 1974 |
Meyers AI, Mihelich ED, Kamata K. Synthesis via oxazolines. A highly stereoselective synthesis of (±)-cis-2-methyl cyclopentanecarboxylic acid, via a kinetically controlled cyclization Journal of the Chemical Society, Chemical Communications. 768-769. DOI: 10.1039/C39740000768 |
0.405 |
|
| 1974 |
Meyers AI, Temple DL, Haidukewych D, Mihelich ED. Oxazolines. XI. Synthesis of functionalized aromatic and aliphatic acids. Useful protecting group for carboxylic acids against Grignard and hydride reagents Journal of Organic Chemistry. 39: 2787-2793. DOI: 10.1021/Jo00932A024 |
0.388 |
|
| 1974 |
Meyers AI, Mihelich ED, Nolen RL. Oxazolines. X. Synthesis of .gamma.-butyrolactones Journal of Organic Chemistry. 39: 2783-2787. DOI: 10.1021/Jo00932A023 |
0.316 |
|
| 1974 |
Meyers AI, Temple DL, Nolen RL, Mihelich ED. Oxazolines. IX. Synthesis of homologated acetic acids and esters Journal of Organic Chemistry. 39: 2778-2783. DOI: 10.1021/Jo00932A022 |
0.439 |
|
| 1974 |
Narwid TA, Meyers AI. Chemistry of dihydro-1,3-oxazines. 24. Formation of pyrroles from dihydro-1,3-oxazines The Journal of Organic Chemistry. 39: 2572-2574. DOI: 10.1021/Jo00931A026 |
0.344 |
|
| 1974 |
Malone GR, Meyers AI. Reaction of lithiated oxazines with esters and nitriles Journal of Organic Chemistry. 39: 713-714. DOI: 10.1021/Jo00919A029 |
0.358 |
|
| 1974 |
Malone GR, Meyers AI. 5,6-Dihydro-1,3-oxazines. XXIII. Chemistry of 2-chloromethyloxazines. Formation of phosphoranes and phosphonates. Use of .alpha.,.beta. unsaturated oxazines as a common intermediate for the synthesis of aldehydes, ketones, and acids Journal of Organic Chemistry. 39: 623-628. DOI: 10.1021/Jo00919A009 |
0.386 |
|
| 1974 |
Malone GR, Meyers AI. Chemistry of 1,6-dihydro-1,3-oxazines. XXII. Chemistry of 2-chloromethyl-5,6-dihydro-1,3-oxazines. Grignard coupling and metalation studies. Synthesis of .alpha.-chloroaldehydes and arylacetic acids Journal of Organic Chemistry. 39: 618-623. DOI: 10.1021/Jo00919A008 |
0.365 |
|
| 1974 |
Meyers AI, Knaus G. Oxazolines. XIV. Asymmetric synthesis of R and S dialkylacetic acids from a single chiral oxazoline Journal of the American Chemical Society. 96: 6508-6510. DOI: 10.1021/Ja00827A041 |
0.436 |
|
| 1974 |
Meyers AI, Knaus G, Kamata K. Synthesis via 2-oxazolines. IV. Asymmetric synthesis of 2-methylalkanoic acids from a chiral oxazoline Journal of the American Chemical Society. 96: 268-270. DOI: 10.1021/Ja00808A054 |
0.535 |
|
| 1974 |
Meyers AI, Knaus G, Kendall PM. Synthesis via oxazolines IX. An asymmetric synthesis of 2-methoxy and 2-chloroalkanoic acids Tetrahedron Letters. 15: 3495-3498. DOI: 10.1016/S0040-4039(01)91946-X |
0.501 |
|
| 1974 |
Meyers AI, Ford ME. Synthesis via oxazolines. VIII. Asymmetric addition of grignard reagents to carbonyl compounds in the presence of a chiral oxazoline Tetrahedron Letters. 15: 1341-1344. DOI: 10.1016/S0040-4039(01)82483-7 |
0.513 |
|
| 1974 |
Meyers AI, Kendall PM. Synthesis via oxazolines. VII. Asymmetric reduction of ketones with chiral hydride reagents Tetrahedron Letters. 15: 1337-1340. DOI: 10.1016/S0040-4039(01)82482-5 |
0.558 |
|
| 1974 |
Meyers AI, Knaus G. Synthesis via oxazolines. VI. An asymmetric synthesis of β-hydroxy and β-methoxy alkanoic acids Tetrahedron Letters. 15: 1333-1336. DOI: 10.1016/S0040-4039(01)82481-3 |
0.39 |
|
| 1974 |
Meyers AI, Shaw C. Studies directed toward the total synthesis of maytansine. The preparation and properties of the carbinolamide moiety. Tetrahedron Letters. 15: 717-720. DOI: 10.1016/S0040-4039(01)82313-3 |
0.447 |
|
| 1974 |
Meyers AI, Mihelich ED, Nolen RL. Oxazolines Part 10, Synthesis Of Gamma-Butyrolactones Cheminform. 5. DOI: 10.1002/Chin.197451295 |
0.404 |
|
| 1974 |
NARWID TA, MEYERS AI. ChemInform Abstract: FORMATION OF PYRROLES FROM DIHYDRO-1,3-OXAZINES Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/Chin.197449271 |
0.349 |
|
| 1974 |
Meyers AI, Knaus G, Kamata K. Synthesis Via 2-Oxazolines Part 4, An Asymmetrie Synthesis Of 2-Methylalkanoic Acids From A Chiral Oxazoline Cheminform. 5. DOI: 10.1002/Chin.197412206 |
0.525 |
|
| 1973 |
Meyers AI, Nolen RL, Collington EW, Narwid TA, Strickland RC. A total synthesis of comptothecin and deethyldeoxycamptothecin. The Journal of Organic Chemistry. 38: 1974-82. PMID 4710094 DOI: 10.1021/Jo00951A003 |
0.478 |
|
| 1973 |
Meyers AI, Kovelesky AC, Jurjevich AF. Chemistry of dihydro-1,3-oxazines. XXI. 1,4-Addition of organometallics to 2-alkenyldihydro-1,3-oxazines. Synthesis of .alpha.-substituted aldehydes and ketones Journal of Organic Chemistry. 38: 2136-2143. DOI: 10.1021/Jo00952A005 |
0.433 |
|
| 1973 |
Meyers AI, Nabeya A, Adickes HW, Politzer IR, Malone GR, Kovelesky AC, Nolen RL, Portnoy RC. Synthesis of aldehydes from dihydro-1,3-oxazines Journal of Organic Chemistry. 38: 36-56. DOI: 10.1021/Jo00941A008 |
0.532 |
|
| 1973 |
Hansen JF, Kamata K, Meyers AI. Synthetic studies leading to DE-ring analogs of camptothecin Journal of Heterocyclic Chemistry. 10: 711-714. DOI: 10.1002/Jhet.5570100505 |
0.33 |
|
| 1973 |
MEYERS AI, KOVELESKY AC, JURJEVICH AF. ChemInform Abstract: 1,4-ADDITION OF ORGANOMETALLICS TO 2-ALKENYLDIHYDRO-1,3-OXAZINES, A SYNTHESIS OF ALPHA-SUBSTITUTED ALDEHYDES AND KETONES Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197339186 |
0.437 |
|
| 1973 |
MEYERS AI, NOLEN RL, COLLINGTON EW, NARWID TA, STRICKLAND RC. ChemInform Abstract: EINE TOTALSYNTHESE FUER CAMPTOTHECIN UND DESAETHYL-DESOXYCAMPTOTHECIN Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197336439 |
0.306 |
|
| 1972 |
Meyers AI, Stout DM, Takaya T. Nuclear synthesis of 1,4-dihydropyridines by rearrangement of aziridinobicyclo[2,2,1]pyridazine carboxylates Journal of the Chemical Society, Chemical Communications. 1260-1261. DOI: 10.1039/C39720001260 |
0.471 |
|
| 1972 |
Meyers AI, Strickland RC. Synthesis and properties of 2-(2-cyanoethylidene)-1,3-dithiane and its isomeric ketene thioacetal Journal of Organic Chemistry. 37: 2579-2583. DOI: 10.1021/Jo00981A013 |
0.442 |
|
| 1972 |
Meyers AI, Smith EM. Synthesis of ketones from dihydro-1,3-oxazines via stepwise alkyl or aryl introduction Journal of Organic Chemistry. 37: 4289-4293. DOI: 10.1021/Jo00799A015 |
0.562 |
|
| 1972 |
Meyers AI, Munavu R, Durandetta J. The synthesis of aldehydes from 2-methyl-2-thiazoline Tetrahedron Letters. 13: 3929-3932. DOI: 10.1016/S0040-4039(01)94199-1 |
0.418 |
|
| 1972 |
Haidukewych D, Meyers AI. A mild conversion of carboxylic acids to 2-oxazolines and their utility as a carboxyl masking group against lithium aluminum hydride Tetrahedron Letters. 13: 3031-3034. DOI: 10.1016/S0040-4039(01)85001-2 |
0.357 |
|
| 1971 |
Gault R, Meyers AI. Photocycloaddition of methanol to dihydropyridinium salts Journal of the Chemical Society D: Chemical Communications. 778-779. DOI: 10.1039/C29710000778 |
0.348 |
|
| 1971 |
Meyers AI, Smith EM, Jurjevich AF. Dihydro-1,3-oxazines. XIII. Synthesis of specifically alkylated unsymmetrical ketones. Method for assembling ketones with .alpha.-(quaternary carbons) Journal of the American Chemical Society. 93: 2314-2316. DOI: 10.1021/Ja00738A038 |
0.388 |
|
| 1971 |
Meyers A, Collington E. An efficient total synthesis of propylure, the highly active sex attractant for the pink bollworm moth Tetrahedron. 27: 5979-5985. DOI: 10.1016/S0040-4020(01)91762-4 |
0.384 |
|
| 1971 |
Meyers AI, Narwid TA, Collington EW. Dihydro-1,3-oxazines. XIV . A versatile synthesis of pyrrolo[2,1-c] [1,3,4H] oxazines and a new approach to pyrroles Journal of Heterocyclic Chemistry. 8: 875-876. DOI: 10.1002/Jhet.5570080541 |
0.348 |
|
| 1971 |
Brown RK, Meyers AI, Trefonas LM, Towns RLR, Brown JN. The stereochemical assignments of the four 8-azaestrone configurational isomers Journal of Heterocyclic Chemistry. 8: 279-281. DOI: 10.1002/Jhet.5570080218 |
0.397 |
|
| 1971 |
MEYERS AI, TEMPLE DLJ. ChemInform Abstract: SYNTHESEN UEBER DELTA(2)-OXAZOLINE 3. MITT. DARSTELLUNG VON SUBSTITUIERTEN BENZOESAEUREN UND ESTERN UNTER VERWENDUNG VON GRIGNARD-VERBINDUNGEN AUS 2-BROM-PHENYL-DELTA(2)-OXAZOLINEN Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197103333 |
0.302 |
|
| 1971 |
MEYERS AI, COLLINGTON EW. ChemInform Abstract: SYNTH. UEBER 2-OXAZOLINE 1. MITT. FORMYLIERUNG VON GRIGNARD-REAGENZIEN IN GEGENWART VON HEXAMETHYL-PHOSPHORSAEURETRIAMID Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197103328 |
0.324 |
|
| 1971 |
MEYERS AI, TEMPLE DLJ. ChemInform Abstract: SYNTH. UEBER DELTA(2)-OXAZOLINE 2. MITT. VIELSEITIG ANWENDBARE SYNTH. VON ALIPHATISCHEN CARBONSAEUREN UND ESTERN, MONO- UND DIALKYLIERUNG VON GESCHUETZTEN SAEUREN Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197103300 |
0.31 |
|
| 1970 |
Meyers AI, Singh P. Photoaddition of diphenylacetylene to tetrahydro-2-quinolones Journal of Organic Chemistry. 35: 3022-3030. DOI: 10.1021/Jo00834A036 |
0.336 |
|
| 1970 |
Reine AH, Meyers AI. Azasteroids. IX. Synthesis and stereochemistry of 12-oxo-17-deoxo-8-azaestrone methyl ether Journal of Organic Chemistry. 35: 554-557. DOI: 10.1021/Jo00828A002 |
0.414 |
|
| 1970 |
Meyers AI, Collington EW. Syntheses via-2-oxazolines. I. Formylation of Grignard reagents in the presence of hexamethylphosphoramide Journal of the American Chemical Society. 92: 6676-6678. DOI: 10.1021/Ja00725A069 |
0.48 |
|
| 1970 |
Meyers AI, Temple DL. Syntheses via 2-oxazolines. III. Formation of substituted benzoic acids or esters utilizing the Grignard reagent of 2-(bromophenyl)-2-oxazolines Journal of the American Chemical Society. 92: 6646-6647. DOI: 10.1021/Ja00725A049 |
0.432 |
|
| 1970 |
Meyers AI, Temple DL. Syntheses via 2-oxazolines. II. Versatile synthesis of aliphatic carboxylic acids and esters. Mono-and dialkylation of acids masked by a simple protecting group Journal of the American Chemical Society. 92: 6644-6646. DOI: 10.1021/Ja00725A048 |
0.408 |
|
| 1970 |
Meyers AI, Politzer IR, Bandlish BK, Malone GR. Additions and Corrections - Syntheses via Dihydro-1,3-oxazines. VI. A Carboxyl Protecting Group Stable to the Grigand Reagent. A New Synthesis of Carboxylic Acids. Journal of the American Chemical Society. 92: 1107-1108. DOI: 10.1021/Ja00707A607 |
0.451 |
|
| 1970 |
Meyers AI, Smith EM. Syntheses via dihydro-1,3-oxazines. X. Versatile ketone synthesis involving stepwise alkyl or aryl introduction Journal of the American Chemical Society. 92: 1084-1085. DOI: 10.1021/Ja00707A069 |
0.478 |
|
| 1970 |
Meyers A, Malone G, Adickes H. Syntheses dihydro-1,3-oxazines. XI. A synthesis of functionally substituted aldehydes Tetrahedron Letters. 11: 3715-3718. DOI: 10.1016/S0040-4039(01)98569-7 |
0.496 |
|
| 1970 |
Meyers A, Smith EM. Dihydro-1,3-oxazines. XII. The oxazine α-carbanion-ketenimine rearrangement. Tetrahedron Letters. 11: 4355-4358. DOI: 10.1016/S0040-4039(00)89484-8 |
0.306 |
|
| 1970 |
MEYERS AI, MALONE GR, ADICKES HW. ChemInform Abstract: SYNTHESEN UEBER DIHYDRO-1,3-OXAZINE 11. MITT. SYNTHESE FUNKTIONELL SUBSTITUIERTER ALDEHYDE Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197048297 |
0.483 |
|
| 1970 |
MEYERS AI, SMITH ELIZABETH M. ChemInform Abstract: SYNTH. UEBER DIHYDRO-1,3-OXAZINE 10. MITT. KETONSYNTH. MIT SCHRITTWEISER ALKYL- ODER ARYL-EINFUEHRUNG Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/CHIN.197019249 |
0.378 |
|
| 1969 |
Meyers AI, Kovelesky AC. Syntheses via dihydro-1,3-oxazines. VII. A simple synthesis of unsymmetrical ketones Journal of the American Chemical Society. 91: 5887-5888. DOI: 10.1021/Ja01049A041 |
0.538 |
|
| 1969 |
Meyers AI, Politzer IR, Bandlish BK, Malone GR. Syntheses via dihydro-1,3-oxazines. VI. A carboxyl protecting group stable to the Grignard reagent. A new synthesis of carboxylic acids Journal of the American Chemical Society. 91: 5886-5887. DOI: 10.1021/Ja01049A040 |
0.449 |
|
| 1969 |
Adickes HW, Politzer IR, Meyers AI. Aldehydes from dihydro-1,3-oxazines. IV. Synthesis of .gamma.-hydroxy aldehydes and their .gamma.-oxo derivatives Journal of the American Chemical Society. 91: 2155-2156. DOI: 10.1021/Ja01036A076 |
0.426 |
|
| 1969 |
Meyers AI, Adickes HW, Politzer IR, Beverung WN. Aldehydes from dihydro-1,3-oxazines. III. Synthesis of cycloalkanecarboxaldehydes Journal of the American Chemical Society. 91: 765-767. DOI: 10.1021/Ja01031A055 |
0.481 |
|
| 1969 |
Meyers AI, Nabeya A, Adickes HW, Fitzpatrick JM, Malone GR, Politzer IR. Aldehydes from dihydro-1,3-oxazines. II. Synthesis of .alpha.,.beta.-unsaturated aldehydes and their C-1 deuterated derivatives Journal of the American Chemical Society. 91: 764-765. DOI: 10.1021/Ja01031A054 |
0.354 |
|
| 1969 |
Meyers AI, Nabeya A, Adickes HW, Politzer IR. Aldehydes from dihydro-1,3-oxazines. I. Synthesis of aliphatic aldehydes and their C-1 deuterated derivatives Journal of the American Chemical Society. 91: 763-764. DOI: 10.1021/Ja01031A053 |
0.472 |
|
| 1969 |
Meyers AI, Kovelesky AC. Syntheses with dihydro-1,3-oxazines. IX. A simple synthesis of α-phenylaldehydes and ketones Tetrahedron Letters. 10: 4809-4812. DOI: 10.1016/S0040-4039(01)88816-X |
0.468 |
|
| 1969 |
Meyers AI, Singh S. The chemistry of enaminoketones—V Tetrahedron. 25: 4161-4166. DOI: 10.1016/S0040-4020(01)82951-3 |
0.42 |
|
| 1968 |
Meyers AI, Singh P. Photocycloaddition of diphenylacetylene to a 2-pyridone Chemical Communications (London). 576-577. DOI: 10.1039/C19680000576 |
0.333 |
|
| 1968 |
Singh S, Meyers AI. A simple and versatile heterocyclic synthesis from aminonitriles and ketones Journal of Heterocyclic Chemistry. 5: 737-739. DOI: 10.1002/Jhet.5570050530 |
0.535 |
|
| 1968 |
Meyers AI, Reine AH, Sircar JC, Rao KB, Singh S, and HW, Fitzpatrick M. The chemistry of cyclic enaminoketones. III. Synthesis of bi- and tricyclic enaminoketones from enamine esters and nitriles† Journal of Heterocyclic Chemistry. 5: 151-159. DOI: 10.1002/Jhet.5570050201 |
0.448 |
|
| 1967 |
Meyers AI, Sircar JC. The synthesis of 7-aminobenzo[a]cycloalkano[f]quinolizinium perchlorates. An example of the addition of enamines to the nitrile function. The Journal of Organic Chemistry. 32: 1250-1. PMID 6042156 DOI: 10.1021/Jo01279A097 |
0.324 |
|
| 1967 |
Meyers AI, Singh S. The chemistry of cyclic enaminoketones. II. 1,2-And 1,4-addition of nucleophiles leading to substituted heterocycles Tetrahedron Letters. 8: 5319-5322. DOI: 10.1016/S0040-4039(01)89670-2 |
0.37 |
|
| 1967 |
Meyers AI, Sircar JC. Azasteroids—VI : A facile total synthesis of dl-8-azaestrone methyl ether and related systems Tetrahedron. 23: 785-791. DOI: 10.1016/0040-4020(67)85024-5 |
0.432 |
|
| 1967 |
Meyers AI, Sircar JC, Singh S. A facile cyclization of an enamine nitrile to dihydropyridinium salts Journal of Heterocyclic Chemistry. 4: 461-462. DOI: 10.1002/Jhet.5570040339 |
0.432 |
|
| 1964 |
Meyers AI, Betrus BJ, Ralhan NK, Rao KB. Studies directed toward the total synthesis of novel azasteroids. III. The formation of a hexahydroisoquinoline, octahydroisoquinoline and a decahydro-2h-benzo[a]quinolizine as precursors to 8-azasteroids† Journal of Heterocyclic Chemistry. 1: 13-18. DOI: 10.1002/Jhet.5570010103 |
0.342 |
|
| 1963 |
Meyers AI, Schneller J, Ralhan NK. Studies Directed toward the Total Synthesis of Azasteroids. I. 3,4-Cyclopenteno-5,6-dihydropyridines and 6,6-Tetramethylene-5,6-dihydro-1,3-oxazines1-3 Journal of Organic Chemistry. 28: 2944-2950. DOI: 10.1021/Jo01046A002 |
0.468 |
|
| 1960 |
Meyers AI. Preparation of 5,6-Dihydro-1,3-thiazines and 2-Thiazolines from Mercaptoalcohols and Nitriles1 Journal of Organic Chemistry. 25: 1147-1151. DOI: 10.1021/Jo01077A019 |
0.373 |
|
| 1958 |
MEYERS AI, RITTER JJ. Nitriles in Nuclear Heterocyclic Synthesis. II The Journal of Organic Chemistry. 23: 1918-1922. DOI: 10.1021/Jo01106A026 |
0.623 |
|
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