Year |
Citation |
Score |
2020 |
Wang Z, Martin SF. Total Syntheses of (±)-Melicolones A and B. Organic Letters. PMID 33136416 DOI: 10.1021/acs.orglett.0c03454 |
0.36 |
|
2020 |
Lepovitz LT, Martin SF. Biomimetically Inspired, One-Step Synthesis of Exotine A and Exotine B. The Journal of Organic Chemistry. PMID 32924509 DOI: 10.1021/Acs.Joc.0C01524 |
0.401 |
|
2020 |
Lepovitz LT, Meis AR, Thomas SM, Wiedeman J, Pham A, Mensa-Wilmot K, Martin SF. Design, Synthesis, and Evaluation of Novel Anti-Trypanosomal Compounds. Tetrahedron. 76. PMID 32382196 DOI: 10.1016/J.Tet.2020.131086 |
0.331 |
|
2020 |
Wypych RM, LaPlante SR, White PW, Martin SF. Structure-thermodynamics-relationships of hepatitis C viral NS3 protease inhibitors. European Journal of Medicinal Chemistry. 192: 112195. PMID 32151833 DOI: 10.1016/J.Ejmech.2020.112195 |
0.328 |
|
2020 |
Blumberg S, Martin SF. Racemic or enantioselective osmium-catalyzed dihydroxylation of olefins under near-neutral conditions Arkivoc. 2021: 7-14. DOI: 10.24820/Ark.5550190.P011.266 |
0.358 |
|
2020 |
Goodnough AM, Sahn JJ, Martin SF. Facile entry to substituted 2-arylpiperidines via an aza-Sakurai reaction Tetrahedron Letters. 61: 151777. DOI: 10.1016/J.Tetlet.2020.151777 |
0.488 |
|
2019 |
Wood MD, Klosowski DW, Martin SF. Stereoselective Total Synthesis of (±)-Alstoscholarisine E. Organic Letters. PMID 31789527 DOI: 10.1021/Acs.Orglett.9B04093 |
0.476 |
|
2019 |
Lepovitz LT, Martin SF. Diversity-Oriented Synthesis of Bioactive Azaspirocycles Tetrahedron. 75: 130637. DOI: 10.1016/J.Tet.2019.130637 |
0.477 |
|
2018 |
Lepovitz LT, Martin SF. Biomimetically Inspired Synthesis of Exotine A. Organic Letters. PMID 30525687 DOI: 10.1021/Acs.Orglett.8B03423 |
0.464 |
|
2018 |
Klosowski DW, Hethcox JC, Paull DH, Fang C, Donald JR, Shugrue CR, Pansick AD, Martin SF. Enantioselective Halolactonization Reactions using BINOL-derived Bifunctional Catalysts: Methodology, Diversification, and Applications. The Journal of Organic Chemistry. PMID 29717607 DOI: 10.1021/Acs.Joc.8B00490 |
0.481 |
|
2018 |
Linkens K, Schmidt HR, Sahn JJ, Kruse AC, Martin SF. Investigating isoindoline, tetrahydroisoquinoline, and tetrahydrobenzazepine scaffolds for their sigma receptor binding properties. European Journal of Medicinal Chemistry. 151: 557-567. PMID 29656199 DOI: 10.1016/J.Ejmech.2018.02.024 |
0.33 |
|
2018 |
Klosowski DW, Martin SF. Correction to "Synthesis of (+)-Disparlure via Enantioselective Iodolactonization". Organic Letters. PMID 29637784 DOI: 10.1021/Acs.Orglett.8B00999 |
0.433 |
|
2018 |
Klosowski DW, Martin SF. Synthesis of (+)-Disparlure via Enantioselective Iodolactonization. Organic Letters. PMID 29431447 DOI: 10.1021/Acs.Orglett.7B03911 |
0.466 |
|
2018 |
Martin S, Klosowski D. Enantioselective Synthesis of F-Ring Fragments of Kibdelone C via Desymmetrizing Bromolactonization of 1,4-Dihydrobenzoic Acid Synlett. 29: 430-432. DOI: 10.1055/S-0036-1591890 |
0.4 |
|
2018 |
Blumberg S, Martin SF. Toward the total synthesis of citreamicin η: Synthesis of the pentacyclic core and GAB-ring annelation model studies Tetrahedron. 74: 4981-4993. DOI: 10.1016/J.Tet.2018.04.049 |
0.464 |
|
2018 |
Hodges TR, Benjamin NM, Martin SF. Concise approach to the syntheses of (±)-gliocladin C and related diketopiperazine alkaloids Tetrahedron. 74: 3329-3338. DOI: 10.1016/J.Tet.2018.04.001 |
0.339 |
|
2017 |
Martin SF. Natural Products and Their Mimics as Targets of Opportunity for Discovery. The Journal of Organic Chemistry. PMID 28738152 DOI: 10.1021/Acs.Joc.7B01368 |
0.303 |
|
2017 |
Sahn JJ, Hodges TR, Chan JZ, Martin SF. Norbenzomorphan Scaffold: Chemical Tool for Modulating Sigma Receptor-Subtype Selectivity. Acs Medicinal Chemistry Letters. 8: 455-460. PMID 28435536 DOI: 10.1021/Acsmedchemlett.7B00066 |
0.325 |
|
2017 |
Hodges TR, Benjamin NM, Martin SF. Syntheses of Gliocladin C and Related Alkaloids. Organic Letters. PMID 28413880 DOI: 10.1021/Acs.Orglett.7B00735 |
0.338 |
|
2017 |
Yu R, Chen X, Martin SF, Wang Z. Differentially Substituted Phosphines via Decarbonylation of Acylphosphines. Organic Letters. PMID 28357867 DOI: 10.1021/Acs.Orglett.7B00579 |
0.435 |
|
2017 |
Blumberg S, Martin SF. Synthesis of the Pentacyclic Core of Citreamicin η. Organic Letters. PMID 28177637 DOI: 10.1021/Acs.Orglett.6B03760 |
0.481 |
|
2016 |
Stoltz BM, Martin S. Tetrahedron Young Investigator Award ~ 2016 Tetrahedron. DOI: 10.1016/J.Tet.2016.04.026 |
0.367 |
|
2015 |
Cheng B, Sunderhaus JD, Martin SF. Applications of Ring Closing Metathesis. Total Synthesis of (±)-Pseudotabersonine. Tetrahedron. 71: 7323-7331. PMID 26300565 DOI: 10.1016/J.Tet.2015.04.082 |
0.437 |
|
2015 |
Hethcox JC, Shanahan CS, Martin SF. Diastereoselective addition of monoorganocuprates to a chiral fumarate: reaction development and synthesis of (-)-dihydroprotolichesterinic acid. Tetrahedron. 71: 6361-6368. PMID 26273115 DOI: 10.1016/J.Tet.2015.05.023 |
0.464 |
|
2015 |
Knueppel D, Yang J, Cheng B, Mans D, Martin SF. Total Synthesis of the Aglycone of IB-00208. Tetrahedron. 71: 5741-5757. PMID 26273110 DOI: 10.1016/J.Tet.2015.05.024 |
0.42 |
|
2015 |
Yang J, Knueppel D, Cheng B, Mans D, Martin SF. Approaches to polycyclic 1,4-dioxygenated xanthones. Application to total synthesis of the aglycone of IB-00208. Organic Letters. 17: 114-7. PMID 25513888 DOI: 10.1021/Ol503336T |
0.375 |
|
2015 |
Knueppel D, Yang J, Cheng B, Mans D, Martin SF. Total synthesis of the aglycone of IB-00208 Tetrahedron. DOI: 10.1016/j.tet.2015.05.024 |
0.313 |
|
2015 |
Hethcox JC, Shanahan CS, Martin SF. Diastereoselective addition of monoorganocuprates to a chiral fumarate: Reaction development and synthesis of (-)-dihydroprotolichesterinic acid Tetrahedron. DOI: 10.1016/j.tet.2015.05.023 |
0.354 |
|
2014 |
Hardy S, Martin SF. Multicomponent, Mannich-type assembly process for generating novel, biologically-active 2-arylpiperidines and derivatives. Tetrahedron. 70: 7142-7157. PMID 25267860 DOI: 10.1016/J.Tet.2014.06.045 |
0.419 |
|
2014 |
Bian Z, Marvin CC, Pettersson M, Martin SF. Enantioselective total syntheses of citrinadins a and B. Stereochemical revision of their assigned structures. Journal of the American Chemical Society. 136: 14184-92. PMID 25211501 DOI: 10.1021/Ja5074646 |
0.831 |
|
2014 |
Sahn JJ, Granger BA, Martin SF. Evolution of a strategy for preparing bioactive small molecules by sequential multicomponent assembly processes, cyclizations, and diversification. Organic & Biomolecular Chemistry. 12: 7659-72. PMID 25135846 DOI: 10.1039/C4Ob00835A |
0.818 |
|
2014 |
Granger BA, Jewett IT, Butler JD, Martin SF. Concise total synthesis of (±)-actinophyllic acid. Tetrahedron. 70: 4094-4104. PMID 24882888 DOI: 10.1016/J.Tet.2014.03.034 |
0.814 |
|
2014 |
Myslinski JM, Clements JH, Martin SF. Protein-ligand interactions: probing the energetics of a putative cation-π interaction. Bioorganic & Medicinal Chemistry Letters. 24: 3164-7. PMID 24856058 DOI: 10.1016/J.Bmcl.2014.04.114 |
0.315 |
|
2014 |
Granger BA, Jewett IT, Butler JD, Martin SF. ChemInform Abstract: Concise Total Synthesis of (.+-.)-Actinophyllic Acid. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201445223 |
0.81 |
|
2013 |
Myslinski JM, Clements JH, Delorbe JE, Martin SF. Protein-Ligand Interactions: Thermodynamic Effects Associated with Increasing the Length of an Alkyl Chain. Acs Medicinal Chemistry Letters. 4. PMID 24349642 DOI: 10.1021/Ml400211Q |
0.313 |
|
2013 |
Shanahan CS, Fang C, Paull DH, Martin SF. Asymmetric Formal Total Synthesis of the Stemofoline Alkaloids: The Evolution, Development and Application of a Catalytic Dipolar Cycloaddition Cascade. Tetrahedron. 69: 7592-7607. PMID 24072939 DOI: 10.1016/J.Tet.2013.03.104 |
0.511 |
|
2013 |
Fu TH, McElroy WT, Shamszad M, Heidebrecht RW, Gulledge B, Martin SF. Studies toward welwitindolinones: formal syntheses of N-methylwelwitindolinone C isothiocyanate and related natural products. Tetrahedron. 69: 5588-5603. PMID 23976796 DOI: 10.1016/J.Tet.2013.03.010 |
0.83 |
|
2013 |
Granger BA, Jewett IT, Butler JD, Hua B, Knezevic CE, Parkinson EI, Hergenrother PJ, Martin SF. Synthesis of (±)-actinophyllic acid and analogs: applications of cascade reactions and diverted total synthesis. Journal of the American Chemical Society. 135: 12984-6. PMID 23972114 DOI: 10.1021/Ja4070206 |
0.818 |
|
2013 |
Bian Z, Marvin CC, Martin SF. Enantioselective total synthesis of (-)-citrinadin A and revision of its stereochemical structure. Journal of the American Chemical Society. 135: 10886-9. PMID 23837457 DOI: 10.1021/Ja405547F |
0.751 |
|
2013 |
Granger BA, Wang Z, Kaneda K, Fang Z, Martin SF. Multicomponent assembly processes for the synthesis of diverse yohimbine and corynanthe alkaloid analogues. Acs Combinatorial Science. 15: 379-86. PMID 23697376 DOI: 10.1021/Co400055B |
0.816 |
|
2013 |
Hethcox JC, Shanahan CS, Martin SF. Total synthesis of (-)-dihydroprotolichesterenic acid via diastereoselective conjugate addition to chiral fumarates. Tetrahedron Letters. 54: 2074-2076. PMID 23539490 DOI: 10.1016/J.Tetlet.2013.02.014 |
0.485 |
|
2013 |
Martin SF. Strategies for the Synthesis of Alkaloids and Novel Nitrogen Heterocycles Advances in Heterocyclic Chemistry. 110: 73-117. DOI: 10.1016/B978-0-12-408100-0.00003-3 |
0.337 |
|
2012 |
Fang C, Paull DH, Hethcox JC, Shugrue CR, Martin SF. Enantioselective iodolactonization of disubstituted olefinic acids using a bifunctional catalyst. Organic Letters. 14: 6290-3. PMID 23199100 DOI: 10.1021/Ol3030555 |
0.39 |
|
2012 |
Fang C, Shanahan CS, Paull DH, Martin SF. Enantioselective formal total syntheses of didehydrostemofoline and isodidehydrostemofoline through a catalytic dipolar cycloaddition cascade. Angewandte Chemie (International Ed. in English). 51: 10596-9. PMID 22987285 DOI: 10.1002/Anie.201205274 |
0.496 |
|
2012 |
Nichols AL, Zhang P, Martin SF. Concise Approach to 1,4-Dioxygenated Xanthones via Novel Application of the Moore Rearrangement. Tetrahedron. 68: 7591-7597. PMID 22962501 DOI: 10.1016/J.Tet.2012.05.094 |
0.47 |
|
2012 |
Sahn JJ, Martin SF. Expedient synthesis of norbenzomorphan library via multicomponent assembly process coupled with ring-closing reactions. Acs Combinatorial Science. 14: 496-502. PMID 22857149 DOI: 10.1021/Co300068A |
0.458 |
|
2012 |
Fu TH, McElroy WT, Shamszad M, Martin SF. Formal syntheses of naturally occurring welwitindolinones. Organic Letters. 14: 3834-7. PMID 22830424 DOI: 10.1021/Ol301424H |
0.809 |
|
2012 |
Paull DH, Fang C, Donald JR, Pansick AD, Martin SF. Bifunctional catalyst promotes highly enantioselective bromolactonizations to generate stereogenic C-Br bonds. Journal of the American Chemical Society. 134: 11128-31. PMID 22726214 DOI: 10.1021/Ja305117M |
0.389 |
|
2012 |
Wang Z, Kaneda K, Fang Z, Martin SF. Diversity Oriented Synthesis: Concise Entry to Novel Derivatives of Yohimbine and Corynanthe Alkaloids. Tetrahedron Letters. 53: 477-479. PMID 22544982 DOI: 10.1016/J.Tetlet.2011.10.115 |
0.443 |
|
2012 |
Donald JR, Granger BA, Hardy S, Sahn JJ, Martin SF. APPLICATIONS OF MULTICOMPONENT ASSEMBLY PROCESSES TO THE FACILE SYNTHESES OF DIVERSELY FUNCTIONALIZED NITROGEN HETEROCYCLES. Heterocycles. 84: 1089-1112. PMID 22451742 DOI: 10.3987/COM-11-S(P)92 |
0.815 |
|
2012 |
Donald JR, Wood RR, Martin SF. Application of a sequential multicomponent assembly process/huisgen cycloaddition strategy to the preparation of libraries of 1,2,3-triazole-fused 1,4-benzodiazepines. Acs Combinatorial Science. 14: 135-43. PMID 22273436 DOI: 10.1021/Co2002087 |
0.449 |
|
2012 |
Shi Y, Zhu CZ, Martin SF, Ren P. Probing the effect of conformational constraint on phosphorylated ligand binding to an SH2 domain using polarizable force field simulations. The Journal of Physical Chemistry. B. 116: 1716-27. PMID 22214214 DOI: 10.1021/Jp210265D |
0.309 |
|
2012 |
Granger BA, Kaneda K, Martin SF. Libraries of 2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinolin-2-amine derivatives via a multicomponent assembly process/1,3-dipolar cycloaddition strategy. Acs Combinatorial Science. 14: 75-9. PMID 22040015 DOI: 10.1021/Co2001636 |
0.795 |
|
2012 |
Dwyer MP, Martin SF. Synthesis of cyclopropane-containing leu-enkephalin analogs. Methods in Molecular Medicine. 23: 407-16. PMID 21380910 DOI: 10.1385/0-89603-517-4:407 |
0.392 |
|
2012 |
Hillier MC, Martin SF. A Conformationally Restricted β-Strand HIV Protease Inhibitor. Methods in Molecular Medicine. 23: 397-406. PMID 21380909 DOI: 10.1385/0-89603-517-4:397 |
0.301 |
|
2012 |
Wang Z, Kaneda K, Fang Z, Martin SF. Corrigendum to “Diversity oriented synthesis: concise entry to novel derivatives of Yohimbine and Corynanthe alkaloids” [Tetrahedron Lett. 53 (2011) 477–479] Tetrahedron Letters. 53: 1678. DOI: 10.1016/J.Tetlet.2012.01.100 |
0.421 |
|
2011 |
Sahn JJ, Martin SF. Facile Syntheses of Substituted, Conformationally-Constrained Benzoxazocines and Benzazocines via Sequential Multicomponent Assembly and Cyclization. Tetrahedron Letters. 52: 6855-6858. PMID 22711939 DOI: 10.1016/J.Tetlet.2011.10.022 |
0.469 |
|
2011 |
Knueppel D, Martin SF. Tandem Electrocyclic Ring Opening/Radical Cyclization: Application to the Total Synthesis of Cribrostatin 6. Tetrahedron. 67: 9765-9770. PMID 22125344 DOI: 10.1016/J.Tet.2011.08.064 |
0.462 |
|
2011 |
Myslinski JM, DeLorbe JE, Clements JH, Martin SF. Protein-ligand interactions: thermodynamic effects associated with increasing nonpolar surface area. Journal of the American Chemical Society. 133: 18518-21. PMID 22007755 DOI: 10.1021/Ja2068752 |
0.348 |
|
2011 |
Orr ST, Tian J, Niggemann M, Martin SF. Novel approach to the lundurine alkaloids: synthesis of the tetracyclic core. Organic Letters. 13: 5104-7. PMID 21888327 DOI: 10.1021/Ol201980R |
0.404 |
|
2011 |
Shanahan CS, Fuller NO, Ludolph B, Martin SF. Toward a total synthesis of the stemofoline alkaloids: Advancement of a 1,3-dipolar cycloaddition strategy. Tetrahedron Letters. 52: 4076-4079. PMID 21857754 DOI: 10.1016/J.Tetlet.2011.05.121 |
0.476 |
|
2011 |
Granger BA, Kaneda K, Martin SF. Multicomponent assembly strategies for the synthesis of diverse tetrahydroisoquinoline scaffolds. Organic Letters. 13: 4542-5. PMID 21834504 DOI: 10.1021/Ol201739U |
0.821 |
|
2011 |
Nichols AL, Zhang P, Martin SF. General and expedient synthesis of 1,4-dioxygenated xanthones. Organic Letters. 13: 4696-9. PMID 21812455 DOI: 10.1021/Ol201910V |
0.467 |
|
2011 |
O'Keefe BM, Mans DM, Kaelin DE, Martin SF. Studies Toward the Syntheses of Pluramycin Natural Products. The First Total Synthesis of Isokidamycin. Tetrahedron. 67: 6524-6538. PMID 21804649 DOI: 10.1016/J.Tet.2011.05.117 |
0.808 |
|
2011 |
O'Keefe BM, Simmons N, Martin SF. Facile Access to Sterically Hindered Aryl Ketones via Carbonylative Cross-Coupling: Application to the Total Synthesis of Luteolin. Tetrahedron. 67: 4344-4351. PMID 21712966 DOI: 10.1016/J.Tet.2011.03.074 |
0.409 |
|
2011 |
Hardy S, Martin SF. Multicomponent assembly and diversification of novel heterocyclic scaffolds derived from 2-arylpiperidines. Organic Letters. 13: 3102-5. PMID 21598984 DOI: 10.1021/Ol201010S |
0.423 |
|
2011 |
Dietz J, Martin SF. Novel Entry to the Tricyclic Core of Stemofoline and Didehydrostemofoline. Tetrahedron Letters. 52: 2048-2050. PMID 21516222 DOI: 10.1016/J.Tetlet.2010.10.038 |
0.36 |
|
2011 |
Sahn JJ, Su JY, Martin SF. Facile and unified approach to skeletally diverse, privileged scaffolds. Organic Letters. 13: 2590-3. PMID 21513290 DOI: 10.1021/Ol200709H |
0.411 |
|
2011 |
Donald JR, Martin SF. Synthesis and diversification of 1,2,3-triazole-fused 1,4-benzodiazepine scaffolds. Organic Letters. 13: 852-5. PMID 21275426 DOI: 10.1021/Ol1028404 |
0.439 |
|
2011 |
Benjamin NM, Martin SF. Enantioselective synthesis of 2,2,5-tri- and 2,2,5,5-tetrasubstituted tetrahydrofurans via [4 + 2] cycloaddition and ring-opening cross-metathesis. Organic Letters. 13: 450-3. PMID 21210696 DOI: 10.1021/Ol102798F |
0.475 |
|
2011 |
Martin SF. Reprint of: Organic synthesis - 2011: Perspective, journeys, and accounts Tetrahedron. 67: 10067. DOI: 10.1016/J.Tet.2011.11.011 |
0.324 |
|
2010 |
Delorbe JE, Clements JH, Whiddon BB, Martin SF. Thermodynamic and Structural Effects of Macrocyclization as a Constraining Method in Protein-Ligand Interactions. Acs Medicinal Chemistry Letters. 1: 448-452. PMID 21116482 DOI: 10.1021/Ml100142Y |
0.318 |
|
2010 |
Procko KJ, Li H, Martin SF. Approach toward the total synthesis of 5-hydroxyaloin A. Organic Letters. 12: 5632-5. PMID 21082813 DOI: 10.1021/Ol102318K |
0.481 |
|
2010 |
O'Keefe BM, Mans DM, Kaelin DE, Martin SF. Total synthesis of isokidamycin. Journal of the American Chemical Society. 132: 15528-30. PMID 20958036 DOI: 10.1055/S-0030-1259214 |
0.797 |
|
2010 |
Clements JH, DeLorbe JE, Benfield AP, Martin SF. Binding of flexible and constrained ligands to the Grb2 SH2 domain: structural effects of ligand preorganization. Acta Crystallographica. Section D, Biological Crystallography. 66: 1101-15. PMID 20944243 DOI: 10.1107/S0907444910035584 |
0.779 |
|
2010 |
Cheng B, Sunderhaus JD, Martin SF. Concise total synthesis of (+/-)-pseudotabersonine via double ring-closing metathesis strategy. Organic Letters. 12: 3622-5. PMID 20704405 DOI: 10.1021/Ol101356U |
0.502 |
|
2010 |
Deck JA, Martin SF. Enantioselective synthesis of (+)-isolysergol via ring-closing metathesis. Organic Letters. 12: 2610-3. PMID 20462232 DOI: 10.1021/Ol100819F |
0.827 |
|
2010 |
Heidebrecht RW, Gulledge B, Martin SF. Approaches to N-methylwelwitindolinone C isothiocyanate: facile synthesis of the tetracyclic core. Organic Letters. 12: 2492-5. PMID 20446675 DOI: 10.1021/Ol1006373 |
0.437 |
|
2010 |
DeLorbe JE, Lotz MD, Martin SF. Concise total synthesis of (+/-)-lycopladine A. Organic Letters. 12: 1576-9. PMID 20196615 DOI: 10.1021/Ol100273P |
0.495 |
|
2010 |
Cheng B, Sunderhaus JD, Martin SF. ChemInform Abstract: Concise Total Synthesis of (.+-.)-Pseudotabersonine via Double Ring-Closing Metathesis Strategy. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201050193 |
0.351 |
|
2010 |
DeLorbe JE, Lotz MD, Martin SF. ChemInform Abstract: Concise Total Synthesis of (.+-.)-Lycopladine A (I). Cheminform. 41: no-no. DOI: 10.1002/CHIN.201032202 |
0.327 |
|
2010 |
Reichelt A, Bur SK, Martin SF. ChemInform Abstract: Applications of Vinylogous Mannich Reactions. Total Synthesis of the Angiotensin Converting Enzyme Inhibitor (-)-A58365A. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200250181 |
0.608 |
|
2010 |
Neipp CE, Martin SF. ChemInform Abstract: A Ring-Closing Olefin Metathesis Approach to Bridged Azabicyclic Structures. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200227188 |
0.797 |
|
2010 |
Bur SK, Martin SF. ChemInform Abstract: Vinylogous Mannich Reactions: Selectivity and Synthetic Utility Cheminform. 32: no-no. DOI: 10.1002/CHIN.200129218 |
0.732 |
|
2010 |
Dwyer MP, Martin SF. ChemInform Abstract: Synthesis of Cyclopropane-Containing Leu-Enkephalin Analogues Cheminform. 31: no-no. DOI: 10.1002/CHIN.200030264 |
0.352 |
|
2010 |
Martin SF, Barr KJ, Smith DW, Bur SK. ChemInform Abstract: Applications of Vinylogous Mannich Reactions. Concise Enantiospecific Total Syntheses of (+)-Croomine. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199951209 |
0.741 |
|
2010 |
Martin SF, Hom RK, Dwyer MP. ChemInform Abstract: Synthesis of Enantiomerically Pure Vinylcyclopropanes by SN2′ Allylic Carboxylate Displacements. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199947047 |
0.37 |
|
2010 |
Martin SF, Bur SK. ChemInform Abstract: Vinylogous Mannich Reactions. Stereoselective Formal Synthesis of Pumiliotoxin 251D. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199946203 |
0.746 |
|
2010 |
Martin SF, Chen KX, Todd Eary C. ChemInform Abstract: An Enantioselective Total Synthesis of (+)-Geissoschizine. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199942233 |
0.349 |
|
2010 |
MARTIN SF, DWYER MP. ChemInform Abstract: Iodocyclopropanes as Versatile Intermediates for the Synthesis of Substituted Cyclopropanes. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199822067 |
0.394 |
|
2010 |
MARTIN SF, BUR SK. ChemInform Abstract: The Stereochemical Course of Intramolecular Vinylogous Mannich Reactions. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199809125 |
0.732 |
|
2010 |
MARTIN SF, CHEN H, COURTNEY AK, LIAO Y, PAETZEL M, RAMSER MN, WAGMAN AS. ChemInform Abstract: Ring-Closing Olefin Metathesis for the Synthesis of Fused Nitrogen Heterocycles. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199638068 |
0.366 |
|
2010 |
MARTIN SF, BARR KJ. ChemInform Abstract: Vinylogous Mannich Reactions. The Asymmetric Total Synthesis of (+)- Croomine. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199630282 |
0.369 |
|
2010 |
DOYLE MP, DYATKIN AB, KALININ AV, RUPPAR DA, MARTIN SF, SPALLER MR, LIRAS S. ChemInform Abstract: Highly Selective Enantiomer Differentiation in Intramolecular Cyclopropanation Reactions of Racemic Secondary Allylic Diazoacetates. Cheminform. 27: no-no. DOI: 10.1002/chin.199611038 |
0.302 |
|
2010 |
MARTIN SF, CLARK CW, CORBETT JW. ChemInform Abstract: Applications of Vinylogous Mannich Reactions. Asymmetric Synthesis of the Heteroyohimboid Alkaloids (-)-Ajmalicine (VII), (+)-19-epi- Ajmalicine (XIV), and (-)-Tetrahydroalstonine (XV). Cheminform. 26: no-no. DOI: 10.1002/CHIN.199539244 |
0.362 |
|
2010 |
MARTIN SF, LIAO Y, CHEN H, PAETZEL M, RAMSER MN. ChemInform Abstract: Novel Route to Fused Nitrogen Heterocycles by Olefin Metathesis. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199501174 |
0.31 |
|
2010 |
MARTIN SF, SPALLER MR, LIRAS S, HARTMANN B. ChemInform Abstract: Enantio- and Diastereoselectivity in the Intramolecular Cyclopropanation of Secondary Allylic Diazoacetates. Cheminform. 25: no-no. DOI: 10.1002/chin.199440067 |
0.326 |
|
2010 |
MARTIN SF, LIAO Y, WONG Y, REIN T. ChemInform Abstract: A Novel Approach to the Asymmetric Synthesis of Manzamine A (VII). Construction of the Tetracyclic ABCE Ring System (VI). Cheminform. 25: no-no. DOI: 10.1002/CHIN.199424256 |
0.329 |
|
2010 |
MARTIN SF, LIRAS S. ChemInform Abstract: Novel Applications of Vinylogous Mannich Reactions. Total Synthesis of Rugulovasines A and B. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199407261 |
0.316 |
|
2010 |
MARTIN SF, OALMANN CJ, LIRAS S. ChemInform Abstract: Enantioselective, Rhodium-Catalyzed Intramolecular Cyclopropanation of Homoallylic Diazo Acetates (III). Cheminform. 24: no-no. DOI: 10.1002/CHIN.199316098 |
0.33 |
|
2010 |
LYNCH VM, CORBETT JW, MARTIN SF, DAVIS BE. ChemInform Abstract: Structure of a Chiral Intermediate in the Synthesis of (+)-19- Epiajmalicine. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199305279 |
0.311 |
|
2010 |
MARTIN SF, AUSTIN RE, OALMANN CJ. ChemInform Abstract: Stereoselective Synthesis of 1,2,3-Trisubstituted Cyclopropanes as Novel Dipeptide Isosters. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199147193 |
0.375 |
|
2010 |
MARTIN SF, BENAGE B, GERACI LS, HUNTER JE, MORTIMORE M. ChemInform Abstract: Unified Strategy for Synthesis of Indole and 2-Oxindole Alkaloids. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199145279 |
0.332 |
|
2010 |
LYNCH VM, ZINKE PW, MARTIN SF, DAVIS BE. ChemInform Abstract: Structure of a Key Intermediate in the Asymmetric Synthesis of (+)-KDO. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199129265 |
0.331 |
|
2010 |
MARTIN SF, MORTIMORE M. ChemInform Abstract: New Methods for the Synthesis of Oxindole Alkaloids. Total Synthesis of Isopteropodine and Pteropodine. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199125249 |
0.306 |
|
2010 |
LYNCH VM, CORBETT JW, MARTIN SF, DAVIS BE. ChemInform Abstract: Structure of a Key Intermediate in the Synthesis of (-)-5- Carboxytetrahydroalstonine and (-)-Tetrahydroalstonine Cheminform. 22: no-no. DOI: 10.1002/CHIN.199120268 |
0.314 |
|
2010 |
LYNCH VM, LI W, MARTIN SF, DAVIS BE. ChemInform Abstract: The Structure of a Key Intermediate in the Total Synthesis of Dendrobine Cheminform. 22: no-no. DOI: 10.1002/CHIN.199120266 |
0.315 |
|
2009 |
Amorde SM, Jewett IT, Martin SF. Iminium Ion Cascade Reactions: Stereoselective Synthesis of Quinolizidines and Indolizidines. Tetrahedron. 65: 3222-3231. PMID 20890382 DOI: 10.1016/J.Tet.2008.10.074 |
0.824 |
|
2009 |
Sunderhaus JD, Dockendorff C, Martin SF. Synthesis of Diverse Heterocyclic Scaffolds via Tandem Additions to Imine Derivatives and Ring-Forming Reactions. Tetrahedron. 65: 6454-6469. PMID 20625454 DOI: 10.1016/J.Tet.2009.05.009 |
0.481 |
|
2009 |
Fu TH, Bonaparte A, Martin SF. Synthesis of β-Heteroaryl Propionates via Trapping of Carbocations with π-Nucleophiles. Tetrahedron Letters. 50: 3253-3257. PMID 20161309 DOI: 10.1016/J.Tetlet.2009.02.018 |
0.416 |
|
2009 |
Martin SF. Recent Applications of Imines as Key Intermediates in the Synthesis of Alkaloids and Novel Nitrogen Heterocycles. Pure and Applied Chemistry. Chimie Pure Et Appliquee. 81: 195-204. PMID 20046937 DOI: 10.1351/Pac-Con-08-07-03 |
0.41 |
|
2009 |
DeLorbe JE, Clements JH, Teresk MG, Benfield AP, Plake HR, Millspaugh LE, Martin SF. Thermodynamic and structural effects of conformational constraints in protein-ligand interactions. Entropic paradoxy associated with ligand preorganization. Journal of the American Chemical Society. 131: 16758-70. PMID 19886660 DOI: 10.1021/Ja904698Q |
0.752 |
|
2009 |
Smith AJ, Abbott LK, Martin SF. Enantioselective conjugate addition employing 2-heteroaryl titanates and zinc reagents. Organic Letters. 11: 4200-3. PMID 19708640 DOI: 10.1021/Ol9013975 |
0.439 |
|
2009 |
Knueppel D, Martin SF. Total synthesis of cribrostatin 6. Angewandte Chemie (International Ed. in English). 48: 2569-71. PMID 19235818 DOI: 10.1002/Anie.200806269 |
0.439 |
|
2009 |
Sunderhaus JD, Martin SF. Applications of multicomponent reactions to the synthesis of diverse heterocyclic scaffolds. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 1300-8. PMID 19132705 DOI: 10.1002/Chem.200802140 |
0.467 |
|
2009 |
Martin S, Smith A, Abbott L. Heteroaryl Titanates and Zinc Reagents in Enantioselective Conjugate Addition Synfacts. 2009: 1369-1369. DOI: 10.1055/S-0029-1218247 |
0.402 |
|
2008 |
Miller KA, Shanahan CS, Martin SF. The Pauson-Khand Reaction as a New Entry to the Synthesis of Bridged Bicyclic Heterocycles: Application to the Enantioselective Total Synthesis of (-)-Alstonerine. Tetrahedron. 64: 6884-6900. PMID 19122869 DOI: 10.1016/J.Tet.2008.02.066 |
0.742 |
|
2008 |
Simila ST, Martin SF. Applications of the Ugi reaction with ketones. Tetrahedron Letters. 49: 4501-4504. PMID 19122868 DOI: 10.1016/J.Tetlet.2008.05.073 |
0.818 |
|
2008 |
O'Keefe BM, Simmons N, Martin SF. Carbonylative cross-coupling of ortho-disubstituted aryl iodides. convenient synthesis of sterically hindered aryl ketones. Organic Letters. 10: 5301-4. PMID 18947231 DOI: 10.1021/Ol802202J |
0.423 |
|
2008 |
Davoren JE, Harcken C, Martin SF. Studies toward the enantioselective syntheses of oxylipins: total synthesis and structure revision of solandelactone E. The Journal of Organic Chemistry. 73: 391-402. PMID 18088137 DOI: 10.1021/Jo701739V |
0.799 |
|
2007 |
Sparks SM, Chen CL, Martin SF. Tandem Intramolecular Benzyne-Furan Cycloadditions. Total Synthesis of Vineomycinone B(2) Methyl Ester. Tetrahedron. 63: 8619-8635. PMID 18728697 DOI: 10.1016/J.Tet.2007.04.031 |
0.83 |
|
2007 |
Ashfeld BL, Miller KA, Smith AJ, Tran K, Martin SF. Features and applications of [Rh(CO)(2)Cl](2)-catalyzed alkylations of unsymmetrical allylic substrates. The Journal of Organic Chemistry. 72: 9018-31. PMID 17973524 DOI: 10.1021/Jo701290B |
0.811 |
|
2007 |
Pettersson M, Knueppel D, Martin SF. Concise, stereoselective approach to the spirooxindole ring system of citrinadin A. Organic Letters. 9: 4623-6. PMID 17918954 DOI: 10.1021/Ol702132V |
0.76 |
|
2007 |
Sunderhaus JD, Dockendorff C, Martin SF. Applications of multicomponent reactions for the synthesis of diverse heterocyclic scaffolds. Organic Letters. 9: 4223-6. PMID 17887692 DOI: 10.1021/Ol7018357 |
0.51 |
|
2007 |
Simila ST, Martin SF. Toward the total synthesis of FR901483: concise synthesis of the azatricyclic skeleton. The Journal of Organic Chemistry. 72: 5342-9. PMID 17555359 DOI: 10.1021/Jo070732A |
0.832 |
|
2007 |
Benfield AP, Whiddon BB, Clements JH, Martin SF. Structural and energetic aspects of Grb2-SH2 domain-swapping. Archives of Biochemistry and Biophysics. 462: 47-53. PMID 17466257 DOI: 10.1016/J.Abb.2007.03.010 |
0.772 |
|
2007 |
Benfield AP, Goodey NM, Phillips LT, Martin SF. Structural studies examining the substrate specificity profiles of PC-PLC(Bc) protein variants. Archives of Biochemistry and Biophysics. 460: 41-7. PMID 17324372 DOI: 10.1016/J.Abb.2007.01.023 |
0.773 |
|
2007 |
Miller KA, Martin SF. Concise, enantioselective total synthesis of (-)-alstonerine. Organic Letters. 9: 1113-6. PMID 17298078 DOI: 10.1021/Ol0700761 |
0.725 |
|
2007 |
Davoren JE, Martin SF. Enantioselective synthesis and structure revision of solandelactone E. Journal of the American Chemical Society. 129: 510-1. PMID 17227012 DOI: 10.1021/Ja068270Q |
0.793 |
|
2007 |
Martin S, Chen C, Sparks S. Synthesis of Vineomycinone B2 Methyl Ester Synfacts. 2007: 0236-0236. DOI: 10.1055/S-2007-968187 |
0.777 |
|
2007 |
Miller KA, Shanahan CS, Martin SF. Synthesis of (-)-Alstonerine Synfacts. 2007: 785-785. DOI: 10.1055/S-0028-1083565 |
0.702 |
|
2007 |
Breton P, Hergenrother PJ, Hida T, Hodgson A, Judd AS, Kraynack E, Kym PR, Lee WC, Loft MS, Yamashita M, Martin SF. Total synthesis of erythromycin B Tetrahedron. 63: 5709-5729. DOI: 10.1016/J.Tet.2007.02.044 |
0.645 |
|
2006 |
Chen CL, Sparks SM, Martin SF. C-Aryl glycosides via tandem intramolecular benzyne-furan cycloadditions. Total synthesis of vineomycinone B2 methyl ester. Journal of the American Chemical Society. 128: 13696-7. PMID 17044691 DOI: 10.1021/Ja0652619 |
0.811 |
|
2006 |
Benfield AP, Teresk MG, Plake HR, DeLorbe JE, Millspaugh LE, Martin SF. Ligand preorganization may be accompanied by entropic penalties in protein-ligand interactions. Angewandte Chemie (International Ed. in English). 45: 6830-5. PMID 17001728 DOI: 10.1002/Anie.200600844 |
0.741 |
|
2006 |
Deiters A, Pettersson M, Martin SF. General strategy for the syntheses of corynanthe, tacaman, and oxindole alkaloids. The Journal of Organic Chemistry. 71: 6547-61. PMID 16901143 DOI: 10.1021/Jo061032T |
0.824 |
|
2006 |
Reichelt A, Martin SF. Synthesis and properties of cyclopropane-derived peptidomimetics. Accounts of Chemical Research. 39: 433-42. PMID 16846207 DOI: 10.1021/Ar030255S |
0.636 |
|
2006 |
Chen CL, Martin SF. Pd-catalyzed ring opening of oxa- and azabicyclic alkenes with aryl and vinyl halides: efficient entry to 2-substituted 1,2-dihydro-1-naphthols and 2-substituted 1-naphthols. The Journal of Organic Chemistry. 71: 4810-7. PMID 16776506 DOI: 10.1021/Jo060299P |
0.658 |
|
2006 |
Brenneman JB, Martin SF. Ring-Closing Metathesis as a Construct for the Synthesis of Polycyclic Alkaloids Cheminform. 37. DOI: 10.2174/138527205774370478 |
0.442 |
|
2006 |
Li H, Procko K, Martin SF. Facile synthesis of C-aryl glycals from sugar-derived lactones Tetrahedron Letters. 47: 3485-3488. DOI: 10.1016/J.Tetlet.2006.02.150 |
0.466 |
|
2006 |
Simila ST, Reichelt A, Martin SF. Synthetic studies toward the immunosuppressant FR901483. Facile construction of the azatricyclic skeleton Tetrahedron Letters. 47: 2933-2936. DOI: 10.1016/J.Tetlet.2006.02.116 |
0.813 |
|
2006 |
Kummer DA, Brenneman JB, Martin SF. Domino intramolecular enyne metathesis/cross metathesis approach to the xanthanolides. Enantioselective synthesis of (+)-8-epi-xanthatin Tetrahedron. 62: 11437-11449. DOI: 10.1016/J.Tet.2006.05.019 |
0.512 |
|
2006 |
Li H, Procko K, Martin SF. Facile Synthesis of C-Aryl Glycals from Sugar-Derived Lactones. Cheminform. 37. DOI: 10.1002/CHIN.200635208 |
0.329 |
|
2006 |
Andrade RB, Martin SF. Formal Syntheses of (.+-.)-Pinnaic Acid (I) and (.+-.)-Halichlorine (II). Cheminform. 37. DOI: 10.1002/CHIN.200618201 |
0.555 |
|
2006 |
Ashfeld BL, Martin SF. Enantioselective Syntheses of Tremulenediol A (I) and Tremulenolide A (II). Cheminform. 37. DOI: 10.1002/chin.200607186 |
0.624 |
|
2005 |
Andrade RB, Martin SF. Formal syntheses of (+/-)-pinnaic acid and (+/-)-halichlorine. Organic Letters. 7: 5733-5. PMID 16321034 DOI: 10.1021/Ol0525009 |
0.655 |
|
2005 |
Kummer DA, Brenneman JB, Martin SF. Application of a domino intramolecular enyne metathesis/cross metathesis reaction to the total synthesis of (+)-8-epi-xanthatin. Organic Letters. 7: 4621-3. PMID 16209494 DOI: 10.1021/Ol051711A |
0.5 |
|
2005 |
Ashfeld BL, Martin SF. Enantioselective syntheses of tremulenediol A and tremulenolide A. Organic Letters. 7: 4535-7. PMID 16178577 DOI: 10.1016/J.Tet.2006.05.087 |
0.746 |
|
2005 |
Amorde SM, Judd AS, Martin SF. Cascade iminium ion reactions for the facile synthesis of quinolizidines. Concise syntheses of (+/-)-epilupinine and (-)-epimyrtine. Organic Letters. 7: 2031-3. PMID 15876047 DOI: 10.1021/Ol050544B |
0.815 |
|
2005 |
Ashfeld BL, Miller KA, Smith AJ, Tran K, Martin SF. [Rh(CO)2Cl]2-catalyzed domino reactions involving allylic substitution and subsequent carbocyclization reactions. Organic Letters. 7: 1661-3. PMID 15816777 DOI: 10.1021/Ol0504300 |
0.802 |
|
2005 |
Antikainen NM, Martin SF. Altering protein specificity: techniques and applications. Bioorganic & Medicinal Chemistry. 13: 2701-16. PMID 15781382 DOI: 10.1016/J.Bmc.2005.01.059 |
0.768 |
|
2005 |
Brenneman J, Martin S. Ring-Closing Metathesis as a Construct for the Synthesis of Polycyclic Alkaloids Current Organic Chemistry. 9: 1535-1549. DOI: 10.2174/138527205774370478 |
0.331 |
|
2005 |
Martin SF. Ring-Closing Metathesis: A Facile Construct for Alkaloid Synthesis Cheminform. 36. DOI: 10.1351/Pac200577071207 |
0.499 |
|
2005 |
Martin SF. Ring-closing metathesis: A facile construct for alkaloid synthesis Pure and Applied Chemistry. 77: 1207-1212. DOI: 10.1351/pac200577071207 |
0.4 |
|
2004 |
Chen CL, Martin SF. Facile synthesis of 2-substituted 1,2-dihydro-1-naphthols and 2-substituted 1-naphthols. Organic Letters. 6: 3581-4. PMID 15387553 DOI: 10.1021/Ol048517T |
0.676 |
|
2004 |
Deiters A, Martin SF. Synthesis of oxygen- and nitrogen-containing heterocycles by ring-closing metathesis. Chemical Reviews. 104: 2199-238. PMID 15137789 DOI: 10.1021/Cr0200872 |
0.609 |
|
2004 |
Brenneman JB, Martin SF. Application of intramolecular enyne metathesis to the synthesis of aza[4.2.1]bicyclics: enantiospecific total synthesis of (+)-anatoxin-a. Organic Letters. 6: 1329-31. PMID 15070329 DOI: 10.1021/Ol049631E |
0.473 |
|
2004 |
Ashfeld BL, Miller KA, Martin SF. Direct, stereoselective substitution in [Rh(CO)(2)Cl](2)-catalyzed allylic alkylations of unsymmetrical substrates. Organic Letters. 6: 1321-4. PMID 15070327 DOI: 10.1021/Ol0496529 |
0.779 |
|
2004 |
Kummer DA, Brenneman JB, Martin SF. An Efficient Synthesis of α-Branched Enones. Cheminform. 35. DOI: 10.1055/S-2004-829095 |
0.413 |
|
2004 |
Rudolph AC, Machauer R, Martin SF. Synthesis of cis-2,5-Disubstituted Pyrrolidines via Diastereoselective Reduction of N-Acyl Iminium Ions. Cheminform. 35. DOI: 10.1016/J.Tetlet.2004.04.122 |
0.401 |
|
2004 |
Brenneman JB, Machauer R, Martin SF. Enantioselective synthesis of (+)-anatoxin-a via enyne metathesis Tetrahedron. 60: 7301-7314. DOI: 10.1016/J.Tet.2004.06.021 |
0.462 |
|
2004 |
Brenneman JB, Machauer R, Martin SF. Enantioselective Synthesis of (+)-Anatoxin-a via Enyne Metathesis. Cheminform. 35. DOI: 10.1002/CHIN.200450170 |
0.376 |
|
2003 |
Neipp CE, Martin SF. Synthesis of bridged azabicyclic structures via ring-closing olefin metathesis. The Journal of Organic Chemistry. 68: 8867-78. PMID 14604356 DOI: 10.1021/Jo0349936 |
0.835 |
|
2003 |
Kaelin DE, Sparks SM, Plake HR, Martin SF. Regioselective synthesis of unsymmetrical C-aryl glycosides using silicon tethers as disposable linkers. Journal of the American Chemical Society. 125: 12994-5. PMID 14570450 DOI: 10.1021/Ja0375582 |
0.832 |
|
2003 |
Franklin CL, Li H, Martin SF. Design, synthesis, and evaluation of water-soluble phospholipid analogues as inhibitors of phospholipase C from Bacillus cereus. The Journal of Organic Chemistry. 68: 7298-307. PMID 12968879 DOI: 10.1021/Jo034411K |
0.301 |
|
2003 |
Washburn DG, Heidebrecht RW, Martin SF. Concise formal synthesis of (-)-peduncularine via ring-closing metathesis. Organic Letters. 5: 3523-5. PMID 12967315 DOI: 10.1021/Ol0354066 |
0.505 |
|
2003 |
Antikainen NM, Monzingo AF, Franklin CL, Robertus JD, Martin SF. Using X-ray crystallography of the Asp55Asn mutant of the phosphatidylcholine-preferring phospholipase C from Bacillus cereus to support the mechanistic role of Asp55 as the general base. Archives of Biochemistry and Biophysics. 417: 81-6. PMID 12921783 DOI: 10.1016/S0003-9861(03)00343-6 |
0.782 |
|
2003 |
Hergenrother PJ, Hodgson A, Judd AS, Lee WC, Martin SF. An abiotic strategy for the enantioselective synthesis of erythromycin B. Angewandte Chemie (International Ed. in English). 42: 3278-81. PMID 12876743 DOI: 10.1002/Anie.200351136 |
0.596 |
|
2003 |
Deiters A, Chen K, Eary CT, Martin SF. Biomimetic entry to the sarpagan family of indole alkaloids: total synthesis of +-geissoschizine and +-N-methylvellosimine. Journal of the American Chemical Society. 125: 4541-50. PMID 12683825 DOI: 10.1021/Ja0296024 |
0.673 |
|
2003 |
Antikainen NM, Hergenrother PJ, Harris MM, Corbett W, Martin SF. Altering substrate specificity of phosphatidylcholine-preferring phospholipase C of Bacillus cereus by random mutagenesis of the headgroup binding site. Biochemistry. 42: 1603-10. PMID 12578373 DOI: 10.1021/Bi0267285 |
0.771 |
|
2003 |
Martin SF. Unified strategy for the synthesis of C-aryl glycosides Pure and Applied Chemistry. 75: 63-70. DOI: 10.1351/Pac200375010063 |
0.485 |
|
2003 |
Plake HR, Sundberg TB, Woodward AR, Martin SF. Design and synthesis of conformationally constrained, extended and reverse turn pseudopeptides as Grb2-SH2 domain antagonists Tetrahedron Letters. 44: 1571-1574. DOI: 10.1016/S0040-4039(03)00013-3 |
0.783 |
|
2003 |
Apsel B, Bender JA, Escobar M, Kaelin DE, Lopez OD, Martin SF. General entries to C-aryl glycosides. Formal synthesis of galtamycinone Tetrahedron Letters. 44: 1075-1077. DOI: 10.1016/S0040-4039(02)02666-7 |
0.829 |
|
2003 |
Davidsen SK, Phllips GW, Martin SF. Geminal Acylation‐Alkylation at a Carbonyl Center Using Diethyl N‐Benzylideneaminomethylphosphonate: 2‐Methyl‐2‐Phenyl‐4‐Pentenal Organic Syntheses. 119-119. DOI: 10.1002/0471264180.Os065.16 |
0.36 |
|
2002 |
Martin SF. Evolution of the vinylogous Mannich reaction as a key construction for alkaloid synthesis. Accounts of Chemical Research. 35: 895-904. PMID 12379142 DOI: 10.1021/Ar950230W |
0.474 |
|
2002 |
Deiters A, Martin SF. Stereoselective total synthesis of dihydrocorynantheol. Organic Letters. 4: 3243-5. PMID 12227759 DOI: 10.1021/Ol026470A |
0.695 |
|
2002 |
Humphrey JM, Liao Y, Ali A, Rein T, Wong YL, Chen HJ, Courtney AK, Martin SF. Enantioselective total syntheses of manzamine a and related alkaloids. Journal of the American Chemical Society. 124: 8584-92. PMID 12121099 DOI: 10.1021/Ja0202964 |
0.839 |
|
2002 |
Naito S, Escobar M, Kym PR, Liras S, Martin SF. Novel approach to the zaragozic acids. Enantioselective total synthesis of 6,7-dideoxysqualestatin H5. The Journal of Organic Chemistry. 67: 4200-8. PMID 12054955 DOI: 10.1021/Jo011157S |
0.666 |
|
2002 |
Reichelt A, Gaul C, Frey RR, Kennedy A, Martin SF. Design, synthesis, and evaluation of matrix metalloprotease inhibitors bearing cyclopropane-derived peptidomimetics as P1' and P2' replacements. The Journal of Organic Chemistry. 67: 4062-75. PMID 12054939 DOI: 10.1021/Jo0110698 |
0.59 |
|
2002 |
Davidson JP, Lubman O, Rose T, Waksman G, Martin SF. Calorimetric and structural studies of 1,2,3-trisubstituted cyclopropanes as conformationally constrained peptide inhibitors of Src SH2 domain binding. Journal of the American Chemical Society. 124: 205-15. PMID 11782172 DOI: 10.1021/Ja011746F |
0.585 |
|
2002 |
Kitamura M, Oka H, Suga S, Noyori R, Kaelin DE, Martin SF, Beutner GL, Denmark SE. Catalytic enantioselective addition of dialkylzincs to aldehydes using (2s)-(-)-3-exo-(dimethylamino)isoborneol [(2S)DAIB]: (S)-1-phenyl-1-propanol Organic Syntheses. 79: 139-145. DOI: 10.15227/Orgsyn.079.0139 |
0.724 |
|
2002 |
Neipp CE, Martin SF. A ring-closing olefin metathesis approach to bridged azabicyclic structures Tetrahedron Letters. 43: 1779-1782. DOI: 10.1016/S0040-4039(02)00100-4 |
0.815 |
|
2002 |
Reichelt A, Bur SK, Martin SF. Applications of vinylogous Mannich reactions. Total synthesis of the angiotensin converting enzyme inhibitor (-)-A58365A Tetrahedron. 58: 6323-6328. DOI: 10.1016/S0040-4020(02)00631-2 |
0.827 |
|
2001 |
Kirkland TA, Colucci J, Geraci LS, Marx MA, Schneider M, Kaelin DE, Martin SF. Total synthesis of (+)-ambruticin S. Journal of the American Chemical Society. 123: 12432-3. PMID 11734054 DOI: 10.1016/S0040-4020(03)00370-3 |
0.8 |
|
2001 |
Harcken C, Martin SF. Improved E-selectivity in the Wittig reaction of stabilized ylides with alpha-alkoxyaldehydes and sugar lactols. Organic Letters. 3: 3591-3. PMID 11678716 DOI: 10.1021/Ol016729+ |
0.347 |
|
2001 |
Ito M, Clark CW, Mortimore M, Goh JB, Martin SF. Biogenetically inspired approach to the Strychnos alkaloids. Concise syntheses of (+/-)-akuammicine and (+/-)-strychnine. Journal of the American Chemical Society. 123: 8003-10. PMID 11506556 DOI: 10.1021/Ja010935V |
0.492 |
|
2001 |
Kaelin DE, Lopez OD, Martin SF. General strategies for the synthesis of the major classes of C-aryl glycosides. Journal of the American Chemical Society. 123: 6937-8. PMID 11448205 DOI: 10.1021/Ja0108640 |
0.762 |
|
2001 |
Neipp CE, Humphrey JM, Martin SF. The synthesis of homoallylic amines utilizing a cuprate-based 1,2-metalate rearrangement. The Journal of Organic Chemistry. 66: 531-7. PMID 11429825 DOI: 10.1021/Jo001386Z |
0.824 |
|
2001 |
Liras S, Lynch CL, Fryer AM, Vu BT, Martin SF. Applications of vinylogous Mannich reactions. Total syntheses of the Ergot alkaloids rugulovasines A and B and setoclavine. Journal of the American Chemical Society. 123: 5918-24. PMID 11414824 DOI: 10.1021/Ja010577W |
0.357 |
|
2001 |
Hillier MC, Davidson JP, Martin SF. Cyclopropane-derived peptidomimetics. design, synthesis, and evaluation of novel Ras farnesyltransferase inhibitors. The Journal of Organic Chemistry. 66: 1657-71. PMID 11262110 DOI: 10.1021/Jo001257I |
0.63 |
|
2001 |
Lee KL, Goh JB, Martin SF. Novel entry to the Ergot alkaloids via ring closing metathesis Tetrahedron Letters. 42: 1635-1638. DOI: 10.1016/S0040-4039(01)00002-8 |
0.453 |
|
2001 |
Bur SK, Martin SF. Vinylogous Mannich reactions: Selectivity and synthetic utility Tetrahedron. 57: 3221-3242. DOI: 10.1016/S0040-4020(01)00035-7 |
0.743 |
|
2001 |
Fellows IM, Kaelin Jr. DE, Martin SF. ChemInform Abstract: Application of Ring-Closing Metathesis to the Formal Total Synthesis of (+)-FR900482. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200113233 |
0.34 |
|
2000 |
Bur SK, Martin SF. Vinylogous Mannich reactions: some theoretical studies on the origins of diastereoselectivity. Organic Letters. 2: 3445-7. PMID 11082005 DOI: 10.1021/Ol006464J |
0.714 |
|
2000 |
Martin SF, Follows BC, Hergenrother PJ, Franklin CL. A novel class of zinc-binding inhibitors for the phosphatidylcholine-preferring phospholipase C from Bacillus cereus. The Journal of Organic Chemistry. 65: 4509-14. PMID 10959851 DOI: 10.1021/Jo9915731 |
0.546 |
|
2000 |
Martin SF, Chen KX, Eary CT. An enantioselective total synthesis of (+)-geissoschizine. Organic Letters. 1: 79-81. PMID 10822538 DOI: 10.1021/Ol990554A |
0.517 |
|
2000 |
Martin SF, Dwyer MP, Hartmann B, Knight KS. Cyclopropane-derived peptidomimetics. Design, synthesis, and evaluation of novel enkephalin analogues. The Journal of Organic Chemistry. 65: 1305-18. PMID 10814090 DOI: 10.1021/Jo991288H |
0.417 |
|
2000 |
Martin SF, Follows BC, Hergenrother PJ, Trotter BK. The choline binding site of phospholipase C (Bacillus cereus): insights into substrate specificity. Biochemistry. 39: 3410-5. PMID 10727235 DOI: 10.1021/Bi9919798 |
0.556 |
|
2000 |
Martin SF, DeBlanc RL, Hergenrother PJ. Determination of the substrate specificity of the phospholipase D from Streptomyces chromofuscus via an inorganic phosphate quantitation assay. Analytical Biochemistry. 278: 106-10. PMID 10660451 DOI: 10.1006/Abio.1999.4420 |
0.552 |
|
2000 |
Corley EG, Thompson AS, Huntington M, Hergenrother P, Martin SF. Cyclopropylacetylene: [Cyclopropane, ethynyl-] Organic Syntheses. 77. DOI: 10.15227/Orgsyn.077.0231 |
0.625 |
|
2000 |
Nifantiev EE, Gratchev MK, Martin SF. Regioselective monophosphorylation of glycols containing primary and secondary hydroxyl groups Mendeleev Communications. 10: 3-4. DOI: 10.1070/Mc2000V010N01Abeh001212 |
0.367 |
|
2000 |
Fellows IM, Kaelin DE, Martin SF. Application of ring-closing metathesis to the formal total synthesis of (+) - FR900482 Journal of the American Chemical Society. 122: 10781-10787. DOI: 10.1021/Ja0013879 |
0.795 |
|
2000 |
Davidson JP, Martin SF. Use of 1,2,3-trisubstituted cyclopropanes as conformationally constrained peptide mimics in SH2 antagonists Tetrahedron Letters. 41: 9459-9464. DOI: 10.1016/S0040-4039(00)01611-7 |
0.577 |
|
2000 |
Martin SF, Hillier MC. Applications of Intramolecular Cyclopropanations of Chiral Secondary Allylic Diazoacetates Journal of the Chinese Chemical Society. 47: 41-55. DOI: 10.1002/Jccs.200000004 |
0.319 |
|
1999 |
Lynch VM, Bur SK, Martin SF. Spiro[1-azabicyclo[5.3.0]decane-6,2'(5'H)-furan]-5',10-dione: an example of kryptoracemic crystallization. Acta Crystallographica. Section C, Crystal Structure Communications. 55: 622-4. PMID 10227127 DOI: 10.1107/S0108270198012748 |
0.703 |
|
1999 |
Martin SF, Hergenrother PJ. Catalytic cycle of the phosphatidylcholine-preferring phospholipase C from Bacillus cereus. Solvent viscosity, deuterium isotope effects, and proton inventory studies. Biochemistry. 38: 4403-8. PMID 10194360 DOI: 10.1021/Bi9821216 |
0.562 |
|
1999 |
Martin SF, Barr KJ, Smith DW, Bur SK. Applications of vinylogous Mannich reactions. Concise enantiospecific total syntheses of (+)-croomine Journal of the American Chemical Society. 121: 6990-6997. DOI: 10.1021/Ja990077R |
0.779 |
|
1999 |
Martin SF, Humphrey JM, Ali A, Hillier MC. Enantioselective Total Syntheses of Ircinal A and Related Manzamine Alkaloids Journal of the American Chemical Society. 121: 866-867. DOI: 10.1021/Ja9829259 |
0.372 |
|
1999 |
Martin SF, Lopez OD. Vinylogous Mannich reactions. Catalytic, asymmetric additions of triisopropylsilyloxyfurans to aldimines Tetrahedron Letters. 40: 8949-8953. DOI: 10.1016/S0040-4039(99)01939-5 |
0.723 |
|
1999 |
Martin SF, Hom RK, Dwyer MP. Synthesis of enantiomerically pure vinylcyclopropanes by SN2′ allylic carboxylate displacements Tetrahedron Letters. 40: 6721-6724. DOI: 10.1016/S0040-4039(99)01390-8 |
0.48 |
|
1999 |
Martin SF, Hom RK. Stereoselective elaboration of side chain residues in cyclopropane-containing dipeptide isosteres Tetrahedron Letters. 40: 2887-2890. DOI: 10.1016/S0040-4039(99)00397-4 |
0.364 |
|
1999 |
Martin SF, Bur SK. Vinylogous Mannich reactions. Stereoselective formal synthesis of pumiliotoxin 251D Tetrahedron. 55: 8905-8914. DOI: 10.1016/S0040-4020(99)00452-4 |
0.767 |
|
1999 |
Martin SF, Limberakis C, Burgess LE, Hartmann M. Strategies for ansamycin antibiotics. asymmetric synthesis of the C(3)–C(21) subunit of herbimycin A Tetrahedron. 55: 3561-3572. DOI: 10.1016/S0040-4020(98)01163-6 |
0.445 |
|
1998 |
Martin SF, Hergenrother PJ. Enzymatic synthesis of a modified phospholipid and its evaluation as a substrate for B. cereus phospholipase C. Bioorganic & Medicinal Chemistry Letters. 8: 593-6. PMID 9871566 DOI: 10.1016/S0960-894X(98)00071-7 |
0.616 |
|
1998 |
Martin SF, Hergenrother PJ. General base catalysis by the phosphatidylcholine-preferring phospholipase C from Bacillus cereus: the role of Glu4 and Asp55. Biochemistry. 37: 5755-60. PMID 9548962 DOI: 10.1021/Bi972948K |
0.566 |
|
1998 |
Martin SF, Naito S. Facile entry to the zaragozic acids. Asymmetric total synthesis of 6,7- dideoxysqualestatin H5 Journal of Organic Chemistry. 63: 7592-7593. DOI: 10.1021/Jo981684K |
0.357 |
|
1998 |
Martin SF, Hillier MC. Diastereodifferentiation in intramolecular cyclopropanations of chiral secondary allylic diazoacetates Tetrahedron Letters. 39: 2929-2932. DOI: 10.1016/S0040-4039(98)00501-2 |
0.309 |
|
1998 |
Martin SF, Dwyer MP. Iodocyclopropanes as versatile intermediates for the synthesis of substituted cyclopropanes Tetrahedron Letters. 39: 1521-1524. DOI: 10.1016/S0040-4039(98)00072-0 |
0.521 |
|
1998 |
Martin SF, Dwyer MP, Lynch CL. Application of AlMe3-mediated amidation reactions to solution phase peptide synthesis Tetrahedron Letters. 39: 1517-1520. DOI: 10.1016/S0040-4039(98)00071-9 |
0.409 |
|
1997 |
Hergenrother PJ, Martin SF. Determination of the kinetic parameters for phospholipase C (Bacillus cereus) on different phospholipid substrates using a chromogenic assay based on the quantitation of inorganic phosphate. Analytical Biochemistry. 251: 45-9. PMID 9300081 DOI: 10.1006/Abio.1997.2251 |
0.554 |
|
1997 |
Hergenrother PJ, Haas MK, Martin SF. Chromogenic assay for phospholipase D from Streptomyces chromofuscus: application to the evaluation of substrate analogs. Lipids. 32: 783-8. PMID 9252969 DOI: 10.1007/S11745-997-0101-5 |
0.542 |
|
1997 |
Martin SF. General strategies for the stereoselective synthesis of alkaloid natural products Pure and Applied Chemistry. 69: 571-576. DOI: 10.1351/Pac199769030571 |
0.383 |
|
1997 |
Martin SF, Hida T, Kym PR, Loft M, Hodgson A. The Asymmetric Synthesis of Erythromycin B Journal of the American Chemical Society. 119: 3193-3194. DOI: 10.1021/Ja963575Y |
0.364 |
|
1997 |
Martin SF, Bur SK. The stereochemical course of intramolecular vinylogous Mannich reactions Tetrahedron Letters. 38: 7641-7644. DOI: 10.1016/S0040-4039(97)10080-6 |
0.734 |
|
1997 |
Martin SF, Limberakis C. Diprotection of primary amines as N-substituted-2,5-bis[(triisopropylsilyl)oxy]pyrroles (BIPSOP) Tetrahedron Letters. 38: 2617-2620. DOI: 10.1016/S0040-4039(97)00443-7 |
0.344 |
|
1997 |
Martin SF, Anderson BG, Daniel D, Gaucher A. A cycloaddition approach to breynolide Tetrahedron. 53: 8997-9006. DOI: 10.1016/S0040-4020(97)90405-1 |
0.387 |
|
1996 |
Martin SF, Wagman AS. Synthesis and Kinetic Evaluation of Inhibitors of the Phosphatidylinositol-Specific Phospholipase C from Bacillus cereus. The Journal of Organic Chemistry. 61: 8016-8023. PMID 11667784 DOI: 10.1021/Jo960850Q |
0.374 |
|
1996 |
Martin SF, Spaller MR, Hergenrother PJ. Expression and site-directed mutagenesis of the phosphatidylcholine-preferring phospholipase C of Bacillus cereus: probing the role of the active site Glu146. Biochemistry. 35: 12970-7. PMID 8841144 DOI: 10.1021/Bi961316F |
0.566 |
|
1996 |
Martin SF, Barr KJ. Vinylogous Mannich reactions. The asymmetric total synthesis of (+)-croomine Journal of the American Chemical Society. 118: 3299-3300. DOI: 10.1021/Ja9542146 |
0.466 |
|
1996 |
Martin SF, Chen HJ, Courtney AK, Liao Y, Pätzel M, Ramser MN, Wagman AS. Ring-closing olefin metathesis for the synthesis of fused nitrogen heterocycles Tetrahedron. 52: 7251-7264. DOI: 10.1016/0040-4020(96)00249-9 |
0.827 |
|
1996 |
Martin SF, Dodge JA, Burgess LE, Limberakis C, Hartmann M. Novel approach to the ansamycin antibiotics macbecin I and herbimycin A. A formal total synthesis of (+)-macbecin I Tetrahedron. 52: 3229-3246. DOI: 10.1016/0040-4020(95)01107-2 |
0.472 |
|
1995 |
Hergenrother PJ, Spaller MR, Haas MK, Martin SF. Chromogenic assay for phospholipase C from Bacillus cereus. Analytical Biochemistry. 229: 313-6. PMID 7485988 DOI: 10.1006/Abio.1995.1418 |
0.508 |
|
1995 |
Martin SF, Clark CW, Corbett JW. Applications of Vinylogous Mannich Reactions. Asymmetric Synthesis of the Heteroyohimboid Alkaloids (-)-Ajmalicine, (+)-19-epi-Ajmalicine, and (-)-Tetrahydroalstonine The Journal of Organic Chemistry. 60: 3236-3242. DOI: 10.1021/Jo00115A044 |
0.458 |
|
1995 |
Martin SF, Chen H, Lynch VM. Asymmetric Synthesis of 1-Deoxy-8,8a-di-epi-castanospermine The Journal of Organic Chemistry. 60: 276-278. DOI: 10.1021/Jo00106A051 |
0.332 |
|
1995 |
Doyle MP, Dyatkin AB, Kalinin AV, Ruppar DA, Martin SF, Spaller MR, Liras S. Highly selective enantiomer differentiation in intramolecular cyclopropanation reactions of racemic secondary allylic diazoacetates. Journal of the American Chemical Society. 117: 11021-11022. DOI: 10.1021/Ja00149A031 |
0.407 |
|
1995 |
Martin SF, Wagman AS. A novel approach to FR-900482 via ring forming metathesis Tetrahedron Letters. 36: 1169-1170. DOI: 10.1016/0040-4039(94)02488-W |
0.382 |
|
1995 |
Martin S, Assercq J, Austin R, Dantanarayana A, Fishpaugh J, Gluchowski C, Guinn D, Hartmann M, Tanaka T, Wagner R, White J. Facile access to the ABC ring system of the taxane diterpenes via anionic oxy-Cope rearrangements Tetrahedron. 51: 3455-3482. DOI: 10.1016/0040-4020(95)00095-P |
0.432 |
|
1994 |
Lynch VM, Lee WC, Martin SF, Davis BE. A novel dioxabicyclo[3.3.1]nonane, a key intermediate in the synthesis of erythronolide B seco-acid. Acta Crystallographica. Section C, Crystal Structure Communications. 1467-9. PMID 7946151 DOI: 10.1107/S0108270193012880 |
0.335 |
|
1994 |
Martin SF, Wagman AS, Zipp GG, Gratchev MK. General Route to Phosphonodithioic Acid Derivatives The Journal of Organic Chemistry. 59: 7957-7958. DOI: 10.1021/Jo00105A007 |
0.316 |
|
1994 |
Martin SF, Wong Y, Wagman AS. Design, Synthesis, and Evaluation of Phospholipid Analogs as Inhibitors of the Bacterial Phospholipase C from Bacillus cereus The Journal of Organic Chemistry. 59: 4821-4831. DOI: 10.1021/Jo00096A024 |
0.318 |
|
1994 |
Martin SF, Josey JA, Wong Y, Dean DW. General Method for the Synthesis of Phospholipid Derivatives of 1,2-O-Diacyl-sn-Glycerols The Journal of Organic Chemistry. 59: 4805-4820. DOI: 10.1021/Jo00096A023 |
0.404 |
|
1994 |
Martin SF, Lee W, Pacofsky GJ, Gist RP, Mulhern TA. Strategies for Macrolide Synthesis. A Concise Approach to Protected Seco-Acids of Erythronolides A and B Journal of the American Chemical Society. 116: 4674-4688. DOI: 10.1021/Ja00090A016 |
0.363 |
|
1994 |
Martin SF, Spaller MR, Liras S, Hartmann B. Enantio- and Diastereoselectivity in the Intramolecular Cyclopropanation of Secondary Allylic Diazoacetates Journal of the American Chemical Society. 116: 4493-4494. DOI: 10.1021/Ja00089A055 |
0.452 |
|
1994 |
Martin SF, Liao Y, Wong Y, Rein T. A novel approach to the asymmetric synthesis of manzamine A. Construction of the tetracyclic ABCE ring system Tetrahedron Letters. 35: 691-694. DOI: 10.1016/S0040-4039(00)75792-3 |
0.485 |
|
1994 |
Martin SF, Liao Y, Chen H, Pätzel M, Ramser MN. Novel route to fused nitrogen heterocycles by olefin metathesis Tetrahedron Letters. 35: 6005-6008. DOI: 10.1016/0040-4039(94)88060-3 |
0.455 |
|
1994 |
Martin SF. Strategies for the synthesis of heterocyclic natural products Journal of Heterocyclic Chemistry. 31: 679-686. DOI: 10.1002/Jhet.5570310308 |
0.377 |
|
1993 |
Hansen S, Hough E, Svensson LA, Wong YL, Martin SF. Crystal structure of phospholipase C from Bacillus cereus complexed with a substrate analog. Journal of Molecular Biology. 234: 179-87. PMID 8230197 DOI: 10.1006/Jmbi.1993.1572 |
0.334 |
|
1993 |
Martin SF. Strategies and tactics for the synthesis of oxygenated natural products. Journal of Natural Products. 55: 1718-31. PMID 1294694 DOI: 10.1021/Np50090A002 |
0.469 |
|
1993 |
Martin SF, Wagman AS. A general and efficient route to phosphorodithioate analogs of naturally occurring lipids The Journal of Organic Chemistry. 58: 5897-5899. DOI: 10.1021/Jo00074A012 |
0.357 |
|
1993 |
Martin SF, Chen HJ, Yang CP. Facile asymmetric syntheses of 1-deoxycastanospermine and 1-deoxy-8a-epi-castanospermine The Journal of Organic Chemistry. 58: 2867-2873. DOI: 10.1021/Jo00062A035 |
0.409 |
|
1993 |
Martin SF, Liras S. Novel applications of vinylogous Mannich reactions. Total synthesis of rugulovasines A and B Journal of the American Chemical Society. 115: 10450-10451. DOI: 10.1021/Ja00075A107 |
0.42 |
|
1993 |
Martin SF, Daniel D. A novel approach to breynolide Tetrahedron Letters. 34: 4281-4284. DOI: 10.1016/S0040-4039(00)79329-4 |
0.383 |
|
1993 |
Martin SF, Lee W. Effect of metal counterions on the stereoselectivity of aldol reactions used to assemble the seco acid backbone of erythromycin b Tetrahedron Letters. 34: 2711-2714. DOI: 10.1016/S0040-4039(00)73542-8 |
0.428 |
|
1993 |
Martin SF, Hartmann M, Josey JA. Erratum: 'Diastereoselective [4+2] cycloadditions of acyl nitroso compounds (Tetrahedron letters (1992) 33 (3583)) Tetrahedron Letters. 34. DOI: 10.1016/S0040-4039(00)60464-1 |
0.318 |
|
1993 |
Martin SF, Oalmann CJ, Liras S. Cyclopropanes as conformationally restricted peptide isosteres. Design and synthesis of novel collagenase inhibitors Tetrahedron. 49: 3521-3532. DOI: 10.1016/S0040-4020(01)90212-1 |
0.475 |
|
1992 |
Lynch VM, Liao Y, Martin SF, Davis BE. Structure of a tricyclic subunit of manzamine A. Acta Crystallographica. Section C, Crystal Structure Communications. 1703-5. PMID 1445680 DOI: 10.1107/S0108270192001045 |
0.301 |
|
1992 |
Lynch VM, Corbett JW, Martin SF, Davis BE. Structure of a chiral intermediate in the synthesis of (+)-19-epiajmalicine. Acta Crystallographica. Section C, Crystal Structure Communications. 48: 1878-80. PMID 1445675 DOI: 10.1107/S0108270192002336 |
0.315 |
|
1992 |
Martin SF, Corbett JW. The Stereochemical Course of Nucleophilic Additions of 2-Trialkylsiloxyfurans to CyclicN-Acyliminium Ions Synthesis. 1992: 55-57. DOI: 10.1055/S-1992-34157 |
0.308 |
|
1992 |
Martin SF, Daniel D, Cherney RJ, Liras S. A convergent method for the stereoselective synthesis of trisubstituted alkenes The Journal of Organic Chemistry. 57: 2523-2525. DOI: 10.1021/Jo00035A004 |
0.432 |
|
1992 |
Martin SF, Dodge JA, Burgess LE, Hartmann M. A formal total synthesis of (+)-macbecin I The Journal of Organic Chemistry. 57: 1070-1072. DOI: 10.1021/Jo00030A007 |
0.453 |
|
1992 |
Martin SF, Hartmann M, Josey JA. Diastereoselective [4+2] Cycloadditions of Acyl Nitroso Compounds Tetrahedron Letters. 33: 3583-3586. DOI: 10.1016/S0040-4039(00)92508-5 |
0.382 |
|
1992 |
Martin SF, Dean DW, Wagman AS. A general method for the synthesis of 1,1-difluoroalkylphosphonates Tetrahedron Letters. 33: 1839-1842. DOI: 10.1016/S0040-4039(00)74156-6 |
0.383 |
|
1992 |
Martin SF, Oalmann CJ, Liras S. Enantioselective, rhodium catalyzed intramolecular cyclopropanations of homoallylic diazoacetates. Tetrahedron Letters. 33: 6727-6730. DOI: 10.1016/S0040-4039(00)61761-6 |
0.383 |
|
1991 |
Lynch VM, Zinke PW, Martin SF, Davis BE. Structure of a key intermediate in the asymmetric synthesis of (+)-KDO. Acta Crystallographica. Section C, Crystal Structure Communications. 910-2. PMID 1863428 DOI: 10.1107/S0108270190011039 |
0.34 |
|
1991 |
Martin SF, Zinke PW. The furan approach to oxygenated natural products. Total synthesis of (+)-KDO The Journal of Organic Chemistry. 56: 6600-6606. DOI: 10.1021/Jo00023A028 |
0.324 |
|
1991 |
Martin SF, Li W. Applications of intramolecular Diels-Alder reactions to alkaloid synthesis. A formal total synthesis of (.+-.)-dendrobine The Journal of Organic Chemistry. 56: 642-650. DOI: 10.1021/Jo00002A029 |
0.482 |
|
1991 |
Martin SF, Hunter JE, Benage B, Geraci LS, Mortimore M. Unified strategy for synthesis of indole and 2-oxindole alkaloids Journal of the American Chemical Society. 113: 6161-6171. DOI: 10.1021/Ja00016A036 |
0.437 |
|
1991 |
Martin SF, Yamashita M. Novel macrolactonization strategy for the synthesis of erythromycin antibiotics Journal of the American Chemical Society. 113: 5478-5480. DOI: 10.1021/Ja00014A063 |
0.321 |
|
1991 |
Doyle MP, Pieters RJ, Martin SF, Austin RE, Oalmann CJ, Mueller P. High enantioselectivity in the intramolecular cyclopropanation of allyl diazoacetates using a novel rhodium(II) catalyst Journal of the American Chemical Society. 113: 1423-1424. DOI: 10.1021/Ja00004A059 |
0.313 |
|
1991 |
Martin SF, Dodge JA. Efficacious modification of the mitsunobu reaction for inversions of sterically hindered secondary alcohols Tetrahedron Letters. 32: 3017-3020. DOI: 10.1016/0040-4039(91)80675-V |
0.315 |
|
1991 |
Martin SF, Rein T, Liao Y. Construction of the tricyclic ABC ring subunit of manzamine A via a novel intramolecular Diels-Alder reaction Tetrahedron Letters. 32: 6481-6484. DOI: 10.1016/0040-4039(91)80198-F |
0.433 |
|
1990 |
Lynch VM, Li W, Martin SF, Davis BE. Dendrobine support studies. The structure of a novel 3-azatricyclo[6.2.1.0(4,11)]-undecane derivative. Acta Crystallographica. Section C, Crystal Structure Communications. 1155-7. PMID 1975499 DOI: 10.1107/S0108270190000828 |
0.308 |
|
1990 |
Martin SF, Austin RE, Oalmann CJ. Stereoselective synthesis of 1,2,3-trisubstituted cyclopropanes as novel dipeptide isosteres Tetrahedron Letters. 31: 4731-4734. DOI: 10.1016/S0040-4039(00)97718-9 |
0.428 |
|
1990 |
Martin SF, Mortimore M. New methods for the synthesis of oxindole alkaloids. Total syntheses of isopteropodine and pteropodine. Tetrahedron Letters. 31: 4557-4560. DOI: 10.1016/S0040-4039(00)97675-5 |
0.388 |
|
1990 |
MARTIN SF, CHEAVENS TH. ChemInform Abstract: Synthesis of Polycyclic Lactams via Intramolecular Dipolar Cycloadditions of Stabilized Azomethine Ylides. Cheminform. 21. DOI: 10.1002/CHIN.199030077 |
0.325 |
|
1989 |
Martin SF, Colapret JA, Dappen MS, Dupre B, Murphy CJ. Application of nitrile oxide cycloadditions to a convergent, asymmetric synthesis of (+)-phyllanthocin The Journal of Organic Chemistry. 54: 2209-2216. DOI: 10.1021/Jo00270A035 |
0.351 |
|
1989 |
Martin SF, Li W. General methods for alkaloid synthesis via intramolecular Diels-Alder reactions. A concise formal total synthesis of (.+-.)-dendrobine The Journal of Organic Chemistry. 54: 265-268. DOI: 10.1021/Jo00263A002 |
0.483 |
|
1989 |
Martin SF, Pacofsky GJ, Gist RP, Lee WC. A concise asymmetric synthesis of the seco-acid of erythronolide B Journal of the American Chemical Society. 111: 7634-7636. DOI: 10.1021/Ja00201A066 |
0.405 |
|
1989 |
Martin SF, Zinke PW. The furan approach to higher monosaccharides. A concise total synthesis of (+)-KDO Journal of the American Chemical Society. 111: 2311-2313. DOI: 10.1021/Ja00188A060 |
0.393 |
|
1989 |
Martin SF, Cheavens TH. Synthesis of polycyclic lactams via intramolecular dipolar cycloadditions of stabilized azomethine ylides Tetrahedron Letters. 30: 7017-7020. DOI: 10.1016/S0040-4039(01)93412-4 |
0.463 |
|
1989 |
Martin SF. Chapter 9 - A Unified Strategy for the Synthesis of Alkaloids of the Yohimboid, Heteroyohimboid, and Corynantheioid Families Strategies and Tactics in Organic Synthesis. 2: 291-322. DOI: 10.1016/B978-0-08-092429-8.50014-3 |
0.324 |
|
1989 |
MARTIN SF, LI W. ChemInform Abstract: General Methods for Alkaloid Synthesis via Intramolecular Diels-Alder Reactions. A Concise Formal Total Synthesis of (.+-.)-Dendrobine. Cheminform. 20. DOI: 10.1002/CHIN.198934335 |
0.386 |
|
1989 |
MARTIN SF, GERACI LS. ChemInform Abstract: Concise Approach to the Aromatic Yohimboid and Protoberberine Alkaloids via Intramolecular Diels-Alder Reactions. Cheminform. 20. DOI: 10.1002/CHIN.198932300 |
0.303 |
|
1988 |
Martin SF, Campbell CL. Total syntheses of (.+-.)-crinine and (.+-.)-buphanisine The Journal of Organic Chemistry. 53: 3184-3190. DOI: 10.1021/Jo00249A011 |
0.369 |
|
1988 |
Martin SF, Fishpaugh JR, Power JM, Giolando DM, Jones RA, Nunn CM, Cowley AH. Structure and reactivity of novel lithium di-tert-butylphosphido(alkyl)cuprates Journal of the American Chemical Society. 110: 7226-7228. DOI: 10.1021/Ja00229A054 |
0.369 |
|
1988 |
Martin SF, Benage B, Hunter JE. A concise strategy for the syntheses of indole alkaloids of the heteroyohimboid and corynantheioid families. Total syntheses of (.+-.)-tetrahydroalstonine, (.+-.)-cathenamine and (.+-.)-geissoschizine Journal of the American Chemical Society. 110: 5925-5927. DOI: 10.1021/Ja00225A068 |
0.325 |
|
1988 |
Martin SF, Campbell CL. Total syntheses of (±)-crinine and (±)-buphanisine Journal of Organic Chemistry. 53: 3184-3190. DOI: 10.1016/S0040-4039(00)95766-6 |
0.345 |
|
1988 |
Martin SF, Geraci LS. Concise approach to the aromatic yohimboid and protoberberine alkaloids via intramolecular Diels-Alder reactions Tetrahedron Letters. 29: 6725-6728. DOI: 10.1016/S0040-4039(00)82439-9 |
0.482 |
|
1988 |
Martin SF, Yang C, Laswell WL, Rüeger H. Application of reductive, single electron transfer processes to the generation and cyclization of ω-unsaturated α-amino radicals Tetrahedron Letters. 29: 6685-6687. DOI: 10.1016/S0040-4039(00)82428-4 |
0.332 |
|
1988 |
Martin SF, Josey JA. A general protocol for the preparation of phospholipids via phosphite coupling Tetrahedron Letters. 29: 3631-3634. DOI: 10.1016/S0040-4039(00)82140-1 |
0.391 |
|
1988 |
Martin SF, Gluchowski C, Campbell CL, Chapman RC. A concise route to a key intermediate in the total syntheses of (+)-tirandamycic acid and (-)-tirandamycin a † Tetrahedron. 44: 3171-3180. DOI: 10.1016/S0040-4020(01)85948-2 |
0.691 |
|
1988 |
MARTIN SF, GUINN DE. ChemInform Abstract: A Stereoselective Synthesis of (+)-Prelog-Djerassi Lactone (I) from Furanoid Intermediates. Cheminform. 19. DOI: 10.1002/CHIN.198818206 |
0.382 |
|
1987 |
Martin SF, Dappen MS, Dupre B, Murphy CJ. A convergent total synthesis of (+)-phyllanthocin The Journal of Organic Chemistry. 52: 3706-3708. DOI: 10.1021/Jo00392A046 |
0.406 |
|
1987 |
Martin SF, Guinn DE. Stereoselective synthesis of (+)-Prelog-Djerassi lactone from furanoid intermediates The Journal of Organic Chemistry. 52: 5588-5593. DOI: 10.1021/Jo00234A015 |
0.491 |
|
1987 |
Martin SF, Davidsen SK, Puckette TA. Total syntheses of the amaryllidaceae alkaloids (.+-.)-hemanthidine and (.+-.)-pretazettine The Journal of Organic Chemistry. 52: 1962-1972. DOI: 10.1021/Ja00333A061 |
0.386 |
|
1987 |
Martin SF, Rueger H, Williamson SA, Grzejszczak S. General strategies for the synthesis of indole alkaloids. Total synthesis of (.+-.)-reserpine and (.+-.)-.alpha.-yohimbine Journal of the American Chemical Society. 109: 6124-6134. DOI: 10.1021/Ja00254A036 |
0.381 |
|
1987 |
MARTIN SF, CAMPBELL CL. ChemInform Abstract: Total Synthesis of (.+-.)-Crinine (IIa) and (.+-.)-Buphanisine (IIb). Cheminform. 18. DOI: 10.1002/CHIN.198728328 |
0.321 |
|
1986 |
Martin SF, Benage B, Williamson SA, Brown SP. Applications of the intramolecular diels-alder reactions of heterodienes to the syntheses of indole alkaloids Tetrahedron. 42: 2903-2910. DOI: 10.1016/S0040-4020(01)90579-4 |
0.44 |
|
1986 |
Sutko JL, Thompson LJ, Schlatterer RG, Lattanzio FA, Fairhurst AS, Campbell C, Martin SF, Deslongehamps P, Ruest L, Taylor DR. Separation and formation of ryanodine from dehydroryanodine. Preparation of tritium‐labeled ryanodine Journal of Labelled Compounds and Radiopharmaceuticals. 23: 215-222. DOI: 10.1002/Jlcr.2580230212 |
0.333 |
|
1986 |
MARTIN SF, BENAGE B, WILLIAMSON SA, BROWN SP. ChemInform Abstract: Applications of the Intramolecular Diels-AldEr Reactions of Heterodienes to the Syntheses of Indole Alkaloids. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198641323 |
0.326 |
|
1985 |
Martin SF, Grzejszczak S, Rueeger H, Williamson SA. Total synthesis of (.+-.)-reserpine Journal of the American Chemical Society. 107: 4072-4074. DOI: 10.1021/Ja00299A050 |
0.429 |
|
1985 |
Martin SF, Rüeger H. Total synthesis of α-yohimbine Tetrahedron Letters. 26: 5227-5230. DOI: 10.1016/S0040-4039(00)95001-9 |
0.365 |
|
1985 |
MARTIN SF, GRZEJSZCZAK S, RUEEGER H, WILLIAMSON SA. ChemInform Abstract: TOTAL SYNTHESIS OF (.+-.)-RESERPINE Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198543350 |
0.431 |
|
1985 |
MARTIN SF, BENAGE B. ChemInform Abstract: APPLICATIONS OF INTRAMOLECULAR DIELS-ALDER REACTIONS OF HETERODIENES. FACILE SYNTHESES OF THE HETEROYOHIMBINE ALKALOIDS TETRAHYDROALSTONINE AND AKUAMMIGINE Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198510345 |
0.32 |
|
1985 |
MARTIN SF, DAVIDSEN SK. ChemInform Abstract: TOTAL SYNTHESES OF THE AMARYLLIDACEAE ALKALOIDS (.+-.)-HAEMANTHIDINE AND (.+-.)-PRETAZETTINE Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198506341 |
0.378 |
|
1984 |
Martin SF, Guinn DE. Furans as intermediates for the synthesis of oxygenated natural products. Asymmetric synthesis of Prelog-Djerassi lactone. Tetrahedron Letters. 25: 5607-5610. DOI: 10.1016/S0040-4039(01)91392-9 |
0.454 |
|
1984 |
Martin SF, Benage B. Applications of intramolecular diels-alder reactions of heterodienes. Facile syntheses of the heteroyohimbine alkaloids tetrahydroalstonine and akuammigine. Tetrahedron Letters. 25: 4863-4866. DOI: 10.1016/S0040-4039(01)91244-4 |
0.453 |
|
1984 |
MARTIN SF, GLUCHOWSKI C, CAMPBELL CL, CHAPMAN RC. ChemInform Abstract: FURANS AS INTERMEDIATES FOR THE SYNTHESIS OF OXYGENATED NATURAL PRODUCTS. A FORMAL ASYMMETRIC SYNTHESIS OF (+)-TIRANDAMYCIC ACID Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198449335 |
0.303 |
|
1984 |
Martin SF, Gluchowski C, Campbell CL, Chapman RC. Furans as intermediates for the synthesis of oxygenated natural products. A formal asymmetric synthesis of (+)-tirandamycic acid The Journal of Organic Chemistry. 49: 2512-2513. DOI: 10.1002/Chin.198449335 |
0.662 |
|
1984 |
MARTIN SF, WILLIAMSON SA, GIST RP, SMITH KM. ChemInform Abstract: ASPECTS OF THE INTRAMOLECULAR DIELS-ALDER REACTIONS OF SOME 1,3,9-TRIENIC AMIDES, AMINES, AND ESTERS. AN APPROACH TO THE PENTACYCLIC SKELETON OF THE YOHIMBOID ALKALOIDS Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198423125 |
0.335 |
|
1983 |
Martin SF, Dupre B. Regiochemistry of the dipolar cycloadditions of nitrile oxides to unactivated olefins. Application to the stereoselective elaboration of β-hydroxycarbonyl compounds. Tetrahedron Letters. 24: 1337-1340. DOI: 10.1016/S0040-4039(00)81650-0 |
0.337 |
|
1983 |
Martin SF, Williamson SA, Gist RP, Smith KM. Aspects of the intramolecular Diels-Alder reactions of some 1,3,9-trienic amides, amines, and esters. An approach to the pentacyclic skeleton of the yohimboid alkaloids The Journal of Organic Chemistry. 48: 5170-5180. DOI: 10.1002/Chin.198423125 |
0.437 |
|
1982 |
Martin SF, Garrison PJ. Synthesis and Some Reactions of Diethyl 1-Methylthio-1(Z),3-butadienephosphonate Synthesis. 1982: 394-397. DOI: 10.1055/S-1982-29810 |
0.445 |
|
1982 |
Martin SF, Tu C, Kimura M, Simonsen SH. Intramolecular [4+2] cycloadditions as a general strategy for alkaloid synthesis. A novel formal synthesis of lycorine The Journal of Organic Chemistry. 47: 3634-3643. DOI: 10.1021/Jo00140A008 |
0.472 |
|
1982 |
Martin SF, White JB, Wagner R. Alkoxide-accelerated sigmatropic rearrangements. A novel entry to the bicyclo[5.3.1]undec-7-ene system of the taxane diterpenes The Journal of Organic Chemistry. 47: 3190-3192. DOI: 10.1021/Jo00137A039 |
0.359 |
|
1982 |
Martin SF, White JB. Intramolecular photochemical [2+2] cycloadditions. Regiochemistry of the photocyclizations of some oxygen-substituted 6-allylcyclohexenones Tetrahedron Letters. 23: 23-26. DOI: 10.1016/S0040-4039(00)97522-1 |
0.323 |
|
1982 |
MARTIN SF, GARRISON PJ. ChemInform Abstract: GENERAL METHODS FOR ALKALOID SYNTHESIS. TOTAL SYNTHESIS OF RACEMIC LYCORAMINE Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198237331 |
0.325 |
|
1982 |
Martin SF, Garrison PJ. General methods for alkaloid synthesis. Total synthesis of racemic lycoramine The Journal of Organic Chemistry. 47: 1513-1518. DOI: 10.1002/Chin.198237331 |
0.43 |
|
1982 |
MARTIN SF, GARRISON PJ. ChemInform Abstract: SYNTHESIS AND SOME REACTIONS OF DIETHYL 1-METHYLTHIO-1(Z),3-BUTADIENEPHOSPHONATE Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198237242 |
0.349 |
|
1982 |
MARTIN SF, TU C. ChemInform Abstract: GENERAL STRATEGIES FOR ALKALOID SYNTHESIS VIA INTRAMOLECULAR (4 + 2) CYCLOADDITIONS OF ENAMIDES. APPLICATION TO THE FORMAL TOTAL SYNTHESIS OF RACEMIC LYCORINE Chemischer Informationsdienst. 13. DOI: 10.1002/CHIN.198205331 |
0.361 |
|
1982 |
MARTIN SF, GARRISON PJ. ChemInform Abstract: TOTAL SYNTHESIS OF RACEMIC LYCORAMINE Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198202334 |
0.33 |
|
1981 |
Martin SF, Tu C. General strategies for alkaloid synthesis via intramolecular [4 + 2] cycloadditions of enamides. Application to the formal total synthesis of racemic lycorine The Journal of Organic Chemistry. 46: 3763-3764. DOI: 10.1021/Jo00331A049 |
0.463 |
|
1981 |
Martin SF, Garrison PJ. Total synthesis of racemic lycoramine The Journal of Organic Chemistry. 46: 3567-3568. DOI: 10.1021/Jo00330A045 |
0.441 |
|
1980 |
MARTIN SF, TU C, CHOU T. ChemInform Abstract: NOVEL INTRAMOLECULAR (4 + 2) CYCLOADDITION REACTIONS OF ENAMINES AND ENAMIDES WITH UNACTIVATED DIENES Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198045102 |
0.322 |
|
1980 |
Martin SF, Tu C, Chou T. Novel intramolecular [4 + 2] cycloaddition reactions of enamines and enamides with unactivated dienes Journal of the American Chemical Society. 102: 5274-5279. DOI: 10.1002/Chin.198045102 |
0.424 |
|
1980 |
MARTIN SF, DESAI SR, PHILLIPS GW, MILLER AC. ChemInform Abstract: GENERAL METHODS FOR ALKALOID SYNTHESIS VIA INTRAMOLECULAR (4 + 2) CYCLOADDITION REACTIONS OF ENAMIDES. A NEW APPROACH TO THE SYNTHESIS OF ASPIDOSPERMA ALKALOIDS Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198030333 |
0.376 |
|
1980 |
Martin SF, Desai SR, Philips GW, Miller AC. General methods for alkaloid synthesis via intramolecular [4 + 2] cycloaddition reactions of enamides. A new approach to the synthesis of Aspidosperma alkaloids Journal of the American Chemical Society. 102: 3294-3296. DOI: 10.1002/Chin.198030333 |
0.474 |
|
1980 |
MARTIN SF, PUCKETTE TA, COLAPRET JA. ChemInform Abstract: NEW METHODS FOR ALKALOID SYNTHESIS. FACILE TOTAL SYNTHESES OF (.+-.)-O-METHYLJOUBERTIAMINE AND (.+-.)-MESEMBRINE Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198004364 |
0.354 |
|
1979 |
Martin SF. Synthesis of Aldehydes, Ketones, and Carboxylic Acids from Lower Carbonyl Compounds by C-C Coupling Reactions Synthesis. 1979: 633-665. DOI: 10.1055/S-1979-28789 |
0.436 |
|
1979 |
Martin SF, Puckette TA, Colapret JA. New methods for alkaloid synthesis. Facile total syntheses of (.+-.)-O-methyljoubertiamine and (.+-.)-mesembrine The Journal of Organic Chemistry. 44: 3391-3396. DOI: 10.1021/Jo01333A025 |
0.344 |
|
1979 |
Martin SF, Chou T, Tu C. Intramolecular [4+2] cycloaddition reactions of enamines and enamides Tetrahedron Letters. 20: 3823-3826. DOI: 10.1016/S0040-4039(01)95534-0 |
0.472 |
|
1979 |
MARTIN SF, DESAI SR. ChemInform Abstract: HETEROATOM-SUBSTITUTED BUTADIENYLPHOSPHONIUM SALTS AS REAGENTS. A NEW SYNTHESIS OF 2-ETHOXYCYCLOHEXADIENES AND CYCLOHEXENONES Chemischer Informationsdienst. 10. DOI: 10.1002/chin.197915189 |
0.349 |
|
1978 |
Martin SF, Puckette TA. A facile synthesis of racemic O-methyljoubertiamine Tetrahedron Letters. 19: 4229-4232. DOI: 10.1016/S0040-4039(01)95188-3 |
0.314 |
|
1978 |
Martin SF, Desai SR. Heteroatom-substituted butadienylphosphonium salts as reagents. A new synthesis of 2-ethoxycyclohexadienes and cyclohexenones The Journal of Organic Chemistry. 43: 4673-4675. DOI: 10.1002/Chin.197915189 |
0.456 |
|
1978 |
Martin SF, Phillips GW. Homologation-alkylation of carbonyl compounds via regiospecifically generated metallo enamines The Journal of Organic Chemistry. 43: 3792-3794. DOI: 10.1002/Chin.197905164 |
0.323 |
|
1978 |
MARTIN SF, CHOU T. ChemInform Abstract: STEREOSELECTIVE TOTAL SYNTHESIS OF RACEMIC ACORONE Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197838302 |
0.353 |
|
1978 |
Martin SF, Chou T. Stereoselective total synthesis of racemic acorone The Journal of Organic Chemistry. 43: 1027-1031. DOI: 10.1002/Chin.197838302 |
0.463 |
|
1977 |
Martin SF, Chou T, Payne CW. Carbonyl homologation with .alpha. substitution. A new synthesis of 4,4-disubstituted 2-cyclopentenones The Journal of Organic Chemistry. 42: 2520-2523. DOI: 10.1021/Jo00434A043 |
0.361 |
|
1977 |
Martin SF, DuPriest T. Reactions of allylpyrrolidine carbanions with electrophiles. A new homoenolate equivalent Tetrahedron Letters. 18: 3925-3928. DOI: 10.1016/S0040-4039(01)83392-X |
0.356 |
|
1977 |
MARTIN SF, CHOU T, PAYNE CW. ChemInform Abstract: CARBONYL HOMOLOGATION WITH α SUBSTITUTION. A NEW SYNTHESIS OF 4,4-DISUBSTITUTED 2-CYCLOPENTENONES Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/Chin.197743127 |
0.395 |
|
1977 |
MARTIN SF. ChemInform Abstract: CARBONYL HOMOLOGATION WITH α SUBSTITUTION. A NEW APPROACH TO SPIROANNELATION Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/Chin.197703162 |
0.314 |
|
1975 |
TAYLOR EC, MARTIN SF. ChemInform Abstract: A GENERAL METHOD FOR ALKYLATION AND ALKENYLATION OF HETEROCYCLES Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197511170 |
0.517 |
|
1974 |
Martin SF, Gompper R. Facile method for the transformation of ketones into .alpha.-substituted aldehydes The Journal of Organic Chemistry. 39: 2814-2815. DOI: 10.1021/Jo00932A036 |
0.582 |
|
1974 |
Taylor E, Martin S. A General Method of Alkylation and Alkenylation Heterocycles Journal of the American Chemical Society. 96: 8095-8102. DOI: 10.1021/Ja00833A601 |
0.505 |
|
1974 |
TAYLOR EC, CHITTENDEN ML, MARTIN SF. ChemInform Abstract: A GENERAL PROCEDURE FOR THE SYNTHESIS OF EPOXY-ALKYLATED AND ACYLATED HETEROCYCLES Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/Chin.197435298 |
0.579 |
|
1973 |
Taylor EC, Martin SF, Maki Y, Beardsley GP. Pteridines. XXVII. A New Synthetic Route to Pteridines and 7-Azapteridines Journal of Organic Chemistry. 38: 2238-2240. DOI: 10.1021/Jo00952A028 |
0.498 |
|
1973 |
TAYLOR EC, MARTIN SF, MAKI Y, BEARDSLEY GP. ChemInform Abstract: PTERIDINES PART 27, A NEW SYNTHETIC ROUTE TO PTERIDINES AND 7-AZAPTERIDINES Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197339280 |
0.511 |
|
1972 |
Taylor EC, Martin SF. A facile synthesis of quinine and related cinchona alkaloids. Journal of the American Chemical Society. 94: 6218-20. PMID 5054415 DOI: 10.1021/Ja00772A062 |
0.566 |
|
1972 |
Taylor EC, Martin SF. Synthesis of some 7-aryl-6-azapteridines from 1,2,4-triazine intermediates The Journal of Organic Chemistry. 37: 3958-3960. DOI: 10.1021/Jo00797A048 |
0.634 |
|
1972 |
Taylor EC, Martin SF. Facile method for alkylation and alkenylation of heterocycles Journal of the American Chemical Society. 94: 2874-2875. DOI: 10.1021/Ja00763A064 |
0.516 |
|
1972 |
TAYLOR EC, MARTIN SF. ChemInform Abstract: EINFACHE SYNTH. VON CHININ UND VERWANDTEN CINCHONAALKALOIDEN Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197245423 |
0.457 |
|
1972 |
TAYLOR EC, MARTIN SF. ChemInform Abstract: EINFACHE METHODE ZUR ALKYLIERUNG UND ALKENYLIERUNG VON HETEROCYCLEN Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197228152 |
0.435 |
|
1970 |
Taylor EC, Martin SF. Synthesis of as-triazines and pyrimido[4,5-e]-as-triazines (6-azapteridines) The Journal of Organic Chemistry. 35: 3792-3795. DOI: 10.1021/Jo00836A046 |
0.517 |
|
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