Year |
Citation |
Score |
2010 |
Marshall JA, Griot CA, Chobanian HR, Myers WH. Synthesis of a lactone diastereomer of the cembranolide uprolide D. Organic Letters. 12: 4328-31. PMID 20795632 DOI: 10.1021/Ol101776E |
0.78 |
|
2010 |
MARSHALL JA. ChemInform Abstract: Palladium- and Platinum-Catalyzed Addition of Aldehydes and Imines with Allylstannanes. Chemoselective Allylation of Imines in the Presence of Aldehydes. Cheminform. 28: no-no. DOI: 10.1002/chin.199725280 |
0.37 |
|
2010 |
MARSHALL JA, BEAUDOIN S. ChemInform Abstract: Stereoselective Synthesis of Higher Sugars by Homologation of Carbohydrate-Derived Enals with Nonracemic γ-(Silyloxy) Allylic Stannanes and Substrate-Directed Hydroxylation. Cheminform. 26: no-no. DOI: 10.1002/chin.199520187 |
0.338 |
|
2010 |
MARSHALL JA, SELETSKY BM, COAN PS. ChemInform Abstract: Highly syn-Selective Additions of Allylic Stannanes to Protected . alpha.-Amino Aldehydes. Cheminform. 26: no-no. DOI: 10.1002/chin.199510260 |
0.757 |
|
2010 |
MARSHALL JA, WELMAKER GS. ChemInform Abstract: Enantioselective Synthesis of (+)- and (-)-Muricatacin Through SE2′ Addition of Nonracemic γ-Silyloxy Allylic Stannanes to Aldehydes. Cheminform. 26: no-no. DOI: 10.1002/chin.199504269 |
0.394 |
|
2010 |
MARSHALL JA, PINNEY KG. ChemInform Abstract: Stereoselective Synthesis of 2,5-Dihydrofurans by Sequential SN2′ Cleavage of Alkynyloxiranes and Ag+-Catalyzed Cyclization of the Allenylcarbinol Products. Cheminform. 25: no-no. DOI: 10.1002/chin.199416140 |
0.647 |
|
2010 |
MARSHALL JA. ChemInform Abstract: Synthesis of Cembranoid Natural Products by Intramolecular SE′ Additions of Allylic Stannanes to Ynals Cheminform. 23: no-no. DOI: 10.1002/chin.199233319 |
0.322 |
|
2009 |
Marshall JA. Synthesis and Reactions of Allenylzinc Reagents Patai's Chemistry of Functional Groups. 421-455. DOI: 10.1002/9780470682531.Pat0373 |
0.459 |
|
2008 |
Marshall JA, Hann RK. A cascade cyclization route to adjacent bistetrahydrofurans from chiral triepoxyfarnesyl bromides. The Journal of Organic Chemistry. 73: 6753-7. PMID 18683983 DOI: 10.1021/Jo801188W |
0.814 |
|
2008 |
Marshall JA, Eidam PM. A formal synthesis of the callipeltoside aglycone. Organic Letters. 10: 93-6. PMID 18052287 DOI: 10.1021/ol702024b |
0.736 |
|
2007 |
Marshall JA. Chiral allylic and allenic metal reagents for organic synthesis. The Journal of Organic Chemistry. 72: 8153-66. PMID 17595141 DOI: 10.1021/Jo070787C |
0.425 |
|
2007 |
Marshall JA, Sabatini JJ, Valeriote F. ABC synthesis and antitumor activity of a series of Annonaceous acetogenin analogs with a threo, trans, threo, trans, threo-bis-tetrahydrofuran core unit. Bioorganic & Medicinal Chemistry Letters. 17: 2434-7. PMID 17329102 DOI: 10.1016/J.Bmcl.2007.02.033 |
0.633 |
|
2007 |
Marshall J, Herold M, Eidam H, Eidam P. Pd- and Cu-Catalyzed 1,4-Addition of Dialkylzinc Compounds to α,β-Enals Synfacts. 2007: 0197-0197. DOI: 10.1055/s-2006-955806 |
0.769 |
|
2007 |
Marshall JA, Eidam P, Eidam HS. Synthesis of 4‐Triisopropylsilyl‐3‐Butyn‐2‐ol by Asymmetric Transfer Hydrogenation Organic Syntheses. 120-128. DOI: 10.1002/0471264229.Os084.12 |
0.796 |
|
2007 |
Marshall JA, Eidam P, Eidam HS. Synthesis of 4-triisopropylsilyl-3-butyn-2-ol by asymmetric transfer hydrogenation Organic Syntheses. 84: 120-128. |
0.78 |
|
2006 |
Marshall JA, Herold M, Eidam HS, Eidam P. Palladium- and copper-catalyzed 1,4-additions of organozinc compounds to conjugated aldehydes. Organic Letters. 8: 5505-8. PMID 17107058 DOI: 10.1021/Ol062154A |
0.798 |
|
2006 |
Marshall JA, Mikowski AM. Synthesis of a bistetrahydrofuran C17-C32 fragment of the polyether antibiotic ionomycin. Organic Letters. 8: 4375-8. PMID 16956230 DOI: 10.1021/Ol061826U |
0.8 |
|
2006 |
Marshall JA, Sabatini JJ. An outside-in approach to adjacent bistetrahydrofuran annonaceous acetogenins with C2 core symmetry. Total synthesis of asimicin and a C32 analogue. Organic Letters. 8: 3557-60. PMID 16869659 DOI: 10.1021/Ol061352Z |
0.68 |
|
2006 |
Marshall JA, Eidam P, Eidam HS. (R)- and (S)-4-TIPS-3-butyn-2-ol. Useful precursors of chiral allenylzinc and indium reagents. The Journal of Organic Chemistry. 71: 4840-4. PMID 16776511 DOI: 10.1021/Jo060542K |
0.82 |
|
2006 |
Marshall JA, Mikowski AM, Bourbeau MP, Schaaf GM, Valeriote F. Leptostatin: a synthetic hybrid of the cytotoxic polyketides callystatin A and leptomycin B. Bioorganic & Medicinal Chemistry Letters. 16: 320-3. PMID 16271470 DOI: 10.1016/J.Bmcl.2005.09.084 |
0.763 |
|
2006 |
Marshall J, Eidam P, Eidam H. Chiral Allenylzinc and Indium Reagents for Asymmetric Propargylation Synfacts. 2006: 0941-0941. DOI: 10.1055/s-2006-949218 |
0.801 |
|
2005 |
Marshall JA, Schaaf G, Nolting A. Synthesis of the C6-C21 segment of amphidinolide E. Organic Letters. 7: 5331-3. PMID 16268571 DOI: 10.1021/Ol0523493 |
0.669 |
|
2005 |
Marshall JA, Sabatini JJ. Synthesis of cis- and trans-2,5-disubstituted tetrahydrofurans by a tandem dihydroxylation-SN2 cyclization sequence. Organic Letters. 7: 4819-22. PMID 16235897 DOI: 10.1021/Ol051507N |
0.671 |
|
2005 |
Marshall JA, Mulhearn JJ. Synthesis of a C20-C26 segment of superstolide A by addition of a chiral allenylzinc reagent to (R)-N-boc alaninal. Organic Letters. 7: 1593-6. PMID 15816760 DOI: 10.1021/ol050289v |
0.309 |
|
2005 |
Marshall JA, Chobanian H. Lipase‐Catalyzed Resolution of 4‐Trimethylsilyl‐3‐Butyn‐2‐ol and Conversion of the (R)‐Enantiomer to (R)‐3‐Butyn‐2‐yl Mesylate and (P)‐1‐Tributylstannyl‐1,2‐Butadiene Organic Syntheses. 43-55. DOI: 10.1002/0471264229.Os082.07 |
0.725 |
|
2005 |
Marshall JA, Yanik MM, Adams ND, Ellis KC, Chobanian HR. Generation of Nonracemic 2‐(t‐Butyldimethylsilyloxy)‐3‐butynyllithium from (S)‐Ethyl Lactate: Organic Syntheses. 157-170. DOI: 10.1002/0471264229.Os081.17 |
0.647 |
|
2005 |
Marshall JA, Chobanian H. Lipase-catalyzed resolution of 4-trimethylsilyl-3-butyn-2-ol and conversion of the (R)-enantiomer to (R)-3-butyn-2-yl mesylate and (P)-1-tributylstannyl-1, 2-butadiene Organic Syntheses. 82: 43-54. |
0.674 |
|
2005 |
Marshall JA, Yanik MM, Adams ND, Ellis KC, Chobanian HR. Generation of nonracemic 2-(tbutyldimethylsilyloxy)-3-butynyllithium from (S)ethyl lactate Organic Syntheses. 81. |
0.76 |
|
2004 |
Marshall JA, Eidam P. Diastereoselective additions of chiral vinylzinc reagents to alpha-chiral aldehydes. Organic Letters. 6: 445-8. PMID 14748614 DOI: 10.1021/Ol0363568 |
0.747 |
|
2004 |
Marshall JA, Ellis K. Applications of chiral allenylzinc additions and Noyori asymmetric reductions to an enantioselective synthesis of a C3-C13 precursor of the polyketide phosphatase inhibitor cytostatin Tetrahedron Letters. 45: 1351-1353. DOI: 10.1016/J.Tetlet.2003.12.067 |
0.648 |
|
2003 |
Marshall JA, Schaaf GM. Total synthesis and structure confirmation of leptofuranin D. The Journal of Organic Chemistry. 68: 7428-32. PMID 12968896 DOI: 10.1021/Jo0348930 |
0.737 |
|
2003 |
Marshall JA, Bourbeau MP. Synthesis of enantioenriched propargylic alcohols related to polyketide natural products. A comparison of methodologies. Organic Letters. 5: 3197-9. PMID 12943386 DOI: 10.1021/Ol034918H |
0.771 |
|
2003 |
Marshall JA, Chobanian HR. Synthesis of 2,5-disubstituted tetrahydrofurans by stereospecific elimination-cyclization of 1-iodomethyl-1,5-bis-epoxides. Organic Letters. 5: 1931-3. PMID 12762689 DOI: 10.1021/Ol034509L |
0.746 |
|
2003 |
Marshall JA, Ellis KC. Total synthesis of (-)- and (+)-membrenone C. Organic Letters. 5: 1729-32. PMID 12735763 DOI: 10.1021/ol034367v |
0.626 |
|
2003 |
Marshall JA, Piettre A, Paige MA, Valeriote F. Total synthesis and structure confirmation of the annonaceous acetogenins 30(S)-hydroxybullatacin, uvarigrandin a, and 5(R)-uvarigrandin a (narumicin I?). The Journal of Organic Chemistry. 68: 1780-5. PMID 12608791 DOI: 10.1021/Jo0266137 |
0.796 |
|
2003 |
Marshall JA, Piettre A, Paige MA, Valeriote F. A modular synthesis of annonaceous acetogenins. The Journal of Organic Chemistry. 68: 1771-9. PMID 12608790 DOI: 10.1021/Jo026433X |
0.788 |
|
2003 |
Marshall JA, Bourbeau MP. Directed Pd(0)-catalyzed hydrostannations of internal alkynes Tetrahedron Letters. 44: 1087-1089. DOI: 10.1016/S0040-4039(02)02660-6 |
0.734 |
|
2003 |
Marshall JA, Garofalo AW, Hinkle KW. Synthesis of (S,E)‐1‐(Methoxymethoxy)‐1‐Tributylstannyl‐2‐Butene Organic Syntheses. 98-98. DOI: 10.1002/0471264180.Os077.10 |
0.378 |
|
2003 |
Marshall JA, Sehon CA. Isomerization of β‐Alkynyl Allylic Alcohols to Furans Catalyzed by Silver Nitrate on Silica Gel: 2‐Pentyl‐3‐Methyl‐5‐Heptylfuran Organic Syntheses. 76: 263-263. DOI: 10.1002/0471264180.Os076.26 |
0.435 |
|
2002 |
Marshall JA, Bourbeau MP. Second-generation synthesis of the polypropionate subunit of callystatin A based on regioselective internal alkyne hydrostannation. Organic Letters. 4: 3931-4. PMID 12599495 DOI: 10.1021/Ol026791M |
0.761 |
|
2002 |
Marshall JA, Bourbeau MP. Total synthesis of (-)-callystatin A. The Journal of Organic Chemistry. 67: 2751-4. PMID 11975524 DOI: 10.1021/Jo016025D |
0.753 |
|
2002 |
Marshall JA, Adams ND. Total synthesis of bafilomycin V(1): a methanolysis product of the macrolide bafilomycin C(2). The Journal of Organic Chemistry. 67: 733-40. PMID 11856013 DOI: 10.1021/Jo015864X |
0.718 |
|
2002 |
Johns BA, Grant CM, Marshall JA, Holson EB, Roush WR. Synthesis and utilization of indium (i) iodide for in situ formation of enantioenriched allenylindium reagents and their addition to aldehydes: (2r,3s,4s)-1-(tertbutyldiphenylsilyloxy)-2,4-dimethyl-5-hexyn-3-ol Organic Syntheses. 79: 59-70. DOI: 10.1002/0471264180.Os079.08 |
0.597 |
|
2001 |
Marshall JA, Chobanian HR, Yanik MM. Coupling of alkynylTMS derivatives with vinylic iodides. An efficient route to 1,3-enynes and dienes. Organic Letters. 3: 4107-10. PMID 11735596 DOI: 10.1021/Ol016899M |
0.804 |
|
2001 |
Marshall JA, Van Devender EA. Synthesis of (-)-deoxypukalide, the enantiomer of a degradation product of the furanocembranolide pukalide. The Journal of Organic Chemistry. 66: 8037-41. PMID 11722202 DOI: 10.1021/jo016048s |
0.815 |
|
2001 |
Marshall JA, Schaaf GM. Synthesis of stereopentad analogues of the C14-C22 segment of callystatin A through additions of chiral allenylzinc reagents to stereotriads. The Journal of Organic Chemistry. 66: 7825-31. PMID 11701042 DOI: 10.1021/Jo015936K |
0.692 |
|
2001 |
Marshall JA, Chobanian HR, Yanik MM. Lipase-mediated resolution of 4-TMS-3-butyn-2-ol and use of the mesylate derivatives as a precursor to a highly stereoselective chiral allenylindium reagent. Organic Letters. 3: 3369-72. PMID 11594836 DOI: 10.1021/Ol016605X |
0.793 |
|
2001 |
Marshall JA, Yanik MM. Synthesis of a C1-C21 subunit of the protein phosphatase inhibitor tautomycin: a formal total synthesis. The Journal of Organic Chemistry. 66: 1373-9. PMID 11312969 DOI: 10.1021/jo0056951 |
0.658 |
|
2001 |
Cossy J, Rasamison C, Pardo DG, Marshall JA. Solid-support synthesis of 1,2-diols and γ-lactones through addition of α-(benzoyloxy)crotylindium reagents to aldehydes Synlett. 629-633. DOI: 10.1055/S-2001-13367 |
0.403 |
|
2001 |
Marshall JA, Yanik MM. CorrigendumCorrigendum to “Stereoselective synthesis of substituted ketopyranose subunits of polyketide natural products by intramolecular alkoxycarbonylation of δ-alkynyl alcohols”: [Tetrahedron Letters 41 (2000) 4717–4721] Tetrahedron Letters. 42: 2243. DOI: 10.1016/S0040-4039(01)00026-0 |
0.422 |
|
2001 |
Marshall JA, Gill K. The BF3 and B(C6F5)3-catalyzed 1,3-isomerization of allylic stannanes Journal of Organometallic Chemistry. 624: 294-299. DOI: 10.1016/S0022-328X(01)00642-8 |
0.596 |
|
2000 |
Marshall JA. Synthesis and Reactions of Allylic, Allenic, Vinylic, and Arylmetal Reagents from Halides and Esters via Transient Organopalladium Intermediates. Chemical Reviews. 100: 3163-86. PMID 11749316 DOI: 10.1021/Cr000003U |
0.455 |
|
2000 |
Marshall JA, Chobanian HR. Additions of enantioenriched allenylzinc and indium reagents to lactic aldehyde ethers The Journal of Organic Chemistry. 65: 8357-60. PMID 11101396 |
0.722 |
|
2000 |
Marshall JA, Adams ND. Progress toward the total synthesis of bafilomycin A(1): stereoselective synthesis of the C15-C25 subunit by additions of nonracemic allenylzinc reagents to aldehydes. Organic Letters. 2: 2897-900. PMID 10964393 DOI: 10.1021/Ol006344B |
0.713 |
|
2000 |
Marshall JA, Yanik MM. Synthesis of beta-hydroxy ketones and vinylsilanes from homopropargylic alcohols by intramolecular hydrosilation Organic Letters. 2: 2173-5. PMID 10891259 |
0.574 |
|
2000 |
Marshall JA, Johns BA. Stereoselective synthesis of C5-C20 and C21-C34 subunits of the core structure of the aplyronines. Applications of enantioselective additions of chiral allenylindium reagents to chiral aldehydes. The Journal of Organic Chemistry. 65: 1501-10. PMID 10814114 DOI: 10.1021/Jo991689X |
0.459 |
|
2000 |
Marshall JA, Maxson K. Stereoselective synthesis of stereotriad subunits of polyketides through additions of nonracemic allenylsilanes to (R)- and (S)-2-methyl-3-oxygenated propanals The Journal of Organic Chemistry. 65: 630-3. PMID 10813988 DOI: 10.1021/Jo991543Y |
0.803 |
|
2000 |
Marshall JA, Gill K, Seletsky BM. Addition of Enantioenriched gamma-Oxygenated Allylic Stannanes to N-Acyl Iminium Intermediates: A New Synthesis of syn-Amino Alcohol Derivatives This research was supported by the National Institute of Allergy and Infectious Diseases (grant R01 AI31422). Angewandte Chemie (International Ed. in English). 39: 953-956. PMID 10760905 DOI: 10.1002/(Sici)1521-3773(20000303)39:5<953::Aid-Anie953>3.0.Co;2-I |
0.805 |
|
2000 |
Marshall JA, Chobanian HR. Additions of enantioenriched alenylzinc and indium reagents to lactic aldehyde ethers Journal of Organic Chemistry. 65: 8357-8360. DOI: 10.1021/jo005658+ |
0.752 |
|
2000 |
Marshall JA. Synthesis and reactions of allylic, allenic, vinylic, and arylmetal reagents from halides and esters via transient organopalladium intermediates Chemical Reviews. 100: 3163-3185. DOI: 10.1021/cr000003u |
0.346 |
|
2000 |
Marshall JA, Zou D. A new synthesis of 3-carboxy-2,5-disubstituted furans and their conversion to 5-vinyl derivatives Tetrahedron Letters. 41: 1347-1350. DOI: 10.1016/S0040-4039(99)02290-X |
0.391 |
|
2000 |
Marshall JA, Yanik MM. Stereoselective synthesis of substituted ketopyranose subunits of polyketide natural products by intramolecular alkoxycarbonylation of δ- alkynyl alcohols Tetrahedron Letters. 41: 4717-4721. DOI: 10.1016/S0040-4039(00)00705-X |
0.655 |
|
2000 |
Marshall JA, Garofalo AW, Hinkle KW. Synthesis of (S,E)-1-(methoxymethoxy)-1-tributylstannyl-2-bytene: (Stannane, tributyl[1-(methoxymethoxy)-2-butenyl]-, [S-(E)]-) Organic Syntheses. 77: 98-105. |
0.502 |
|
2000 |
Marshall JA, Yanik MM. Synthesis of β-hydroxy ketones and vinylsilanes from homopropargylic alcohols by intramolecular hydrosilation Organic Letters. 2: 2173-2175. |
0.576 |
|
2000 |
Marshall JA. Umpolung of chiral 2-ethynylaziridines: Indium(I)-mediated stereoselective synthesis of nonracemic 1,3-amino alcohols bearing three chiral centers, catalyzed by palladium(0) Chemtracts. 13: 616-619. |
0.343 |
|
1999 |
Marshall JA, Adams ND. Addition of Allenylzinc Reagents, Prepared in Situ from Nonracemic Propargylic Mesylates, to Aldehydes. A New Synthesis of Highly Enantioenriched Homopropargylic Alcohols. The Journal of Organic Chemistry. 64: 5201-5204. PMID 34237878 DOI: 10.1021/jo9823083 |
0.668 |
|
1999 |
Marshall JA, Adams ND. Addition of Allenylzinc Reagents, Prepared in Situ from Nonracemic Propargylic Mesylates, to Aldehydes. A New Synthesis of Highly Enantioenriched Homopropargylic Alcohols. The Journal of Organic Chemistry. 64: 5201-5204. PMID 34237878 DOI: 10.1021/jo9823083 |
0.308 |
|
1999 |
Marshall JA, McNulty LM, Zou D. Synthesis of Pseudopterane Analogues by Intramolecular S2' Cyclization. The Journal of Organic Chemistry. 64: 5193-5200. PMID 34237855 DOI: 10.1021/jo990376z |
0.742 |
|
1999 |
Marshall JA, Grant CM. Preparation of Chiral Allenylmetal Reagents from Enantioenriched Allenyl Iodides and Propargylic Mesylates. A Comparison of Indium, Bismuth, and Tin Derivatives. The Journal of Organic Chemistry. 64: 8214-8219. PMID 11674739 DOI: 10.1021/Jo990938E |
0.648 |
|
1999 |
Marshall JA, Jablonowski JA, Jiang H. Total Synthesis of the Gypsy Moth Pheromones (+)- and (-)-Disparlure from a Single Nonracemic alpha-Silyloxy Allylic Stannane. The Journal of Organic Chemistry. 64: 2152-2154. PMID 11674319 DOI: 10.1021/Jo982353A |
0.774 |
|
1999 |
Marshall JA, Jiang H. Total Synthesis of the Cytotoxic Threo, Trans, Erythro, Cis, Threo Annonaceous Acetogenin Trilobin. The Journal of Organic Chemistry. 64: 971-975. PMID 11674171 DOI: 10.1021/Jo982057Y |
0.567 |
|
1999 |
Marshall JA, Grant CM. Formation of Transient Chiral Allenylindium Reagents from Enantioenriched Propargylic Mesylates through Oxidative Transmetalation. Applications to the Synthesis of Enantioenriched Homopropargylic Alcohols. The Journal of Organic Chemistry. 64: 696-697. PMID 11674133 DOI: 10.1021/Jo982255P |
0.597 |
|
1999 |
Marshall JA, Jiang H. Total synthesis of the cytotoxic threo, trans, threo, trans, threo annonaceous acetogenin asimin and its C-10 epimer: unambiguous confirmation of absolute stereochemistry. Journal of Natural Products. 62: 1123-7. PMID 10479317 DOI: 10.1021/Np990132+ |
0.555 |
|
1999 |
Marshall JA, Yanik MM. Synthesis of nonracemic β-hydroxy ketones and carbonate derivatives from homopropargylic alcohols through iodolactonization Journal of Organic Chemistry. 64: 3798-3799. DOI: 10.1021/Jo990439D |
0.611 |
|
1999 |
Marshall JA, McNulty LM, Zou D. Synthesis of pseudopterane analogues by intramolecular S(E)2' cyclization Journal of Organic Chemistry. 64: 5193-5200. DOI: 10.1021/Jo990376Z |
0.754 |
|
1999 |
Marshall JA, Fitzgerald RN. Synthesis of a syn,syn,syn,syn-stereopentad precursor of the marine sponge polyketide callystatin A Journal of Organic Chemistry. 64: 4477-4481. DOI: 10.1021/Jo9902143 |
0.484 |
|
1999 |
Marshall JA, Jablonowski JA, Jiang H. Total synthesis of the gypsy moth pheromones (+)- and (-)-disparlure from a single nonracemic α-silyloxy allylic stannane Journal of Organic Chemistry. 64: 2152-2154. DOI: 10.1021/jo982353a |
0.777 |
|
1999 |
Marshall JA, Adams ND. Addition of allenylzinc reagents, prepared in situ from nonracemic propargylic mesylates, to aldehydes. A new synthesis of highly enantioenriched homopropargylic alcohols Journal of Organic Chemistry. 64: 5201-5204. DOI: 10.1021/Jo9823083 |
0.693 |
|
1999 |
Marshall JA, Sehon CA. Isomerization of β-alkynyl allylic alcohols to furans catalyzed by silver nitrate on silica gel: 2-pentyl-3-methyl-5-heptylfuran Organic Syntheses. 76: 263-269. |
0.717 |
|
1998 |
Marshall JA, Jiang H. Total Synthesis of the Nonadjacent Bis-Tetrahydrofuran Annonaceous Acetogenin Squamostatin-D. The Journal of Organic Chemistry. 63: 7066-7071. PMID 11672333 DOI: 10.1021/Jo981103R |
0.625 |
|
1998 |
Marshall JA, Liao J. Stereoselective Total Synthesis of the Pseudopterolide Kallolide A. The Journal of Organic Chemistry. 63: 5962-5970. PMID 11672200 DOI: 10.1021/Jo980603H |
0.471 |
|
1998 |
Marshall JA, Lu ZH, Johns BA. Synthesis of Discodermolide Subunits by S(E)2' Addition of Nonracemic Allenylstannanes to Aldehydes. The Journal of Organic Chemistry. 63: 817-823. PMID 11672079 DOI: 10.1021/Jo971900+ |
0.573 |
|
1998 |
Marshall JA, Johns BA. Total synthesis of (+)-discodermolide Journal of Organic Chemistry. 63: 7885-7892. DOI: 10.1021/jo9811423 |
0.311 |
|
1998 |
Marshall JA, Adams ND. Synthesis of Chiral Enantioenriched Homopropargylic Alcohols from Propargylic Mesylates via Chiral Allenylzinc Intermediates Journal of Organic Chemistry. 63: 3812-3813. DOI: 10.1021/Jo980623J |
0.692 |
|
1998 |
Marshall JA, Palovich MR. Enantioselective and Diastereoselective Additions of Allylic Stannanes to Aldehydes Promoted by a Chiral (Acyloxy)borane Catalyst Journal of Organic Chemistry. 63: 4381-4384. DOI: 10.1021/Jo980145C |
0.769 |
|
1998 |
Marshall JA, Palovich MR. Synthesis of Stereopentad Subunits of Zincophorin and Rifamycin-S through Use of Chiral Allenyltin Reagents Journal of Organic Chemistry. 63: 3701-3705. DOI: 10.1021/Jo980137W |
0.797 |
|
1998 |
Marshall JA, Jiang H. Total synthesis of the threo, trans, threo-mono-tetrahydrofuran annonaceous acetogenin longifolicin Tetrahedron Letters. 39: 1493-1496. DOI: 10.1016/S0040-4039(98)00007-0 |
0.621 |
|
1998 |
Marshall JA, Hinkle KW. Total synthesis of the cytotoxic annonaceous acetogenin (30S)-bullanin Tetrahedron Letters. 39: 1303-1306. DOI: 10.1016/S0040-4039(97)10739-0 |
0.636 |
|
1998 |
Marshall JA. Stereo- and enantioselective additions of allylic, propargylic, and allenic trihalosilanes to aldehydes Chemtracts. 11: 697-712. |
0.387 |
|
1998 |
Marshall JA, Lu ZH, Johns BA. Synthesis of Discodermolide Subunits by SE2′ Addition of Nonracemic Allenylstannanes to Aldehydes Journal of Organic Chemistry. 63: 817-823. |
0.328 |
|
1997 |
Marshall JA, Sehon CA. Total Synthesis of the Enantiomer of the Furanocembrane Rubifolide. The Journal of Organic Chemistry. 62: 4313-4320. PMID 11671752 DOI: 10.1021/Jo970360D |
0.765 |
|
1997 |
Marshall JA, Wolf MA, Wallace EM. Synthetic Routes to Allenic Acids and Esters and Their Stereospecific Conversion to Butenolides. The Journal of Organic Chemistry. 62: 367-371. PMID 11671411 DOI: 10.1021/Jo9618740 |
0.709 |
|
1997 |
Marshall JA, Adams ND. Diastereoselective and Enantioselective Synthesis of Homopropargyl and Allenylcarbinols from Nonracemic Propargyl Mesylates via the Derived Allenyl and Propargyl Trichlorosilanes The Journal of Organic Chemistry. 62: 8976-8977. DOI: 10.1021/Jo971853L |
0.728 |
|
1997 |
Marshall JA, Palovich MR. Comparative Studies on the Synthesis of an anti,syn Stereotriad with Chiral Allenylstannane and Allenylindium Reagents Journal of Organic Chemistry. 62: 6001-6005. DOI: 10.1021/Jo970650U |
0.761 |
|
1997 |
Marshall JA, Chen M. Total Synthesis of the Annonaceous Acetogenins Asiminocin and Asiminecin by a Bidirectional Approach Journal of Organic Chemistry. 62: 5996-5997. DOI: 10.1021/Jo970424K |
0.772 |
|
1997 |
Marshall JA, Hinkle KW. Total synthesis of the Annonaceous acetogenin (+)-asimicin. Development of a new bidirectional strategy Journal of Organic Chemistry. 62: 5989-5995. DOI: 10.1021/Jo970423S |
0.666 |
|
1997 |
Marshall JA, Hinkle KW, Hagedorn CE. Recent developments in the synthesis of annonaceous acetogenins Israel Journal of Chemistry. 37: 97-107. DOI: 10.1002/Ijch.199700012 |
0.595 |
|
1997 |
Marshall JA. Additions of allylic indium reagents to aldehydes Chemtracts. 10: 481-496. |
0.376 |
|
1996 |
Marshall JA. Chiral Allylic and Allenic Stannanes as Reagents for Asymmetric Synthesis. Chemical Reviews. 96: 31-48. PMID 11848743 |
0.373 |
|
1996 |
Marshall JA, Hinkle KW. Stereoselective S(E)2' Additions of Enantioenriched Allylic Tin and Indium Reagents to Protected Threose and Erythrose Aldehydes: A General Strategy for the Stereocontrolled Synthesis of Precursors to the Eight Diastereomeric Hexoses and Their Enantiomers. The Journal of Organic Chemistry. 61: 9072. PMID 11667908 DOI: 10.1021/Jo9640231 |
0.637 |
|
1996 |
Marshall JA, Garofalo AW. Synthesis of Chiral alpha,delta-Dioxygenated Allylic Stannanes as Reagents for Carbohydrate Synthesis and Homologation. The Journal of Organic Chemistry. 61: 8732-8738. PMID 11667845 DOI: 10.1021/Jo961671B |
0.674 |
|
1996 |
Marshall JA, Elliott LM. Methyl 2,3,4-Tri-O-benzyl-alpha-D-glucopyranosyl-Derived gamma-Silyloxy Allylic Stannanes as Reagents for S(E)2' Additions to Aldehydes. The Journal of Organic Chemistry. 61: 4611-4616. PMID 11667388 |
0.326 |
|
1996 |
Marshall JA, Hinkle KW. An Efficient Bidirectional Approach to the C(2)-Symmetric Stereoisomers of the Bistetrahydrofuran Core of the Acetogenins. The Journal of Organic Chemistry. 61: 4247-4251. PMID 11667322 DOI: 10.1021/Jo9603789 |
0.567 |
|
1996 |
Marshall JA, Jablonowski JA, Welmaker GS. On the Relative Reactivities of Allyl, Crotyl, alpha-Oxygenated Crotyl, gamma-Oxygenated alpha-Methylallyl, and Allenyl Tri-n-butylstannane Reagents in Lewis Acid Promoted Additions to Aldehydes. The Journal of Organic Chemistry. 61: 2904-2907. PMID 11667135 DOI: 10.1021/Jo9519975 |
0.775 |
|
1996 |
Marshall JA, Beaudoin S. Stereoselective Synthesis of Differentially Protected Derivatives of the Higher Amino Sugars Destomic Acid and Lincosamine from Serine and Threonine. The Journal of Organic Chemistry. 61: 581-586. PMID 11666978 DOI: 10.1021/Jo9517914 |
0.644 |
|
1996 |
Marshall JA, Bartley GS, Wallace EM. Total synthesis of the pseudopterane (-)-kallolide B, the enantiomer of natural (+)-kallolide B Journal of Organic Chemistry. 61: 5729-5735. DOI: 10.1021/Jo960798Y |
0.735 |
|
1996 |
Marshall JA, Wolf MA. Amination, aminocarbonylation, and alkoxycarbonylation of allenic/propargylic Pd intermediates derived from nonracemic propargylic mesylates: Synthesis of nonracemic propargyl amines, allenic amides, and butenolides Journal of Organic Chemistry. 61: 3238-3239. DOI: 10.1021/Jo960442M |
0.585 |
|
1996 |
Marshall JA, Hinkle KW. An efficient bidirectional approach to the C2-symmetric stereoisomers of the bistetrahydrofuran core of the acetogenins Journal of Organic Chemistry. 61: 4247-4251. DOI: 10.1021/jo9603789 |
0.495 |
|
1996 |
Marshall JA, Garofalo AW. Synthesis of Chiral α,δ-Dioxygenated Allylic Stannanes as Reagents for Carbohydrate Synthesis and Homologation Journal of Organic Chemistry. 61: 8732-8738. |
0.357 |
|
1996 |
Marshall JA, Jablonowski JA, Welmaker GS. On the relative reactivities of allyl, crotyl, α-oxygenated crotyl, γ-oxygenated α-methylallyl, and allenyl tri-n-butylstannane reagents in Lewis acid promoted additions to aldehydes Journal of Organic Chemistry. 61: 2904-2907. |
0.782 |
|
1996 |
Marshall JA, Hinkle KW. Stereoselective SE2′ additions of enantioenriched allylic tin and indium reagents to protected threose and erythrose aldehydes: A general strategy for the stereocontrolled synthesis of precursors to the eight diastereomeric hexoses and their enantiomers Journal of Organic Chemistry. 61: 105-108. |
0.633 |
|
1995 |
Marshall JA, Xie S. Synthesis of a C22-34 Subunit of the Immunosuppressant FK-506 Journal of Organic Chemistry. 60: 7230-7237. DOI: 10.1021/Jo00127A031 |
0.381 |
|
1995 |
Marshall JA, Sehon CA. Synthesis of Furans and 2,5-Dihydrofurans by Ag(I)-Catalyzed Isomerization of Allenones, Alkynyl Allylic Alcohols, and Allenylcarbinols Journal of Organic Chemistry. 60: 5966-5968. DOI: 10.1021/Jo00123A040 |
0.385 |
|
1995 |
Marshall JA, Perkins JF, Wolf MA. Synthesis of syn,syn; anti,syn; syn,anti; and anti,anti stereotriads from a single pair of enantiomeric reagents The Journal of Organic Chemistry. 60: 5556-5559. DOI: 10.1021/Jo00122A041 |
0.522 |
|
1995 |
Marshall JA, Yu RH, Perkins JF. Diastereo- and enantioselective synthesis of allenylcarbinols through SE2′ addition of transient nonracemic propargylic stannanes to aldehydes The Journal of Organic Chemistry. 60: 5550-5555. DOI: 10.1021/Jo00122A040 |
0.495 |
|
1995 |
Marshall JA, Jablonowski JA, Elliott LM. Interconversion of Nonracemic .alpha.-OTBS Crotyl and .gamma.-OTBS Methallyl Tri-n-butylstannanes. Additions of the (E)-Methallyl Isomer to Representative Aldehydes The Journal of Organic Chemistry. 60: 2662-2663. DOI: 10.1021/Jo00114A009 |
0.71 |
|
1995 |
Marshall JA, Bennett CE. Synthesis of Furans by SN2' Cyclization of .gamma.-Alkynyl Allylic Alcohol Derivatives. [Erratum to document cited in CA122:31231] The Journal of Organic Chemistry. 60: 2644-2644. DOI: 10.1021/Jo00113A060 |
0.373 |
|
1995 |
Marshall JA, Hinkle KW. Synthesis of anti-homoallylic alcohols and monoprotected 1,2-diols through InCl3-promoted addition of allylic stannanes to aldehydes Journal of Organic Chemistry. 60: 1920-1921. DOI: 10.1021/Jo00112A005 |
0.619 |
|
1995 |
Marshall JA, Wallace EM, Coan PS. Total Synthesis of the Pseudopterane (.+-.)-Kallolide B Journal of Organic Chemistry. 60: 796-797. DOI: 10.1021/Jo00109A007 |
0.345 |
|
1995 |
Marshall JA, Wallace EM, Coan PS. Total synthesis of the pseudopterane (±)-kallolide B The Journal of Organic Chemistry. 60: 796-797. |
0.489 |
|
1995 |
Marshall JA, Jablonowski JA, Elliott LM. Interconversion of nonracemic α-OTBS crotyl and γ-OTBS methallyl tri-n-butylstannanes. Additions of the (E)-methallyl isomer to representative aldehydes Journal of Organic Chemistry. 60: 2662-2663. |
0.699 |
|
1994 |
Marshall JA, Beaudoin S. Remote Conformational Bias Effects on Diastereofacial Selectivity in SE2' Additions of .gamma.-Oxygenated Allylic Stannanes to Chiral Enals Journal of Organic Chemistry. 59: 7833-7838. DOI: 10.1021/Jo00104A047 |
0.305 |
|
1994 |
Marshall JA, Beaudoin S. Stereoselective Synthesis of Higher Sugars by Homologation of Carbohydrate-Derived Enals with Nonracemic .gamma.-(Silyloxy) Allylic Stannanes and Substrate-Directed Hydroxylation Journal of Organic Chemistry. 59: 6614-6619. DOI: 10.1021/Jo00101A020 |
0.422 |
|
1994 |
Marshall JA, Bennett CE. Synthesis of Furans by SN2' Cyclization of .gamma.-Alkynyl Allylic Alcohol Derivatives The Journal of Organic Chemistry. 59: 6110-6113. DOI: 10.1021/Jo00099A054 |
0.41 |
|
1994 |
Marshall JA, Seletsky BM, Coan PS. Highly syn-Selective Additions of Allylic Stannanes to Protected .alpha.-Amino Aldehydes The Journal of Organic Chemistry. 59: 5139-5140. DOI: 10.1021/Jo00097A011 |
0.779 |
|
1994 |
Marshall JA, Welmaker GS. Enantioselective Synthesis of (+)- and (-)-Muricatacin through SE2' Addition of Nonracemic .gamma.-Silyloxy Allylic Stannanes to Aldehydes Journal of Organic Chemistry. 59: 4122-4125. DOI: 10.1021/Jo00094A023 |
0.356 |
|
1994 |
Marshall JA, Perkins J. Synthesis of Syn and Anti Homopropargylic and Allenic Alcohols through Diastereoselective SE2' Addition of a Common Chiral Allenylstannane Precursor to Aldehydes Journal of Organic Chemistry. 59: 3509-3511. DOI: 10.1021/Jo00092A001 |
0.438 |
|
1994 |
Marshall JA, Seletsky BM, Luke GP. Synthesis of Protected Carbohydrate Derivatives Through Homologation of Threose and Erythrose Derivatives with Chiral .gamma.-Alkoxy Allylic Stannanes Journal of Organic Chemistry. 59: 3413-3420. DOI: 10.1021/Jo00091A034 |
0.436 |
|
1994 |
Marshall JA, DuBay WJ. Synthesis of the Pseudopterane and Furanocembrane Ring Systems by Intraannular Cyclization of .beta.- and .gamma.-Alkynyl Allylic Alcohols Journal of Organic Chemistry. 59: 1703-1708. DOI: 10.1021/Jo00086A018 |
0.374 |
|
1994 |
Marshall JA, Tang Y. Enantioselective synthesis of carbohydrate precursors via 1,2:2,3-bis-epoxide intermediates Journal of Organic Chemistry. 59: 1457-1464. DOI: 10.1021/Jo00085A038 |
0.429 |
|
1994 |
Marshall JA, Yu B. Synthesis of the pseudopterane 2,5-furanocyclic ring system by [2,3] Wittig ring contraction of bridged furan and dihydrofuran propargylic ethers Journal of Organic Chemistry. 59: 324-331. DOI: 10.1021/Jo00081A009 |
0.425 |
|
1993 |
Marshall JA, DuBay WJ. A new synthesis of thiophenes through base-promoted cyclization of β- and γ-alkynyl thiols Synlett. 1993: 209-210. DOI: 10.1055/S-1993-22404 |
0.359 |
|
1993 |
Marshall JA, Pinney KG. Stereoselective synthesis of 2,5-dihydrofurans by sequential SN2' cleavage of alkynyloxiranes and silver(I)-catalyzed cyclization of the allenylcarbinol products Journal of Organic Chemistry. 58: 7180-7184. DOI: 10.1021/Jo00077A048 |
0.622 |
|
1993 |
Marshall JA, Luke GP. Stereoselective total synthesis of bengamide E from glyceraldehyde acetonide and a nonracemic .gamma.-alkoxy allylic stannane Journal of Organic Chemistry. 58: 6229-6234. DOI: 10.1021/Jo00075A017 |
0.439 |
|
1993 |
Marshall JA, Beaudoin S, Lewinski K. Stereoselective synthesis of long-chain polyols by sequential homologation of enals with nonracemic .gamma.-silyloxy allylic stannanes and directed hydroxylation Journal of Organic Chemistry. 58: 5876-5877. DOI: 10.1021/Jo00074A004 |
0.386 |
|
1993 |
Marshall JA, Andersen MW. Synthesis of 12-, 14-, and 16-membered propargylic alcohols through Lewis acid-promoted ene cyclization Journal of Organic Chemistry. 58: 3912-3918. DOI: 10.1021/Jo00067A024 |
0.42 |
|
1993 |
Marshall JA, Garofalo AW. Oxidative cleavage of mono-, di-, and trisubstituted olefins to methyl esters through ozonolysis in methanolic sodium hydroxide Journal of Organic Chemistry. 58: 3675-3680. DOI: 10.1021/Jo00066A019 |
0.365 |
|
1993 |
Marshall JA, DuBay WJ. Synthesis of rosefuran. A new route to furans through base-catalyzed cyclization of hydroxy alkynoates and alkynones Journal of Organic Chemistry. 58: 3602-3603. DOI: 10.1021/Jo00066A003 |
0.465 |
|
1993 |
Marshall JA, DuBay WJ. Synthesis of furans by base-catalyzed cyclization-isomerization of .beta.- and .gamma.-alkynyl allylic alcohols Journal of Organic Chemistry. 58: 3435-3443. DOI: 10.1021/Jo00064A038 |
0.418 |
|
1993 |
Marshall JA, Tang Y. Allene-directed diastereoselection. Additions to chiral allenyl aldehydes and ketones Journal of Organic Chemistry. 58: 3233-3234. DOI: 10.1021/Jo00064A006 |
0.313 |
|
1992 |
Marshall JA, Luke GP. Stereoselective Synthesis of a Bengamide E Derivative Through SE′ Addition of a Chiral γ-Alkoxy Allylic Stannane to a Tartrate-Derived α, β-Dialkoxy Aldehyde Synlett. 1992: 1007-1008. DOI: 10.1055/S-1992-21565 |
0.415 |
|
1992 |
Marshall JA, Tang Y. Catalyzed Asymmetric SE′ Addition of Allylstannanes to Aldehydes Synlett. 1992: 653-654. DOI: 10.1055/S-1992-21445 |
0.437 |
|
1992 |
Marshall JA, Garofalo AW, Sedrani RC. The direct conversion of olefins into esters through ozonolysis Synlett. 1992: 643-645. DOI: 10.1055/S-1992-21441 |
0.357 |
|
1992 |
Marshall JA, Welmaker GS. Stereoselective synthesis of the cytotoxic acetogenins (+)- and (-)-muricatacin Synlett. 1992: 537-538. DOI: 10.1055/S-1992-21408 |
0.461 |
|
1992 |
Marshall JA, Welmaker GS. (Z)- and (E)-.gamma.-silyloxy allylic stannanes. Highly syn selective reagents for SE' additions to aldehydes Journal of Organic Chemistry. 57: 7158-7163. DOI: 10.1021/Jo00052A033 |
0.327 |
|
1992 |
Marshall JA, Andersen MW. On the mechanism of Lewis acid promoted ene cyclizations of .omega.-unsaturated aldehydes The Journal of Organic Chemistry. 57: 5851-5856. DOI: 10.1021/Jo00048A016 |
0.426 |
|
1992 |
Marshall JA, Wang XJ. Synthesis of 2,5-furanocycles through intraannular cyclization of macrocyclic allenones Journal of Organic Chemistry. 57: 3387-3396. DOI: 10.1021/Jo00038A029 |
0.346 |
|
1992 |
Marshall JA, Xie S. An enantioselective synthesis of the spirotetronate subunit of kijanolide Journal of Organic Chemistry. 57: 2987-2989. DOI: 10.1021/Jo00037A005 |
0.418 |
|
1992 |
Marshall JA, Andersen MW. Synthesis of macrocyclic propargylic alcohols by ene-type cyclization of unsaturated acetylenic aldehydes Journal of Organic Chemistry. 57: 2766-2768. DOI: 10.1021/Jo00036A002 |
0.4 |
|
1992 |
Marshall JA, Wang XJ. Chiral base-induced [2,3] Wittig rearrangement of acyclic .alpha.-(propargyloxy)acetic acids and amides Journal of Organic Chemistry. 57: 2747-2750. DOI: 10.1021/Jo00035A041 |
0.342 |
|
1992 |
Marshall JA, Wang XJ. Synthesis of enantioenriched homopropargylic alcohols through diastereoselective SE' additions of chiral allenylstannanes to aldehydes Journal of Organic Chemistry. 57: 1242-1252. DOI: 10.1021/Jo00030A036 |
0.384 |
|
1992 |
Marshall JA, DuBay WJ. Base-catalyzed isomerization of alkynyloxiranes. A general synthesis of furans Journal of the American Chemical Society. 114: 1450-1456. DOI: 10.1021/Ja00030A047 |
0.42 |
|
1991 |
Marshall JA, Wang XJ. Synthesis of macrocyclic homopropargylic alcohols through intramolecular SE' addition of allenylstannanes and their subsequent conversion to 2,5-furanocycles Journal of Organic Chemistry. 56: 6264-6266. DOI: 10.1021/Jo00022A008 |
0.391 |
|
1991 |
Marshall JA, Sedrani R. A convergent, highly stereoselective synthesis of a C-11-C-21 subunit of the macbecins Journal of Organic Chemistry. 56: 5496-5498. DOI: 10.1021/Jo00019A004 |
0.364 |
|
1991 |
Marshall JA, Yashunsky DV. Highly stereoselective SE' additions of .alpha.-alkoxy allylstannanes to chiral aldehydes. Synthesis of a C-1-C-9 subunit of tylonolide Journal of Organic Chemistry. 56: 5493-5495. DOI: 10.1021/Jo00019A003 |
0.413 |
|
1991 |
Marshall JA, Wang XJ. Synthesis of enantioenriched .alpha.-hydroxy-.alpha.-allenylacetic acids by [2,3] Wittig rearrangement of .alpha.-(propargyloxy)acetates The Journal of Organic Chemistry. 56: 4913-4918. DOI: 10.1021/Jo00016A020 |
0.411 |
|
1991 |
Marshall JA, Wang XJ. Highly diastereoselective SE' additions of enantioenriched allenylstannanes to (S)-2-(benzyloxy)propanal Journal of Organic Chemistry. 56: 3211-3213. DOI: 10.1021/Jo00010A007 |
0.385 |
|
1991 |
Marshall JA, Blough BE. Diastereodifferentiation in SN2' additions of methylcuprates to nonracemic acyclic vinyloxiranes The Journal of Organic Chemistry. 56: 2225-2234. DOI: 10.1021/Jo00006A049 |
0.338 |
|
1991 |
Marshall JA, Wang XJ. Synthesis of furans by silver(I)-promoted cyclization of allenyl ketones and aldehydes The Journal of Organic Chemistry. 56: 960-969. DOI: 10.1021/Jo00003A013 |
0.416 |
|
1991 |
Marshall JA, Luke GP. Diastereoselective additions of enantioenriched .gamma.-(alkoxy)allyl stannanes to .alpha.-alkoxy aldehydes: a synthetic route to carbohydrates Journal of Organic Chemistry. 56: 483-485. DOI: 10.1021/Jo00002A001 |
0.359 |
|
1991 |
Marshall JA, Welmaker GS, Gung BW. On The 1,3-Isomerization Of Nonracemic Alpha -(Alkoxy)Allyl Stannanes Journal of the American Chemical Society. 113: 647-656. DOI: 10.1021/Ja00002A038 |
0.392 |
|
1990 |
Marshall JA, Wang XJ. Diastereoselective Additions Of Allenylstannanes To Aldehydes Journal of Organic Chemistry. 55: 6246-6248. DOI: 10.1021/Jo00313A007 |
0.392 |
|
1990 |
Marshall JA, Wang XJ. [2,3]-Wittig rearrangement of nonracemic (propargyloxy)acetic acids and esters. Synthesis of optically active 2,5-dihydrofurans The Journal of Organic Chemistry. 55: 2995-2996. DOI: 10.1021/Jo00297A004 |
0.397 |
|
1990 |
Marshall JA, Salovich JM, Shearer BG. Stereoselective synthesis of a nonracemic hydronaphthalene subunit of kijanolide Journal of Organic Chemistry. 55: 2398-2403. DOI: 10.1021/Jo00295A030 |
0.365 |
|
1990 |
Marshall JA, Blough BE. Synthesis of polypropionate subunits by SN2' addition of cuprates to nonracemic acyclic vinyloxiranes The Journal of Organic Chemistry. 55: 1540-1547. DOI: 10.1021/Jo00292A031 |
0.441 |
|
1990 |
Wu YD, Houk KN, Marshall JA. Transition structure for the [2,3]-Wittig rearrangement and analysis of stereoselectivities The Journal of Organic Chemistry. 55: 1421-1423. DOI: 10.1021/Jo00292A007 |
0.32 |
|
1990 |
Marshall JA, Robinson ED, Lebreton J. Synthesis of the tumor-inhibitory tobacco constituents .alpha.- and .beta.-2,7,11-cembratriene-4,6-diol by diastereoselective [2,3] Wittig ring contraction The Journal of Organic Chemistry. 55: 227-239. DOI: 10.1021/Jo00288A038 |
0.355 |
|
1990 |
MARSHALL JA, BLOUGH BE. ChemInform Abstract: Synthesis of Polypropionate Subunits by SN2′ Addition of Cuprates to Nonracemic Acyclic Vinyloxiranes. Cheminform. 21. DOI: 10.1002/chin.199032098 |
0.316 |
|
1989 |
Marshall JA. SN2' Additions of organocopper reagents to vinyloxiranes Chemical Reviews. 89: 1503-1511. DOI: 10.1021/Cr00097A006 |
0.339 |
|
1988 |
Marshall JA, Lebreton J. [2,3] Wittig ring contraction: synthesis of p-menthane derivatives Journal of Organic Chemistry. 53: 4108-4112. DOI: 10.1021/Jo00252A044 |
0.343 |
|
1988 |
Marshall JA, Crooks SL, DeHoff BS. Cembranolide total synthesis. Macrocyclization of (.alpha.-alkoxyallyl)stannane-acetylenic aldehydes as a route to cembrane lactones Journal of Organic Chemistry. 53: 1616-1623. DOI: 10.1021/Jo00243A005 |
0.42 |
|
1988 |
Marshall JA, Lebreton J. Enantioselective synthesis of macrocyclic propargylic alcohols by [2,3] Wittig ring contraction. Synthesis of (+)-aristolactone and cembranoid precursors Journal of the American Chemical Society. 110: 2925-2931. DOI: 10.1021/Ja00217A039 |
0.44 |
|
1987 |
Marshall JA, Andrews RC, Lebioda L. Synthetic studies on cembranolides. Stereoselective total synthesis of isolobophytolide The Journal of Organic Chemistry. 52: 2378-2388. DOI: 10.1021/Jo00388A008 |
0.458 |
|
1987 |
Marshall JA, Shearer BG, Crooks SL. Thermal and catalyzed intramolecular Diels-Alder cyclizations of 2,8,10-undecatrienals Journal of Organic Chemistry. 52: 1236-1245. DOI: 10.1021/Jo00383A012 |
0.323 |
|
1987 |
Marshall JA, Jenson TM, DeHoff BS. Synthesis of cembrane natural products via [2,3] Wittig ring contraction of propargylic ethers Journal of Organic Chemistry. 52: 3860-3866. DOI: 10.1021/Jo00226A026 |
0.392 |
|
1987 |
Marshall JA, Grote J, Audia JE. Acyclic stereocontrol in catalyzed intramolecular Diels-Alder cyclizations leading to octahydronaphthalenecarboxaldehydes Journal of the American Chemical Society. 109: 1186-1194. DOI: 10.1021/Ja00238A030 |
0.45 |
|
1987 |
Marshall JA, Lebreton J, DeHoff BS, Jenson TM. Total synthesis of the germacranolide (±)-aristolactone via [2,3] wittig ring contraction Tetrahedron Letters. 28: 723-726. DOI: 10.1016/S0040-4039(01)80972-2 |
0.379 |
|
1987 |
Marshall JA, DeHoff BS, Crooks SL. Stereoselective synthesis of cembranolide precursors via macrocyclization of α-alkoxyallylstannane aldehydes Tetrahedron Letters. 28: 527-530. DOI: 10.1016/S0040-4039(00)95773-3 |
0.438 |
|
1986 |
Andrews RC, Marshall JA, Dehoff BS. A Convenient Two-Step Procedure for Lactone α-Methylenation Synthetic Communications. 16: 1593-1598. DOI: 10.1080/00397918608056413 |
0.326 |
|
1986 |
Marshall J, Audia J, Grote J. Additions and Corrections - Acyclic Stereocontrol in Catalyzed Intramolecular Diels-Alder Cyclizations of 4-Methyl-2,8,10-undecatrienals. Journal of Organic Chemistry. 51: 4326-4326. DOI: 10.1021/Jo00372A613 |
0.4 |
|
1986 |
Marshall JA, Jenson TM, DeHoff BS. [2,3]-Wittig ring contraction. A new route to cembranoid natural products Journal of Organic Chemistry. 51: 4316-4319. DOI: 10.1021/Jo00372A048 |
0.316 |
|
1986 |
Marshall JA, Grote J, Shearer B. A stereoselective synthesis of the hydronaphthalene substructure of kijanolide Journal of Organic Chemistry. 51: 1633-1635. DOI: 10.1021/Jo00359A060 |
0.308 |
|
1986 |
Marshall JA, DeHoff BS. The synthesis of cembranolide precursors via addition of allylstannanes to conjugated aldehydes Journal of Organic Chemistry. 51: 863-872. DOI: 10.1021/Jo00356A022 |
0.476 |
|
1986 |
Marshall JA, Cleary DG. Synthesis of 7(8)-desoxyasperdiol. A precursor of the cembranoid asperdiol Journal of Organic Chemistry. 51: 858-863. DOI: 10.1021/Jo00356A021 |
0.445 |
|
1986 |
Marshall JA, Audia JE, Grote J. Acyclic Stereocontrol in Catalyzed Intramolecular Diels-Alder Cyclizations of 4-Methyl-2,8,10-undecatrienals. Cheminform. 17. DOI: 10.1002/Chin.198639120 |
0.397 |
|
1986 |
MARSHALL JA, CLEARY DG. ChemInform Abstract: Synthesis of 7(8)-Desoxyasperdiol (I). A Precursor of the Cembranoid Asperdiol. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198634316 |
0.338 |
|
1986 |
Marshall JA, Dehoff BS. The Synthesis of Cembranolide Precursors via Addition of Allylstannanes to Conjugated Aldehydes. Cheminform. 17. DOI: 10.1002/Chin.198634315 |
0.476 |
|
1985 |
MARSHALL JA, AUDIA VH. ChemInform Abstract: ADDITION OF N-BUTYLCUPRATES TO α-METHYLENECYCLOALKYLIDENE EPOXIDES Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198541159 |
0.303 |
|
1985 |
Marshall JA, Andrews RC. Coupling of allylic alcohol epoxides with sulfur-stabilized allylic anions The Journal of Organic Chemistry. 50: 1602-1606. DOI: 10.1002/Chin.198537203 |
0.325 |
|
1985 |
Marshall JA, Audia JE, Grote J. Intramolecular Diels-Alder Cyclization Of Conjugated Aldehydes. Synthesis Of A Chlorothricolide Intermediate Cheminform. 16. DOI: 10.1002/Chin.198528142 |
0.491 |
|
1985 |
MARSHALL JA, PETERSON JC, LEBIODA L. ChemInform Abstract: SYNTHESIS OF TRIANNULANES VIA INTRAMOLECULAR (2 + 1) CYCLIZATIONS OF LARGE-RING CYCLOALKENES Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198503185 |
0.308 |
|
1984 |
Marshall JA, Audia JE, Grote J. Intramolecular Diels-Alder cyclization of conjugated aldehydes: synthesis of a chlorothricolide intermediate Journal of Organic Chemistry. 49: 5277-5279. DOI: 10.1021/Jo00200A062 |
0.491 |
|
1984 |
Marshall JA, Coghlan MJ, Watanabe M. Synthetic studies on cembranolides. Stereoselective synthesis of epoxy ester intermediates Journal of Organic Chemistry. 49: 747-753. DOI: 10.1021/Jo00179A003 |
0.494 |
|
1984 |
Marshall JA, Peterson JC, Lebioda L. Synthesis of triannulanes via intramolecular [2 + 1] cyclizations of large-ring cycloalkenes Journal of the American Chemical Society. 106: 6006-6015. DOI: 10.1021/Ja00332A044 |
0.31 |
|
1984 |
Marshall JA, Flynn KE. Synthesis Of (R)-(+)-(10.10)- And -(22.10)Betweenanene And Related Trans-Cyclodecenes Cheminform. 15. DOI: 10.1002/Chin.198419158 |
0.353 |
|
1983 |
Marshall JA, Flynn KE. A stereorational synthesis of optically active trans-cycloalkenes and [10.10]betweenanene Journal of the American Chemical Society. 105: 3360-3362. DOI: 10.1021/Ja00348A081 |
0.305 |
|
1983 |
Marshall JA, Conrow RE. Total synthesis of (.+-.)-spiniferin-1, a naturally occurring 1,6-methano[10]annulene Journal of the American Chemical Society. 105: 5679-5688. DOI: 10.1002/Chin.198348288 |
0.412 |
|
1982 |
Marshall JA, Karas LJ, Coghlan MJ. Interconversion of cembranolide .delta.- and .gamma.-lactones: synthesis of the C-1 epimer of isolobophytolide Journal of Organic Chemistry. 47: 699-701. DOI: 10.1021/Jo00343A019 |
0.38 |
|
1982 |
Marshall JA, Royce RD. Synthetic studies on cembranolides. Stereoselective synthesis of a crassin acetate synthon Journal of Organic Chemistry. 47: 693-698. DOI: 10.1021/Jo00343A018 |
0.479 |
|
1982 |
Marshall JA, Karas LJ, Coghlan MJ. Interconversion Of Cembranolide Δ- And Γ-Lactones: Synthesis Of The C-1 Epimer Of Isolobophytolide Cheminform. 13. DOI: 10.1002/Chin.198235289 |
0.405 |
|
1982 |
Marshall JA, Royce RDJ. Synthetic studies on cembranolides. Stereoselective synthesis of a crassin acetate synthon Cheminform. 13. DOI: 10.1002/Chin.198235189 |
0.479 |
|
1980 |
Marshall JA, Black TH. [20.10]-, [22.10]-, and [26.10]Betweenanenes, conformationally flexible bicyclic alkenes: synthesis, chemistry and optical resolution Journal of the American Chemical Society. 102: 7581-7583. DOI: 10.1021/Ja00545A040 |
0.329 |
|
1980 |
Marshall JA, Conrow RE. Total synthesis of (.+-.)-dihydrospiniferin-1: a furanosesquiterpene with a 1,6-methano[10]annulene carbon skeleton Journal of the American Chemical Society. 102: 4274-4275. DOI: 10.1021/Ja00532A056 |
0.32 |
|
1980 |
Marshall JA, Konicek TR, Flynn KE. Synthesis and absolute configuration of optically active trans-1,2-disubstituted cycloalkenes Journal of the American Chemical Society. 102: 3287-3288. DOI: 10.1021/Ja00529A085 |
0.327 |
|
1979 |
Marshall JA, Karas LJ, Royce RD. Reduction-elimination of some vicinal cycloalkyl cyanohydrin derivatives. Stereoselective synthesis of cycloalkenes The Journal of Organic Chemistry. 44: 2994-2999. DOI: 10.1021/Jo01331A009 |
0.472 |
|
1979 |
Marshall JA, Chung K. An abbreviated stereorational synthesis of [10.10] between anene Journal of Organic Chemistry. 44: 1566-1567. DOI: 10.1021/Jo01323A044 |
0.438 |
|
1979 |
Marshall JA, Flynn GA. Stereoselective synthesis of racemic elemanolide dilactones related to vernolepin Journal of Organic Chemistry. 10: 1391-1397. DOI: 10.1021/Jo01323A007 |
0.429 |
|
1979 |
Marshall JA, Chung K. An abbreviated stereorational synthesis of [10.10] between anene Cheminform. 10. DOI: 10.1002/Chin.197936184 |
0.438 |
|
1978 |
Marshall JA, Wuts PGM. Stereocontrolled total synthesis of .alpha.- and .beta.-santonin The Journal of Organic Chemistry. 43: 1086-1089. DOI: 10.1021/Jo00400A013 |
0.307 |
|
1978 |
Marshall JA, Karas LJ. Stereochemistry of vicinal cyanohydrin reduction-elimination Journal of the American Chemical Society. 100: 3615-3616. DOI: 10.1021/Ja00479A063 |
0.326 |
|
1978 |
Marshall JA, Wuts PGM. Stereorational total synthesis of the marine diterpene dictyolene and its C-11 epimer Journal of the American Chemical Society. 100: 1627-1629. DOI: 10.1021/Ja00473A063 |
0.395 |
|
1977 |
Marshall JA, Flynn GA. The 2-Chloro-2-propenyl Side Chain. A Useful Acetic Acid Equivalent Synthetic Communications. 7: 417-421. DOI: 10.1080/00397917708050774 |
0.4 |
|
1977 |
Marshall JA, Wuts PGM. The Synthesis of Hydronaphthalenes fromm-Toluic AcidviaCyclization of Thioacetal Monosulfoxides Synthetic Communications. 7: 233-237. DOI: 10.1080/00397917708050740 |
0.329 |
|
1977 |
Marshall JA, Bierenbaum R. Synthesis of olefins via reduction-decyanation of .beta.,.gamma.-unsaturated nitriles Journal of Organic Chemistry. 42: 3309-3311. DOI: 10.1021/Jo00440A029 |
0.321 |
|
1977 |
Marshall JA, Wuts PGM. Stereoselective synthesis of racemic occidentalol and related cis-fused hexahydronaphthalenes from m-toluic acid The Journal of Organic Chemistry. 42: 1794-1798. DOI: 10.1021/Jo00430A027 |
0.329 |
|
1977 |
Marshall JA, Lewellyn ME. Reduction-elimination of cyclic phosphate derivatives as a route to alkenes The Journal of Organic Chemistry. 42: 1311-1315. DOI: 10.1021/Jo00428A009 |
0.371 |
|
1976 |
Marshall JA, Ellison RH. Letter: The stereoselective total synthesis of pseudoguaianolides: confertin. Journal of the American Chemical Society. 98: 4312-3. PMID 932363 DOI: 10.1021/Ja00430A051 |
0.452 |
|
1976 |
MARSHALL JA, ELLISON RH. ChemInform Abstract: THE STEREOSELECTIVE TOTAL SYNTHESIS OF PSEUDOGUAIANOLIDES- CONFERTIN Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/Chin.197640347 |
0.458 |
|
1975 |
Marshall JA, Lewellyn ME. The Synthesis of Alkenes via Reduction-Elimination of 1,2-Diol Cyclic Phosphate Derivatives Synthetic Communications. 5: 293-297. DOI: 10.1080/00397917508064124 |
0.352 |
|
1975 |
Marshall JA, Ellison RH. Stereoselective synthesis of cycloalkene-fused butyrolactones via cyclopropylcarbinol solvolysis The Journal of Organic Chemistry. 40: 2070-2073. DOI: 10.1021/Jo00902A013 |
0.475 |
|
1975 |
Marshall JA, Snyder WR. Total synthesis of (+-)-4-deoxydamsin. Structure correlation of pseudoguaianolide sesquiterpenes The Journal of Organic Chemistry. 40: 1656-1659. DOI: 10.1021/Jo00899A037 |
0.329 |
|
1975 |
Marshall JA, Seitz DE. Cleavage-elimination of 2,3-decalindione monothioketals leading to vinylic ester and lactone prototypes of vernolepin The Journal of Organic Chemistry. 40: 534-536. DOI: 10.1021/Jo00892A045 |
0.376 |
|
1975 |
MARSHALL JA, ELLISON RH. ChemInform Abstract: A STEREOSELECTIVE SYNTHESIS OF CYCLOALKENE-FUSED BUTYROLACTONES VIA CYCLOPROPYLCARBINOL SOLVOLYSIS Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/chin.197542241 |
0.367 |
|
1975 |
MARSHALL JA, SEITZ DE. ChemInform Abstract: THE SYNTHESIS OF A VERNOLEPIN PROTOTYPE Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/chin.197513276 |
0.319 |
|
1974 |
Marshall JA, Brady SF, Andersen NH. The chemistry of spiro(4.5)decane sesquiterpenes. Fortschritte Der Chemie Organischer Naturstoffe = Progress in the Chemistry of Organic Natural Products. Progrã¨S Dans La Chimie Des Substances Organiques Naturelles. 31: 283-376. PMID 4609864 |
0.427 |
|
1974 |
Marshall JA, Seitz DE. The Synthesis of a Vernolepin Prototype Synthetic Communications. 4: 395-398. DOI: 10.1080/00397917408064101 |
0.316 |
|
1974 |
Marshall JA, Ruth JA. Synthesis of racemic globulol via solvolysis-cyclization of a 2,7-cyclodecadien-1-ol derivative The Journal of Organic Chemistry. 39: 1971-1973. DOI: 10.1021/Jo00927A050 |
0.478 |
|
1974 |
Marshall JA, Seitz DE. Synthesis of ι-1,3-dithianyl carboxylic acids via cleavage of cyclic α-diketone monothioketals The Journal of Organic Chemistry. 39: 1814-1816. DOI: 10.1021/Jo00927A005 |
0.387 |
|
1972 |
Marshall JA, Litsas SB. Reduction of .alpha.-substituted acetoacetate enolates with lithium aluminum hydride Journal of Organic Chemistry. 37: 1840-1842. DOI: 10.1021/Jo00976A043 |
0.322 |
|
1972 |
Marshall JA, Greene AE. Synthesis of (+-)-guaiol and (+-)-7-epiguaiol Journal of Organic Chemistry. 37: 982-985. DOI: 10.1021/Jo00972A013 |
0.437 |
|
1972 |
Marshall JA, Ruden RA. Addition of lithium dimethylcopper to cnjugated cyclopropyl enones The Journal of Organic Chemistry. 37: 659-664. DOI: 10.1021/Jo00969A029 |
0.332 |
|
1972 |
Marshall JA, Huffman WF, Ruth JA. Stereoselective synthesis of hydroazulenes from cyclodecadienols Journal of the American Chemical Society. 94: 4691-4696. DOI: 10.1021/ja00768a042 |
0.361 |
|
1971 |
MARSHALL JA. Diene Synthesis via Boronate Fragmentation Synthesis. 1971: 229-235. DOI: 10.1055/s-1971-21706 |
0.332 |
|
1971 |
Marshall JA, Ruden RA. Selective degradation of guaiol. Synthesis of 7-epiguaiol The Journal of Organic Chemistry. 36: 2569-2571. DOI: 10.1021/Jo00816A050 |
0.358 |
|
1971 |
Marshall JA, Greene AE. Synthesis studies relating to guaiane sesquiterpenes Journal of Organic Chemistry. 36: 2035-2042. DOI: 10.1021/Jo00814A001 |
0.382 |
|
1971 |
Marshall JA, Cohen GM. Stereoselective total synthesis of racemic fukinone Journal of Organic Chemistry. 36: 877-882. DOI: 10.1021/Jo00806A004 |
0.466 |
|
1971 |
Marshall JA, Ruden RA. Stereoselective total synthesis of racemic nootkatone The Journal of Organic Chemistry. 36: 594-596. DOI: 10.1021/Jo00803A023 |
0.467 |
|
1971 |
Marshall JA, Warne TM. Total synthesis of (+-)-isonootkatone. Stereochemical studies of the Robinson annelation reaction with 3-penten-2-one Journal of Organic Chemistry. 36: 178-183. DOI: 10.1021/Jo00800A035 |
0.402 |
|
1970 |
Marshall JA, Andersen NH, Schlicher JW. Synthesis of bicyclo[5.4.0]undecanones via olefin cyclization The Journal of Organic Chemistry. 35: 858-861. DOI: 10.1021/Jo00828A084 |
0.625 |
|
1970 |
Marshall JA, Andersen NH, Johnson PC. Stereoselective synthesis of hydroazulenes The Journal of Organic Chemistry. 35: 186-191. DOI: 10.1021/Jo00826A040 |
0.615 |
|
1970 |
Marshall JA, Faubl H. Synthesis and chemistry of bicyclo[3.3.1]non-1-ene Journal of the American Chemical Society. 92: 948-955. DOI: 10.1021/Ja00707A034 |
0.403 |
|
1970 |
Marshall JA, Ruden RA. The stereoselective total synthesis of racemic nootkatone Tetrahedron Letters. 11: 1239-1242. DOI: 10.1016/S0040-4039(01)91598-9 |
0.361 |
|
1970 |
MARSHALL JA, ANDERSEN NH, SCHLICHER JW. ChemInform Abstract: SYNTH. VON BICYCLO(5,4,0)UNDECANONEN UEBER EINE OLEFIN-CYCLISIERUNG Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197025247 |
0.521 |
|
1970 |
MARSHALL JA, ANDERSEN NH, JOHNSON PC. ChemInform Abstract: STEREOSELEKTIVE SYNTH. VON HYDROAZULENEN Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197021164 |
0.469 |
|
1969 |
Marshall JA, Babler JH. Heterolytic fragmentation of 1-substituted decahydroquinolines The Journal of Organic Chemistry. 34: 4186-4188. DOI: 10.1021/Jo01264A104 |
0.338 |
|
1968 |
Marshall JA, Partridge JJ. The Synthesis and stereochemistry of 5-substituted 2-methylcyclo-heptanones. The Journal of Organic Chemistry. 33: 4090-7. PMID 20560526 DOI: 10.1021/Jo01275A018 |
0.471 |
|
1968 |
Marshall JA, Babler JH. The stereochemistry of alkylboronate 1,3-elimination reactions Chemical Communications (London). 993-994. DOI: 10.1039/C19680000993 |
0.303 |
|
1968 |
Marshall JA, Bundy GL, Fanta WI. Studies relating to the synthesis of (+)-valeranone The Journal of Organic Chemistry. 33: 3913-3922. DOI: 10.1021/Jo01274A048 |
0.379 |
|
1968 |
Marshall JA, Hochstetler AR. Synthesis of (+-)-geosmin and the other 1,10-dimethyl-9-decalol isomers The Journal of Organic Chemistry. 33: 2593-2595. DOI: 10.1021/Jo01270A120 |
0.463 |
|
1968 |
Marshall JA, Pike MT. Stereoselective synthesis of .alpha.- and .beta.-agarofuran Journal of Organic Chemistry. 33: 435-437. DOI: 10.1021/Jo01265A096 |
0.319 |
|
1967 |
Marshall JA, Faubl H, Warne TM. The total synthesis of racemic isonootkatone (α-vetivone) Chemical Communications (London). 753-754. DOI: 10.1039/C19670000753 |
0.384 |
|
1967 |
Marshall JA, Scanio CJV, Iburg WJ. Synthesis of cyclodecenes from bicyclo[5.3.1]undecanediol derivatives Journal of Organic Chemistry. 32: 3750-3754. DOI: 10.1021/Jo01287A004 |
0.446 |
|
1967 |
Marshall JA, Andersen NH, Hochstetler AR. Reduction of malonic enolates with lithium aluminum hydride The Journal of Organic Chemistry. 32: 113-118. DOI: 10.1021/Jo01277A029 |
0.516 |
|
1967 |
Marshall JA, Wurth MJ. Stereochemistry of the photosensitized hydration of olefins Journal of the American Chemical Society. 89: 6788-6790. DOI: 10.1021/Ja01001A086 |
0.322 |
|
1967 |
Marshall JA, Andersen NH, Johnson PC. A stereoselective synthesis of hydroazulenes. Grounds for structure revision of the vetivane sesquiterpenes Journal of the American Chemical Society. 89: 2748-2750. DOI: 10.1021/Ja00987A050 |
0.545 |
|
1967 |
Marshall JA, Andersen NH. A synthesis of fused-ring cycloheptanols via cyclization of unsaturated aldehydes Tetrahedron Letters. 8: 1219-1222. DOI: 10.1016/S0040-4039(00)90671-3 |
0.329 |
|
1966 |
Church RF, Ireland RE, Marshall JA. Experiments directed toward the total synthesis of terpenes. VII. The synthesis of (+or-)-8-beta-carbomethoxy-13-oxopodocarpanone, a degradation product of phyllocladene. The Journal of Organic Chemistry. 31: 2526-30. PMID 5917441 DOI: 10.1021/Jo01346A023 |
0.694 |
|
1966 |
Marshall JA, Roebke H. Stereochemical Studies on 1,6 Additions to 10-Methyl-1(9),7-hexal-2-one by Grignard Reagents Journal of Organic Chemistry. 31: 3109-3113. DOI: 10.1021/Jo01348A009 |
0.305 |
|
1966 |
Marshall JA, Andersen NH. Synthesis of 4-Substituted 1,1-Dimethyl-trans-2-decalones via Conjugate Addition of Grignard Reagents The Journal of Organic Chemistry. 31: 667-673. DOI: 10.1021/Jo01341A006 |
0.626 |
|
1966 |
Marshall JA, Bundy GL. A New Fragmentation Reaction. The Synthesis of 1-Methyl-trans,trans-1,6-cyclodecadiene Journal of the American Chemical Society. 88: 4291-4292. DOI: 10.1021/Ja00970A053 |
0.403 |
|
1966 |
Marshall JA, Carroll RD. The Photochemically Initiated Addition of Alcohols to 1-Menthene. A New Type of Photochemical Addition to Olefins Journal of the American Chemical Society. 88: 4092-4093. DOI: 10.1021/Ja00969A037 |
0.303 |
|
1966 |
Marshall JA, Hochstetler AR. The stereoselective total synthesis of racemic telekin Tetrahedron Letters. 7: 55-58. DOI: 10.1016/S0040-4039(01)99629-7 |
0.361 |
|
1966 |
Johnson W, Marshall J, Keana J, Franck R, Martin D, Bauer J. Steroid total synthesis—hydrochrysene approach—XVI Tetrahedron. 22: 541-601. DOI: 10.1016/S0040-4020(01)90961-5 |
0.685 |
|
1965 |
MARSHALL JA, COHEN N, ARENSON KR. SYNTHESIS OF 4-DEMETHYLTETRAHYDROALANTOLACTONE. The Journal of Organic Chemistry. 30: 762-6. PMID 14285670 DOI: 10.1021/Jo01014A026 |
0.438 |
|
1965 |
Marshall JA, Schaeffer DJ. Synthesis of Bicyclo[4.4.0]decanones and Bicyclo[3.3.1]nonanones via the Wichterle Reaction Journal of Organic Chemistry. 30: 3642-3646. DOI: 10.1021/Jo01022A013 |
0.396 |
|
1965 |
Marshall JA, Cohen N. Synthesis of Fused-Ring α-Methylene-γ-butyrolactones The Journal of Organic Chemistry. 30: 3475-3480. DOI: 10.1021/Jo01021A047 |
0.383 |
|
1965 |
Marshall JA, Scanio CJV. Synthesis of Substituted cis-Cyclodecenes from Cyclooctanone Journal of Organic Chemistry. 30: 3019-3023. DOI: 10.1021/Jo01020A030 |
0.365 |
|
1965 |
Marshall JA, Andersen NH. 1(9)-Octal-2,7-dione The Journal of Organic Chemistry. 30: 1292-1294. DOI: 10.1021/Jo01015A536 |
0.329 |
|
1965 |
Marshall JA, Cohen N. The Stereoselective Total Synthesis of Alantolactone Journal of the American Chemical Society. 87: 2773-2774. DOI: 10.1021/Ja01090A055 |
0.456 |
|
1965 |
Marshall JA, Fanta WI, Bundy GL. The stereoselective synthesis of -valeranone Tetrahedron Letters. 6: 4807-4815. DOI: 10.1016/S0040-4039(01)89039-0 |
0.361 |
|
1964 |
Marshall JA, Fanta WI. The Synthesis of Bicyclic Ketols from Cyclohexanones The Journal of Organic Chemistry. 29: 2501-2505. DOI: 10.1021/Jo01032A004 |
0.456 |
|
1963 |
Marshall JA, Johnson WS. The Hydroborating Properties of Sodium Borohydride and Acetic Acid The Journal of Organic Chemistry. 28: 595-596. DOI: 10.1021/Jo01037A526 |
0.554 |
|
1963 |
Marshall JA, Johnson WS. Reduction of Steroidal Enamines The Journal of Organic Chemistry. 28: 421-423. DOI: 10.1021/Jo01037A035 |
0.575 |
|
1962 |
Ireland RE, Marshall JA. Experiments directed toward the total synthesis of terpenes. III. The use of trans-Δ6-octalone-1 in the preparation of dicyclic intermediates Journal of Organic Chemistry. 27: 1620-1627. DOI: 10.1021/Jo01052A032 |
0.709 |
|
1962 |
Ireland RE, Marshall JA. The n-butylthiomethylene blocking group Journal of Organic Chemistry. 27: 1615-1619. DOI: 10.1021/Jo01052A031 |
0.629 |
|
1962 |
Church RF, Ireland RE, Marshall JA. Experiments directed toward the total synthesis of terpenes. II. The synthesis of dl-6-keto-5,5,9-trimethyl-2-methylene-trans-decalyl-1α-acetic acid and derivatives Journal of Organic Chemistry. 27: 1118-1125. DOI: 10.1021/Jo01051A002 |
0.72 |
|
1962 |
Marshall JA, Johnson WS. Total Synthesis of Racemic Conessine Journal of the American Chemical Society. 84: 1485-1486. DOI: 10.1021/Ja00867A026 |
0.631 |
|
1961 |
Church RF, Ireland RE, Marshall JA. A novel approach to a key intermediate in the total synthesis of α-onocerin Tetrahedron Letters. 2: 34-38. DOI: 10.1016/S0040-4039(01)99201-9 |
0.68 |
|
1960 |
Church RF, Ireland RE, Marshall JA. The stereospecific total synthesis of d1-8β-carbomethoxy-13-oxopodocarpane, a degradation product of phyllocladene Tetrahedron Letters. 1: 1-4. DOI: 10.1016/S0040-4039(01)99337-2 |
0.651 |
|
1959 |
Ireland RE, Marshall JA. The n-butylthiomethylene grouping: A superior blocking group for the alkylation of ketones [12] Journal of the American Chemical Society. 81: 6336-6337. DOI: 10.1021/Ja01532A064 |
0.622 |
|
1959 |
Ireland RE, Marshall JA. A new synthetic method for the preparation of α-substituted β-ketoesters [4] Journal of the American Chemical Society. 81: 2907-2908. DOI: 10.1021/Ja01520A073 |
0.644 |
|
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