| Year |
Citation |
Score |
| 2017 |
Stork G, Yamashita A, Hanson RM, Phan L, Phillips E, Dubé D, Bos PH, Clark AJ, Gough M, Greenlee ML, Jiang Y, Jones K, Kitamura M, Leonard J, Liu T, et al. Synthetic Study toward Total Synthesis of (±)-Germine: Synthesis of (±)-4-Methylenegermine. Organic Letters. PMID 28876074 DOI: 10.1021/Acs.Orglett.7B02434 |
0.784 |
|
| 2010 |
STORK G, WEST F, LEE HY, ISAACS RCA, MANABE S. ChemInform Abstract: Total Synthesis of a Natural Cardenolide: (+)-Digitoxigenin (XIV). Cheminform. 28: no-no. DOI: 10.1002/chin.199707213 |
0.381 |
|
| 2009 |
Stork G, Yamashita A, Adams J, Schulte GR, Chesworth R, Miyazaki Y, Farmer JJ. Regiospecific and stereoselective syntheses of (+/-) morphine, codeine, and thebaine via a highly stereocontrolled intramolecular 4 + 2 cycloaddition leading to a phenanthrofuran system. Journal of the American Chemical Society. 131: 11402-6. PMID 19624126 DOI: 10.1021/Ja9038505 |
0.408 |
|
| 2005 |
Stork G, Tang PC, Casey M, Goodman B, Toyota M. Regiospecific and stereoselective syntheses of (+/-)-reserpine and (-)-reserpine. Journal of the American Chemical Society. 127: 16255-62. PMID 16287318 DOI: 10.1002/CHIN.200614205 |
0.781 |
|
| 2003 |
Stork G, Benaim J. Monoalkylation of α,β‐Unsaturated Ketones via Metalloenamines: 1‐Butyl‐10‐methyl‐Δ1(9)‐2‐octalone Organic Syntheses. 69-69. DOI: 10.1002/0471264180.Os057.18 |
0.312 |
|
| 2003 |
Stork G, Dowd SR. Alkylations of Aldehydes via Reaction of the Magnesioenamine Salt of an Aldehyde: 2,2‐Dimethyl‐3‐Phenylpropionaldehyde Organic Syntheses. 46-46. DOI: 10.1002/0471264180.Os054.09 |
0.374 |
|
| 2003 |
Stork G. Heterocycles: Preface Heterocycles. 61: 1. |
0.317 |
|
| 2002 |
Stork G, Niu D, Fujimoto RA, Koft ER, Balkovec JM, Tata JR, Dake GR, Appendino G, Zanardi F, Casiraghi G. The first stereoselective total synthesis of quinine Chemtracts. 15: 175-182. |
0.738 |
|
| 2001 |
Stork G, Niu D, Fujimoto RA, Koft ER, Balkovec JM, Tata JR, Dake GR, Fujimoto A. The first stereoselective total synthesis of quinine. Journal of the American Chemical Society. 123: 3239-42. PMID 11457058 DOI: 10.1021/Ja004325R |
0.75 |
|
| 2001 |
Stork G, Niu D, Fujimoto RA, Koft ER, Balkovec JM, Tata JR, Dake GR. The First Stereoselective Total Synthesis of Quinine [J.Am. Chem. Soc.2001,123(14), 3239−3242]. Journal of the American Chemical Society. 123: 8644-8644. DOI: 10.1021/Ja015138B |
0.71 |
|
| 2000 |
Stork G. [Organic synthesis]. Comptes Rendus De L'AcadéMie Des Sciences. SéRie Iii, Sciences De La Vie. 323: 441-5. PMID 10879291 DOI: 10.1016/S0764-4469(00)00149-9 |
0.337 |
|
| 1999 |
Stork G. Some contributions to regio and stereo control: from Cincholoipon and Cantharidin to the present. Medicinal Research Reviews. 19: 370-87. PMID 10502741 DOI: 10.1002/(Sici)1098-1128(199909)19:5<370::Aid-Med5>3.0.Co;2-8 |
0.44 |
|
| 1998 |
Stork G, Manabe K, Liu L. An Enantioselective Construction of the ABC System of Taxol Journal of the American Chemical Society. 120: 1337-1338. DOI: 10.1021/Ja973559G |
0.308 |
|
| 1996 |
Stork G, West F, Lee HY, Isaacs RCA, Manabe S. The total synthesis of a natural cardenolide: (+)-digitoxigenin Journal of the American Chemical Society. 118: 10660-10661. DOI: 10.1021/Ja962163M |
0.67 |
|
| 1996 |
Stork G, La Clair JJ, Spargo P, Nargund RP, Totah N. Stereocontrolled synthesis of (±)-12a-deoxytetracycline Journal of the American Chemical Society. 118: 5304-5305. DOI: 10.1021/Ja960434N |
0.746 |
|
| 1995 |
Magee TV, Stork G, Fludzinski P. A total synthesis of rac-patchouli alcohol Tetrahedron Letters. 36: 7607-7610. DOI: 10.1016/0040-4039(95)01634-T |
0.352 |
|
| 1994 |
de Groot A, Jansen BJM, Verstegen-Haaksma AA, Swarts HJ, Orru RVA, Stork GA, Wijnberg JBPA. Recent developments in the synthesis of drimane and lactarane sesquiterpenes Pure and Applied Chemistry. 66: 2053-2056. DOI: 10.1351/Pac199466102053 |
0.313 |
|
| 1994 |
Doi T, Robertson J, Stork G, Yamashita A. Regiospecificity in the cyclization of 6-(1-hydroxyalkyl) geraniol derivatives. A simple route to the taxol a-ring system Tetrahedron Letters. 35: 1481-1484. DOI: 10.1016/S0040-4039(00)76737-2 |
0.655 |
|
| 1992 |
Stork G, Hutchinson D, Okabe MO, Parker D, Ra C, Ribéreau F, Suzuki T, Zebovitz T. A total synthesis of calcitriol Pure and Applied Chemistry. 64: 1809-1812. DOI: 10.1351/Pac199264121809 |
0.363 |
|
| 1992 |
Stork G, Franklin P. Multiple Carbon Bond Formation Via the Radical Cyclization of Cycloalkenol Acetals. Application to trans Hydrindan Steroid Precursors Australian Journal of Chemistry. 45: 275-284. DOI: 10.1071/Ch9920275 |
0.306 |
|
| 1992 |
Stork G, Kim G. Stereocontrolled synthesis of disaccharides via the temporary silicon connection Journal of the American Chemical Society. 114: 1087-1088. DOI: 10.1021/Ja00029A047 |
0.38 |
|
| 1991 |
Stork G, Suk Suh H, Kim G. The temporary silicon connection method in the control of regio- and stereochemistry. Applications to radical-mediated reactions. The stereospicific synthesis of C-glycosides Journal of the American Chemical Society. 113: 7054-7056. DOI: 10.1021/Ja00018A063 |
0.355 |
|
| 1991 |
Gijsen HJM, Wijnberg JBPA, Stork GA, de Groot A. The synthesis of (-)-kessane, starting from natural (+)-aromadendrene-II Tetrahedron. 47: 4409-4416. DOI: 10.1016/S0040-4020(01)87109-X |
0.333 |
|
| 1990 |
Stork G, Isaacs RCA. Cine substitution in vinylstannane cross-coupling reactions Journal of the American Chemical Society. 112: 7399-7400. DOI: 10.1021/Ja00176A052 |
0.303 |
|
| 1990 |
Stork G, Zhao K. Total syntheses of (-)-histrionicotoxin and (-)-histrionicotoxin 235A Journal of the American Chemical Society. 112: 5875-5876. DOI: 10.1021/Ja00171A035 |
0.467 |
|
| 1990 |
Stork G, Kobayashi Y, Suzuki T, Zhao K. The allylic epoxide cyclization. A method for the control of regiochemistry and stereochemistry in cyclohexane systems Journal of the American Chemical Society. 112: 1661-1663. DOI: 10.1021/Ja00160A074 |
0.491 |
|
| 1989 |
Stork G. The stereospecific synthesis of reserpine Pure and Applied Chemistry. 61: 439-442. DOI: 10.1351/Pac198961030439 |
0.331 |
|
| 1989 |
Stork G, Keitz PF. An efficient synthesis of alkenyl and alkynyl silyl ethers Tetrahedron Letters. 30: 6981-6984. DOI: 10.1016/S0040-4039(01)93403-3 |
0.441 |
|
| 1989 |
Stork G, Mah R. Introduction of angular methyl groups via radical cyclization Tetrahedron Letters. 30: 3609-3612. DOI: 10.1016/S0040-4039(01)80461-5 |
0.317 |
|
| 1989 |
Stork G, Zhao K. A stereoselective synthesis of (Z)-1-iodo-1-alkenes Tetrahedron Letters. 30: 2173-2174. DOI: 10.1016/S0040-4039(00)99640-0 |
0.603 |
|
| 1989 |
Stork G, Zhao K. A simple method of dethioacetalization Tetrahedron Letters. 30: 287-290. DOI: 10.1016/S0040-4039(00)95181-5 |
0.492 |
|
| 1989 |
Stork G, Kahne D. Efficient Regio- and Stereocontrolled Synthesis of Highly Functionalized Polycyclic Systems Using the Diels-Alder Addition of Stannyl-Substituted Vinylketeneacetals Israel Journal of Chemistry. 29: 243-246. DOI: 10.1002/Ijch.198900033 |
0.626 |
|
| 1988 |
Stork G. Radical Cyclization in the Control of Regio- and Stereochemistry Bulletin of the Chemical Society of Japan. 61: 149-154. DOI: 10.1246/Bcsj.61.149 |
0.328 |
|
| 1988 |
Stork G, Polt RL, Li Y, Houk KN. Theoretical studies of the lithiation of enamines Journal of the American Chemical Society. 110: 8360-8367. DOI: 10.1021/Ja00233A013 |
0.544 |
|
| 1988 |
Stork G, Reynolds ME. Allylic radicals in cyclization reactions Journal of the American Chemical Society. 110: 6911-6913. DOI: 10.1021/Ja00228A065 |
0.321 |
|
| 1987 |
Stork G, Rychnovsky SD. Iterative butenolide construction of polypropionate chains: Application to an efficient synthesis of (+)(9S)-dihydroerythronolide A Pure and Applied Chemistry. 59: 345-352. DOI: 10.1351/Pac198759030345 |
0.572 |
|
| 1987 |
Stork G, Rychnovsky SD. Concise total synthesis of (+)-(9S)-dihydroerythronolide A Journal of the American Chemical Society. 109: 1565-1567. DOI: 10.1021/Ja00239A045 |
0.616 |
|
| 1987 |
Stork G, Rychnovsky SD. Iterative butenolide construction of polypropionate chains Journal of the American Chemical Society. 109: 1564-1565. DOI: 10.1021/Ja00239A044 |
0.468 |
|
| 1987 |
Stork G, Saccomano NA. Enantioselective synthesis of an intermediate for the intramolecular Diels-Alder construction of 11-ketosteroids Tetrahedron Letters. 28: 2087-2090. DOI: 10.1016/S0040-4039(00)96050-7 |
0.756 |
|
| 1987 |
Stork G, Krafft ME, Biller SA. An approach to gelsemine Tetrahedron Letters. 28: 1035-1038. DOI: 10.1016/S0040-4039(00)95904-5 |
0.601 |
|
| 1987 |
STORK G, SACCOMANO NA. ChemInform Abstract: Chiral Induction in the Construction of Vicinally Substituted Cyclopentanones via the Intramolecular Conjugate Addition of Chiral β-Keto Esters. Cheminform. 18. DOI: 10.1002/chin.198734166 |
0.741 |
|
| 1986 |
Stork G, Sher PM, Chen HL. Radical cyclization-trapping in the synthesis of natural products. A simple, stereocontrolled route to prostaglandin F2α Journal of the American Chemical Society. 108: 6384-6385. DOI: 10.1021/Ja00280A043 |
0.402 |
|
| 1986 |
Stork G, Shiner CS, Cheng CW, Polt RL. Deprotonation of chelating enamines. Direct formation of β-lithio enamines Journal of the American Chemical Society. 108: 304-305. DOI: 10.1021/Ja00262A025 |
0.544 |
|
| 1986 |
Stork G, Shiner CS, Cheng CW, Polt RL. Deprotonation of chelating enamines. Direct formation of .beta.-lithio enamines Journal of the American Chemical Society. 108: 304-305. DOI: 10.1021/ja00262a025 |
0.507 |
|
| 1986 |
Stork G, Sher PM. A catalytic tin system for trapping of radicals from cyclization reactions. Regio- and stereocontrolled formation of two adjacent chiral centers Journal of the American Chemical Society. 108: 303-304. DOI: 10.1021/Ja00262A024 |
0.351 |
|
| 1986 |
Stork G, Mook R. Five vs six membered ring formation in the vinyl radical cyclization Tetrahedron Letters. 27: 4529-4532. DOI: 10.1016/S0040-4039(00)84995-3 |
0.329 |
|
| 1986 |
STORK G, SHER PM. ChemInform Abstract: A Catalytic Tin System for Trapping of Radicals from Cyclization Reactions. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198620073 |
0.318 |
|
| 1985 |
Stork G, Baine NH. Vinyl radical cyclization in the synthesis of natural products: seychellene Tetrahedron Letters. 26: 5927-5930. DOI: 10.1016/S0040-4039(00)98263-7 |
0.396 |
|
| 1985 |
Stork G, Kahn M. Control of ring junction stereochemistry via radical cyclization Journal of the American Chemical Society. 107: 500-501. DOI: 10.1002/Chin.198521087 |
0.319 |
|
| 1984 |
Stork G, Clark G, Weller T. Simple preparation of a useful C/D-ring fragment for the construction of 11-keto steroids Tetrahedron Letters. 25: 5367-5370. DOI: 10.1016/S0040-4039(01)91285-7 |
0.399 |
|
| 1984 |
Polt RL, Stork G, Carpenter GB, Williard PG. X-ray crystal structure of N-(2-lithiocyclohexenyl)-N,N′,N′-trimethyl-1,3-propanediamine: A pentavalent lithium? Journal of the American Chemical Society. 106: 4276-4277. DOI: 10.1002/Chin.198445057 |
0.641 |
|
| 1983 |
Stork G, Nakamura E. A simplified total synthesis of cytochalasins via an intramolecular Diels-Alder reaction Journal of the American Chemical Society. 105: 5510-5512. DOI: 10.1021/Ja00354A072 |
0.433 |
|
| 1983 |
Stork G, Mook R, Biller SA, Rychnovsky SD. Free-radical cyclization of bromoacetals. Use in the construction of bicyclic acetals and lactones Journal of the American Chemical Society. 105: 3741-3742. DOI: 10.1021/Ja00349A082 |
0.524 |
|
| 1983 |
Stork G, Mook R. Vinyl radical cyclization. 2. Dicyclization via selective formation of unsaturated vinyl radicals by intramolecular addition to triple bonds. Applications to the synthesis of butenolides and furans Journal of the American Chemical Society. 105: 3720-3722. DOI: 10.1021/Ja00349A067 |
0.371 |
|
| 1983 |
Stork G, Poirier JM. 2-Substituted tetrahydrofurans of known absolute stereochemistry by SCN′ chirality transfer Journal of the American Chemical Society. 105: 1073-1074. DOI: 10.1021/Ja00342A081 |
0.326 |
|
| 1983 |
Stork G, Kahne DE. Stereocontrol in homogeneous catalytic hydrogenation via hydroxyl group coordination Journal of the American Chemical Society. 105: 1072-1073. DOI: 10.1021/Ja00342A080 |
0.493 |
|
| 1983 |
Stork G, Stryker JM. Highly stereoselective axial addition of ethynyl carbanions to the carbonyl of cyclohexenones Tetrahedron Letters. 24: 4887-4890. DOI: 10.1016/S0040-4039(01)99802-8 |
0.577 |
|
| 1983 |
Stork G, Atwal KS. Acid catalyzed intramolecular conjugate addition as a route to trans hydrindane systems Tetrahedron Letters. 24: 3819-3822. DOI: 10.1016/S0040-4039(00)94283-7 |
0.451 |
|
| 1983 |
Stork G, Kahn M. A highly stereoselective osmium tetroxide-catalyzed hydroxylation of γ-hydroxy α,β-usaturated esters Tetrahedron Letters. 24: 3951-3954. DOI: 10.1016/S0040-4039(00)88233-7 |
0.324 |
|
| 1983 |
Ficini J, Guingant A, J'Angelo J, Stork G. Synthese stereoselective des barcis et bartrans carboxy-4 Tetrahedron Letters. 24: 907-910. DOI: 10.1016/S0040-4039(00)81561-0 |
0.698 |
|
| 1983 |
Stork G, Winkler JD, Saccomano NA. Stereochemical control in the construction of vicinally substituted cyclopentanes and cyclohexanes. Intramolecular conjugate addition of β-ketoester anions. Tetrahedron Letters. 24: 465-468. DOI: 10.1016/S0040-4039(00)81438-0 |
0.779 |
|
| 1983 |
FICINI J, GUINGANT A, D'ANGELO J, STORK G. ChemInform Abstract: STEREOSELECTIVE SYNTHESIS OF CIS- AND TRANS-4-CARBOXY-3A,4,5,6-TETRAHYDROINDAN-1-ONES Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198324194 |
0.72 |
|
| 1982 |
Stork G, Paterson I, Lee FKC. Stereoselective synthesis of the chiral sequence of erythronolide A Journal of the American Chemical Society. 104: 4686-4688. DOI: 10.1021/Ja00381A035 |
0.55 |
|
| 1982 |
Stork G, Winkler JD, Shiner CS. Stereochemical control of intramolecular conjugate addition. A short, highly stereoselective synthesis of adrenosterone Journal of the American Chemical Society. 104: 3767-3768. DOI: 10.1021/Ja00377A058 |
0.638 |
|
| 1982 |
Stork G, Sherman DH. Efficient de novo construction of the indanpropionic acid precursor of 11-keto steroids. An improved internal Diels-Alder sequence Journal of the American Chemical Society. 104: 3758-3759. DOI: 10.1021/Ja00377A052 |
0.494 |
|
| 1982 |
Stork G, Baine NH. Cyclization of vinyl radicals: A new versatile method for the construction of five- and six-membered rings Journal of the American Chemical Society. 104: 2321-2323. DOI: 10.1021/Ja00372A042 |
0.334 |
|
| 1982 |
Stork G, Shiner CS, Winkler JD. Stereochemical control of the internal Michael reaction. A new construction of trans-hydrindane systems Journal of the American Chemical Society. 104: 310-312. DOI: 10.1021/Ja00365A067 |
0.528 |
|
| 1982 |
Stork G, Atwal KS. An isomerization-claisen rearrangement route to olefinic dicarbonyl starting materials for conjugate cyclization Tetrahedron Letters. 23: 2073-2076. DOI: 10.1016/S0040-4039(00)87264-0 |
0.394 |
|
| 1980 |
Stork G, Logusch EW. Reductive alkylation of enediones. 2. Synthesis of corticosteroids [44] Journal of the American Chemical Society. 102: 1219-1220. DOI: 10.1021/Ja00523A079 |
0.505 |
|
| 1980 |
Stork G, Logusch EW. Reductive alkylation of enediones. 1 Journal of the American Chemical Society. 102: 1218-1219. DOI: 10.1021/Ja00523A078 |
0.352 |
|
| 1980 |
Stork G, Nair V. Additions and Corrections - A Stereocontrolled Synthesis of the (±) Djerassi-Prelog Lactonic Acid Journal of the American Chemical Society. 102: 891-891. DOI: 10.1021/Ja00522A604 |
0.361 |
|
| 1980 |
Stork G, Clark Still W, Singh J, Takei S. Elaboration of a tricyclic gibberellic acid intermediate Tetrahedron Letters. 21: 4051-4054. DOI: 10.1016/0040-4039(80)88063-4 |
0.445 |
|
| 1980 |
Stork G, Logusch EW. Reductive alkylation of enediones. 2. Synthesis of corticosteroids Cheminform. 11. DOI: 10.1002/Chin.198019135 |
0.505 |
|
| 1980 |
Stork G, Singh J. An Unusually Simple Construction Of Ring A Of Gibberellic Acid Cheminform. 11. DOI: 10.1002/Chin.198007357 |
0.315 |
|
| 1980 |
Stork G, Morgans DJJ. A simple, stereospecific synthesis of the skeleton of the lycorine alkaloids Cheminform. 11. DOI: 10.1002/Chin.198007340 |
0.319 |
|
| 1979 |
Stork G, Nakamura E. Large-ring lactones by internal ketophosphonate cyclizations Journal of Organic Chemistry. 44: 4010-4011. DOI: 10.1021/Jo01336A068 |
0.342 |
|
| 1979 |
Stork G, Morgans DJ. A simple, stereospecific synthesis of the skeleton of the lycorine alkaloids [28] Journal of the American Chemical Society. 101: 7110-7111. DOI: 10.1021/Ja00517A075 |
0.504 |
|
| 1979 |
Stork G, Singh J. An unusually simple construction of ring A of gibberellic acid Journal of the American Chemical Society. 101: 7109-7110. DOI: 10.1021/Ja00517A074 |
0.315 |
|
| 1979 |
Stork G, Boeckmann RK, Taber DF, Clark Still W, Singh J. Reductive cyclization of ethynyl ketones in the construction of a significant tricyclic intermediate for the synthesis of gibberellic acid [26] Journal of the American Chemical Society. 101: 7107-7109. DOI: 10.1021/Ja00517A073 |
0.626 |
|
| 1979 |
Stork G, Schoofs AR. Concerted intramolecular displacement with rearrangement in allylic systems. Displacement of an allylic ester with a carbanion [16] Journal of the American Chemical Society. 101: 5081-5082. DOI: 10.1021/Ja00511A057 |
0.342 |
|
| 1979 |
Stork G, Nair V. A stereocontrolled synthesis of the (.+-.) Djerassi-Prelog lactonic acid Journal of the American Chemical Society. 101: 1315-1316. DOI: 10.1021/Ja00499A061 |
0.414 |
|
| 1979 |
Stork G, Logusch EW. organocuprate reactions of enone lactones. I. Synthesis of trans-fused rings via conjugate addition Tetrahedron Letters. 20: 3361-3364. DOI: 10.1016/S0040-4039(01)95409-7 |
0.426 |
|
| 1979 |
Stork G, Still WC, Singh J. Unusual regiospecificity in the enolization of a ketone as the result of differences in energy to achieve the best overlap of an alpha hydrogen Tetrahedron Letters. 20: 5077-5078. DOI: 10.1016/S0040-4039(01)86794-0 |
0.505 |
|
| 1979 |
Bernstein PR, Stork G. Routes to bicyclo [X.3.0] ring systems: stereoselective syntheses of cis and trans-8-methylhydrindans Tetrahedron Letters. 20: 1967-1970. DOI: 10.1016/S0040-4039(01)86239-0 |
0.363 |
|
| 1979 |
Morgans DJ, Stork G. An intramolecular diels-alder approach to the galanthan ring system Tetrahedron Letters. 20: 1959-1962. DOI: 10.1016/S0040-4039(01)86237-7 |
0.367 |
|
| 1978 |
Stork G, Nakahara Y, Nakahara Y, Greenlee WJ. Total synthesis of cytochalasin B Journal of the American Chemical Society. 100: 7775-7777. DOI: 10.1021/Ja00492A082 |
0.363 |
|
| 1978 |
Stork G, Taber DF, Marx M. The intramolecular Michael addition as a route to angularly substituted cis-hydrindanes Tetrahedron Letters. 19: 2445-2448. DOI: 10.1016/S0040-4039(01)94796-3 |
0.55 |
|
| 1978 |
STORK G, WILLIARD PG. ChemInform Abstract: FIVE- AND SIX-MEMBERED-RING FORMATION FROM OLEFINIC α,β-EPOXY KETONES AND HYDRAZINE Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197803151 |
0.524 |
|
| 1977 |
Stork G, Takahashi T. Chiral synthesis of prostaglandins (PGE1) from D-glyceraldehyde. Journal of the American Chemical Society. 99: 1275-6. PMID 833403 DOI: 10.1002/Chin.197719371 |
0.38 |
|
| 1977 |
Stork G, Williard PG. Five- and six-membered-ring formation from olefinic .alpha.,.beta.-epoxy ketones and hydrazine Journal of the American Chemical Society. 99: 7067-7068. DOI: 10.1021/Ja00463A053 |
0.54 |
|
| 1977 |
Stork G, Williard PG. Five- and six-membered-ring formation from olefinic α,β-epoxy ketones and hydrazine [7] Journal of the American Chemical Society. 99: 7067-7068. |
0.516 |
|
| 1976 |
Stork G, Raucher S. Letter: Chiral synthesis of prostaglandins from carbohydrates. Synthesis of (+)-15-(S)-prostaglandin A2. Journal of the American Chemical Society. 98: 1583-4. PMID 1249367 DOI: 10.1021/Ja00422A053 |
0.74 |
|
| 1976 |
Stork G, Leong AY, Touzin AM. Alkylation and Michael additions of glycine ethyl ester. Use in alpha-amino acid synthesis and as acyl carbanion equivalent. The Journal of Organic Chemistry. 41: 3491-3. PMID 978298 DOI: 10.1021/Jo00883A044 |
0.379 |
|
| 1976 |
Stork G, Kraus G. The Ene reaction as a route to 3-hydroxycyclopentanone derivatives. Application to the prostaglandins. Journal of the American Chemical Society. 98: 6747-8. PMID 972230 DOI: 10.1021/JA00437A080 |
0.516 |
|
| 1976 |
Stork G, MacDonald T. Additions and Corrections - A Synthesis of d,l-Muscone from Cyclododecanone Journal of the American Chemical Society. 98: 2370-2370. DOI: 10.1021/Ja00424A600 |
0.308 |
|
| 1976 |
Stork G, Kraus GA. A new synthesis of vinylogous aldols and polyenones Journal of the American Chemical Society. 98: 2351-2352. DOI: 10.1002/Chin.197627180 |
0.6 |
|
| 1976 |
Stork G, Raucher S. Chiral Synthesis Of Prostaglandins From Carbohydrates. Synthesis Of (+)-15-(S)-Prostaglandin A2 Cheminform. 7. DOI: 10.1002/Chin.197623335 |
0.43 |
|
| 1976 |
Stork G, Kraus GA. A new synthesis of vinylogous aldols and polyenones [11] Journal of American Chemical Society. 98: 2351-2352. |
0.345 |
|
| 1975 |
Stork G, Isobe M. Letter: A simple total synthesis of prostaglandins from 4-cumyloxy-2-cyclopentenone. Journal of the American Chemical Society. 97: 6260-1. PMID 1176736 DOI: 10.1021/Ja00854A061 |
0.483 |
|
| 1975 |
Stork G, Isobe M. Letter: A general approach to prostaglandins via methylenecyclopentanones. Total synthesis of (+/- prostaglandin F2 alpha. Journal of the American Chemical Society. 97: 4745-6. PMID 1159227 DOI: 10.1021/Ja00849A042 |
0.3 |
|
| 1975 |
Stork G, Kowalski C, Garcia G. Letter: A route to prostaglandins via a general synthesis of 4-hydroxycyclopentenones. Journal of the American Chemical Society. 97: 3258-60. PMID 1133349 DOI: 10.1021/Ja00844A078 |
0.452 |
|
| 1975 |
Stork G. The use of kinetically generated unstable enolate ions in the regiospecific formation of carbonxarbon bonds. Specific applications to annelation processes Pure and Applied Chemistry. 43: 553-562. DOI: 10.1351/Pac197543030553 |
0.318 |
|
| 1975 |
Stork G, MacDonald TL. Synthesis of d,l-muscone from cyclododecanone Journal of the American Chemical Society. 97: 1264-1265. DOI: 10.1021/Ja00838A062 |
0.302 |
|
| 1975 |
Stork G, Depezay JC, d'Angelo J. Synthesis of small rings the protected cyanohydrin method. Tetrahedron Letters. 16: 389-392. DOI: 10.1016/S0040-4039(00)71874-0 |
0.41 |
|
| 1975 |
Stork G, Kowalski C, Garcia G. A Route To Prostaglandins Via A General Synthesis Of 4-Hydroxycyclopentenones Cheminform. 6. DOI: 10.1002/Chin.197533406 |
0.455 |
|
| 1974 |
Stork G, Cohen JF. Ring size in epoxynitrile cyclization. General synthesis of functionally substituted cyclobutanes. Application to (+-)-grandisol Journal of the American Chemical Society. 96: 5270-5272. DOI: 10.1021/Ja00823A053 |
0.422 |
|
| 1974 |
Stork G, Cama LD, Coulson DR. Epoxynitrile cyclization. General method of ring formation Journal of the American Chemical Society. 96: 5268-5270. DOI: 10.1021/Ja00823A052 |
0.324 |
|
| 1974 |
Stork G, Jung ME, Colvin E, Noel Y. Synthetic routes to halomethyl vinylsilanes Journal of the American Chemical Society. 96: 3684-3686. DOI: 10.1021/Ja00818A071 |
0.508 |
|
| 1974 |
Stork G, Jung ME. Vinylsilanes as carbonyl precursors. Use in annelation reactions Journal of the American Chemical Society. 96: 3682-3684. DOI: 10.1021/Ja00818A070 |
0.468 |
|
| 1974 |
Stork G, Kraus GA, Garcia GA. Regiospecific aldol condensations of the kinetic lithium enolates of methyl ketones The Journal of Organic Chemistry. 39: 3459-3460. DOI: 10.1002/Chin.197511195 |
0.519 |
|
| 1974 |
STORK G, CAMA LD, COULSON DR. ChemInform Abstract: EPOXYNITRILE CYCLIZATION, A GENERAL METHOD FOR RING FORMATION Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/Chin.197442137 |
0.345 |
|
| 1973 |
Stork G, Danheiser RL. Regiospecific alkylation of cyclic .beta.-diketone enol ethers. General synthesis of 4-alkylcyclohexenones The Journal of Organic Chemistry. 38: 1775-1776. DOI: 10.1021/Jo00949A048 |
0.37 |
|
| 1973 |
Stork G, Ganem B. .alpha.-Silylated vinyl ketones. New class of reagents for the annelation of ketones Journal of the American Chemical Society. 95: 6152-6153. DOI: 10.1021/Ja00799A072 |
0.519 |
|
| 1973 |
Stork G, Danheiser RL, Ganem B. Spiroannelation of enol ethers of cyclic 1,3-diketones. Simple stereospecific synthesis of .beta.-vetivone Journal of the American Chemical Society. 95: 3414-3415. DOI: 10.1021/Ja00791A074 |
0.562 |
|
| 1973 |
Stork G, Gardner JO, Beckman RK, Parker KA. Haloketal cyclization. General method for the synthesis of functionalized cis bicyclic ketones Journal of the American Chemical Society. 95: 2014-2016. DOI: 10.1021/Ja00787A052 |
0.594 |
|
| 1973 |
STORK G, GARDNER JO, BOECKMAN RKJ, PARKER KA. ChemInform Abstract: CYCLISIERUNG VON HALOGENKETALEN, ALLGEMEINE METHODE ZUR SYNTH. VON FUNKTIONALISIERTEN CIS-BICYCLISCHEN KETONEN Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197322156 |
0.495 |
|
| 1972 |
Stork G, Tabak JM, Blount JF. Total synthesis of (+-)-byssochlamic acid Journal of the American Chemical Society. 94: 4735-4737. DOI: 10.1021/Ja00768A055 |
0.404 |
|
| 1972 |
Stork G, Guthikonda RN. A general synthesis of esters of acryloyl acetic acid and their homologs. Tetrahedron Letters. 13: 2755-2758. DOI: 10.1016/S0040-4039(01)84925-X |
0.403 |
|
| 1971 |
Stork G, Schultz AG. The total synthesis of dl-camptothecin. Journal of the American Chemical Society. 93: 4074-5. PMID 5138309 DOI: 10.1021/Ja00745A056 |
0.817 |
|
| 1971 |
Stork G, Ohashi M, Kamachi H, Kakisawa H. Pyridine synthesis via 4-(3-oxoalkyl)isoxazoles The Journal of Organic Chemistry. 36: 2784-2786. DOI: 10.1021/Jo00818A013 |
0.515 |
|
| 1971 |
Stork G, Maldonado L. Anions of protected cyanohydrins as acyl carbanion equivalents and their use in a new synthesis of ketones Journal of the American Chemical Society. 93: 5286-5287. DOI: 10.1021/Ja00749A069 |
0.443 |
|
| 1971 |
Stork G, Uyeo S, Wakamatsu T, Grieco P, Labovitz J. Total synthesis of lupeol Journal of the American Chemical Society. 93: 4945-4947. DOI: 10.1021/Ja00748A068 |
0.497 |
|
| 1971 |
Stork G, Nelson GL, Rouessac F, Gringore O. Versatile synthesis of cyclopentenones Journal of the American Chemical Society. 93: 3091-3092. DOI: 10.1021/Ja00741A070 |
0.508 |
|
| 1971 |
Stork G, Colvin E. New synthesis of aldehydes via vinylsilanes Journal of the American Chemical Society. 93: 2080-2081. DOI: 10.1021/Ja00737A057 |
0.456 |
|
| 1971 |
Stork G, A. Grieco P. Olefin participation in the acid-catalyzed opening of acylcyclopropanes. IV. Cyclization of 5-methyl-6--(-3-pentenyl)bicyclo(3.1.0)hexan-2-one. Tetrahedron Letters. 12: 1807-1810. DOI: 10.1016/S0040-4039(01)87467-0 |
0.331 |
|
| 1971 |
STORK G, OHASHI M, KAMACHI H, KAKISAWA H. ChemInform Abstract: EINE NEUE PYRIDIN-SYNTH. UEBER 4-(3-OXALKYL)-ISOXAZOLE Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197152320 |
0.328 |
|
| 1971 |
STORK G, SCHULTZ AG. ChemInform Abstract: TOTALSYNTH. VON DL-CAMPTOTHECIN Chemischer Informationsdienst. Organische Chemie. 2. DOI: 10.1002/Chin.197144389 |
0.651 |
|
| 1969 |
Stork G, Stotter PL. A New Approach to the Stereospecific Synthesis of Angularly Substituted Polycyclic Systems Journal of the American Chemical Society. 91: 7780-7781. DOI: 10.1021/Ja50001A065 |
0.385 |
|
| 1969 |
Stork G, Gregson M. Aryl participation in concerted cyclization of cyclopropyl ketones Journal of the American Chemical Society. 91: 2373-2374. DOI: 10.1021/Ja01037A032 |
0.356 |
|
| 1969 |
Stork G, Grieco PA, Gregson M. Synthesis of allylic halides and 1,5-dienes from allylic alcohols Tetrahedron Letters. 10: 1393-1395. DOI: 10.1016/S0040-4039(01)87896-5 |
0.341 |
|
| 1969 |
Stork G, Gregson M, Grieco PA. A convenient route to and trisubstituted olefins from geraniol and nerol Tetrahedron Letters. 10: 1391-1392. DOI: 10.1016/S0040-4039(01)87895-3 |
0.377 |
|
| 1968 |
Stork G, Kretchmer RA, Schlessinger RH. The stereospecific total synthesis of dl-lycopodine. Journal of the American Chemical Society. 90: 1647-8. PMID 5636803 DOI: 10.1021/Ja01008A042 |
0.775 |
|
| 1968 |
Stork G. Progress in the synthesis of polycyclic natural products: The total synthesis of lycopodine Pure and Applied Chemistry. 17: 383-402. DOI: 10.1351/Pac196817030383 |
0.447 |
|
| 1967 |
Stork G, McMurry JE. Stereospecific total synthesis of steroids via isoxazole annelation. dl-D-Homotestosterone and dl-progesterone Journal of the American Chemical Society. 89: 5464-5465. DOI: 10.1021/Ja00997A035 |
0.367 |
|
| 1967 |
Stork G, McMurry JE. General synthesis of 4-isoxazolecarboxylic acids Journal of the American Chemical Society. 89: 5461-5462. DOI: 10.1021/Ja00997A033 |
0.389 |
|
| 1967 |
Stork G, Danishefsky S, Ohashi M. Isoxazole annelation reaction. Method for the construction of cyclohexenone rings in polycyclic systems Journal of the American Chemical Society. 89: 5459-5460. DOI: 10.1021/Ja00997A031 |
0.474 |
|
| 1965 |
STORK G, CHEUNG HT. TOTAL SYNTHESIS OF THE CEPHALOSPORIN ANTIBIOTICS. I. THE DIHYDROTHIAZINE SYSTEM OF CEPHALOSPORIN CC. Journal of the American Chemical Society. 87: 3783-4. PMID 14338117 DOI: 10.1021/Ja01094A052 |
0.407 |
|
| 1965 |
Stork G, Malhotra S, Thompson H, Uchibayashi M. A New Cyclization. 2-Methylenecyclopentanols by the Chemical Reduction of γ-Ethinyl Ketones Journal of the American Chemical Society. 87: 1148-1149. DOI: 10.1021/Ja01083A048 |
0.342 |
|
| 1965 |
Stork G, Rosen P, Goldman N, Coombs RV, Tsuji J. Alkylation and Carbonation of Ketones by Trapping the Enolates from the Reduction of α,β-Unsaturated Ketones Journal of the American Chemical Society. 87: 275-286. DOI: 10.1021/Ja01080A025 |
0.511 |
|
| 1964 |
Stork G. Progress in the synthesis of polycyclic natural products Pure and Applied Chemistry. 9: 131-144. DOI: 10.1351/Pac196409010131 |
0.375 |
|
| 1964 |
Stork G, Borch R. A Synthesis ofcis-Jasmone Journal of the American Chemical Society. 86: 936-937. DOI: 10.1021/Ja01059A047 |
0.708 |
|
| 1964 |
Stork G, Borch R. A New Synthesis of 1,4- and 1,5-Diketones Journal of the American Chemical Society. 86: 935-936. DOI: 10.1021/Ja01059A046 |
0.669 |
|
| 1964 |
Stork G, Tomasz M. A New Synthesis of Cyclohexenones: The Double Michael Addition of Vinyl Ethynyl Ketones to Active Methylene Compounds. Application to the Total Synthesis ofdl-Griseofulvin Journal of the American Chemical Society. 86: 471-478. DOI: 10.1021/Ja01057A038 |
0.682 |
|
| 1964 |
Djerassi C, Burakevich J, Chamberlin JW, Elad D, Toda T, Stork G. Optical Rotatory Dispersion Studies. XCII.1Some Observations on the Conformation ofcis-10-Methyl-2-decalones2 Journal of the American Chemical Society. 86: 465-471. DOI: 10.1021/Ja01057A037 |
0.345 |
|
| 1963 |
Stork G, Dolfini JE. The Total Synthesis ofdl-Aspidospermine and ofdl-Quebrachamine Journal of the American Chemical Society. 85: 2872-2873. DOI: 10.1021/Ja00901A061 |
0.496 |
|
| 1963 |
Stork G, Dowd SR. A New Method for the Alkylation of Ketones and Aldehydes: the C-Alkylation of the Magnesium Salts of N-Substituted Imines Journal of the American Chemical Society. 85: 2178-2180. DOI: 10.1021/Ja00897A040 |
0.358 |
|
| 1962 |
Stork G, Darling SD, Harrison IT, Wharton PS. A Stereospecific Total Synthesis of 18-Substituted Steroids. Application to the Synthesis ofdl-Conessine Journal of the American Chemical Society. 84: 2018-2020. DOI: 10.1021/Ja00869A060 |
0.504 |
|
| 1962 |
Stork G, Borowitz IJ. Four-Membered Sulfones From Enamines and Aliphatic Sulfonyl Halides Journal of the American Chemical Society. 84: 313-313. DOI: 10.1021/Ja00861A042 |
0.32 |
|
| 1962 |
Stork G, Tomasz M. A Stereospecific Total Synthesis of Griseofulvin Journal of the American Chemical Society. 84: 310-312. DOI: 10.1021/Ja00861A040 |
0.706 |
|
| 1961 |
Stork G, Ficini J. INTRAMOLECULAR CYCLIZATION OF UNSATURATED DIAZOKETONES Journal of the American Chemical Society. 83: 4678-4678. DOI: 10.1021/Ja01483A055 |
0.769 |
|
| 1961 |
Stork G, Clarke FH. Cedrol: Stereochemistry and Total Synthesis Journal of the American Chemical Society. 83: 3114-3125. DOI: 10.1021/Ja01475A030 |
0.508 |
|
| 1961 |
Stork G, Rosen P, Goldman NL. THE α-ALKYLATION OF ENOLATES FROM THE LITHIUM-AMMONIA REDUCTION OF α,β-UNSATURATED KETONES Journal of the American Chemical Society. 83: 2965-2966. DOI: 10.1021/Ja01474A051 |
0.306 |
|
| 1961 |
Stork G, Tsuji J. LITHIUM-AMMONIA REDUCTION OF α,β-UNSATURATED KETONES. II. FORMATION AND ALKYLATION OF A β-CARBANION INTERMEDIATE Journal of the American Chemical Society. 83: 2783-2784. DOI: 10.1021/Ja01473A053 |
0.499 |
|
| 1960 |
Stork G, Worrall WS, Pappas JJ. Synthesis and Reactions of Glycidonitriles. Transformation into α-Haloacyl Compounds and Aminoalcohols Journal of the American Chemical Society. 82: 4315-4323. DOI: 10.1021/Ja01501A048 |
0.385 |
|
| 1960 |
Stork G, Borowitz IJ. The Synthesis of Substituted 1-Methylcyclohexanecarboxylic Acids and the Stereochemistry of the Favorski[UNK]i Rearrangement Journal of the American Chemical Society. 82: 4307-4315. DOI: 10.1021/Ja01501A047 |
0.447 |
|
| 1960 |
Stork G, Darling SD. STEREOCHEMISTRY OF THE LITHIUM-AMMONIA REDUCTION OF α,β-UNSATURATED KETONES Journal of the American Chemical Society. 82: 1512-1513. DOI: 10.1021/Ja01491A068 |
0.308 |
|
| 1960 |
Stork G, Bersohn M. A STEREOSPECIFIC REACTION OF CARBON MONOXIDE Journal of the American Chemical Society. 82: 1261-1262. DOI: 10.1021/Ja01490A068 |
0.585 |
|
| 1959 |
Stork G, Davies JE, Meisels A. THE TOTAL SYNTHESIS OF A NATURALLY OCCURRING PENTACYCLIC TRITERPENE SYSTEM Journal of the American Chemical Society. 81: 5516-5517. DOI: 10.1021/Ja01529A074 |
0.684 |
|
| 1958 |
Stork G, Khastgir HN, Solo AJ. SYNTHESIS OF 17,18-BISNORSTEROIDS Journal of the American Chemical Society. 80: 6457-6458. DOI: 10.1021/Ja01556A076 |
0.823 |
|
| 1957 |
Stork G, Hill RK. The Stereospecific Synthesis of dl-Alloyohimbane and dl-3-Epialloyohimbane1 Journal of the American Chemical Society. 79: 495-500. DOI: 10.1021/Ja01632A114 |
0.64 |
|
| 1957 |
Stadler PA, Eschenmoser A, Schinz H, Stork G. Untersuchungen über den sterischen Verlauf säurekatalysierter Cyclisationen bei terpenoiden Polyenverbindungen. 3. Mitteilung. Zur Stereochemie der Bicyclofarnesylsäuren Helvetica Chimica Acta. 40: 2191-2198. DOI: 10.1002/hlca.19570400719 |
0.35 |
|
| 1956 |
Stork G, White WN. The Stereochemistry of the SN2' Reaction. I. Preparation of Pure trans-6-Alkyl-2-cyclohexen-1-ols Journal of the American Chemical Society. 78: 4604-4608. DOI: 10.1021/Ja01599A024 |
0.373 |
|
| 1956 |
Stork G, Loewenthal HJE, Mukharji PC. A TOTAL SYNTHESIS OF 1-OXYGENATED STEROIDS1 Journal of the American Chemical Society. 78: 501-502. DOI: 10.1021/Ja01583A073 |
0.338 |
|
| 1956 |
Stork G, Schulenberg JW. THE TOTAL SYNTHESIS OF dl-DEHYDROABIETIC ACID Journal of the American Chemical Society. 78: 250-251. DOI: 10.1021/Ja01582A070 |
0.405 |
|
| 1955 |
Stork G, Burgstahler AW. The Stereochemistry of Polyene Cyclization Journal of the American Chemical Society. 77: 5068-5077. DOI: 10.1021/Ja01624A038 |
0.492 |
|
| 1955 |
Stork G, Clarke FH. The Total Synthesis of Cedrol and Cedrene Journal of the American Chemical Society. 77: 1072-1073. DOI: 10.1021/Ja01609A104 |
0.496 |
|
| 1954 |
Stork G, Terrell R, Szmuszkovicz J. A NEW SYNTHESIS OF 2-ALKYL AND 2-ACYL KETONES Journal of the American Chemical Society. 76: 2029-2030. DOI: 10.1021/Ja01636A103 |
0.49 |
|
| 1953 |
Stork G, Breslow R. THE REARRANGEMENT OF BROMONORCEDRENEDICARBOXYLIC ACID Journal of the American Chemical Society. 75: 3292-3292. DOI: 10.1021/Ja01109A525 |
0.456 |
|
| 1953 |
Stork G, Breslow R. THE STRUCTURE OF CEDRENE Journal of the American Chemical Society. 75: 3291-3291. DOI: 10.1021/Ja01109A524 |
0.41 |
|
| 1953 |
Stork G, Wagle SS, Mukharji PC. Synthesis and Reactions of 1-Methyl-2-vinyl-4-hydroxycyclohexene Journal of the American Chemical Society. 75: 3197-3204. DOI: 10.1021/Ja01109A046 |
0.401 |
|
| 1953 |
Stork G, Tamelen EEv, Friedman LJ, Burgstahler AW. A Stereospecific Synthesis of Cantharidin Journal of the American Chemical Society. 75: 384-392. DOI: 10.1021/Ja01098A039 |
0.509 |
|
| 1952 |
Djerassi C, Mancera O, Velasco M, Stork G, Rosenkranz G. Steroids. XXXII.1Introduction of the 11-Keto and 11α-Hydroxy Groups into Ring C Unsubstituted Steroids (Part 5). Δ8-7-Ketones Journal of the American Chemical Society. 74: 3321-3323. DOI: 10.1021/Ja01133A030 |
0.45 |
|
| 1952 |
Romo J, Stork G, Rosenkranz G, Djerassi C. Steroids. XXXI.1Introduction of the 11-Keto and 11α-Hydroxy Groups into Ring C Unsubstituted Steroids (Part 4).2Saturated 7,11-Diones Journal of the American Chemical Society. 74: 2918-2920. DOI: 10.1021/Ja01131A060 |
0.438 |
|
| 1951 |
Stork G, Conroy H. The Synthesis of Some 1-Substituted 7,8-Dimethoxy-2-tetralones Journal of the American Chemical Society. 73: 4743-4748. DOI: 10.1021/Ja01154A079 |
0.518 |
|
| 1951 |
Stork G, Tamelen EEV, Friedman LJ, Burgstahler AW. CANTHARIDIN. A STEREOSPECIFIC TOTAL SYNTHESIS Journal of the American Chemical Society. 73: 4501-4501. DOI: 10.1021/Ja01153A552 |
0.501 |
|
| 1951 |
Djerassi C, Mancera O, Stork G, Rosenkranz G. STEROIDS. XXVIII.1INTRODUCTION OF THE 11-KETO AND 11α-HYDROXY GROUPS INTO RING C UNSUBSTITUTED STEROIDS (PART 2) Journal of the American Chemical Society. 73: 4496-4497. DOI: 10.1021/Ja01153A546 |
0.434 |
|
| 1951 |
Stork G, Burgstahler A. A NEW ROUTE TO HYDROPHENANTHRENE KETONES. THE SYNTHESIS OF THE C18KETONE DERIVED FROM DEHYDROABIETIC ACID Journal of the American Chemical Society. 73: 3544-3546. DOI: 10.1021/Ja01151A552 |
0.443 |
|
| 1948 |
Johnson WS, Davis CE, Hunt RH, Stork G. The Stobbe Condensation with Cyclohexanone Journal of the American Chemical Society. 70: 3021-3023. DOI: 10.1021/Ja01189A055 |
0.472 |
|
| 1947 |
STORK G. Sex hormones; a synthesis of 1-keto-7-methoxy-1,2,3,4-tetrahydrophenanthrene and of 1-keto-7-methoxy-1,2,3,4,9,10-hexahydrophenanthrene. Journal of the American Chemical Society. 69: 2936-9. PMID 18919697 DOI: 10.1021/Ja01204A004 |
0.397 |
|
| 1947 |
Stork G, McElvain SM. Preparation of Ethyl β-Benzylaminopropionate and Benzyl-di-(β-carbethoxyethyl)-amine Journal of the American Chemical Society. 69: 971-972. DOI: 10.1021/Ja01196A509 |
0.552 |
|
| 1947 |
Stork G. The Base Effect in Catalytic Hydrogenation. A Simple Synthesis of 6-Methoxy-α-tetralone Journal of the American Chemical Society. 69: 576-579. DOI: 10.1021/Ja01195A034 |
0.349 |
|
| 1946 |
STORK G, McELVAIN SM. Piperidine derivatives; C-alkylation of l-benzoyl-3-carbethoxy-4-piperidone; synthesis of ethyl 3-ethyl-4-piperidylacetate (d1-ethyl cincholoiponate). Journal of the American Chemical Society. 68: 1053-7. PMID 20985619 DOI: 10.1021/Ja01210A041 |
0.606 |
|
| 1946 |
McELVAIN SM, STORK G. Piperidine derivatives; the preparation of l-benzoyl-3-carbethoxy-4-piperidone; a synthesis of guvacine. Journal of the American Chemical Society. 68: 1049-53. PMID 20985618 DOI: 10.1021/Ja01210A040 |
0.619 |
|
| 1945 |
Stork G. THE SYNTHESIS OF 3,4-DIAMINOCARBETHOXYFURAN Journal of the American Chemical Society. 67: 884-884. DOI: 10.1021/Ja01221A511 |
0.504 |
|
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