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Andrew G. Myers - Publications

Affiliations: 
Harvard University, Cambridge, MA, United States 
Area:
synthesis of natural products
Website:
http://www.chem.harvard.edu/groups/myers/page5/page5.html

189 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Mason JD, Terwilliger DW, Pote AR, Myers AG. Practical Gram-Scale Synthesis of Iboxamycin, a Potent Antibiotic Candidate. Journal of the American Chemical Society. PMID 34264649 DOI: 10.1021/jacs.1c03529  0.37
2021 Mitcheltree MJ, Stevenson JW, Pisipati A, Myers AG. A Practical, Component-Based Synthetic Route to Methylthiolincosamine Permitting Facile Northern-Half Diversification of Lincosamide Antibiotics. Journal of the American Chemical Society. PMID 33930268 DOI: 10.1021/jacs.1c03536  0.736
2017 Hogan PC, Chen CL, Mulvihill KM, Lawrence JF, Moorhead E, Rickmeier J, Myers AG. Large-scale preparation of key building blocks for the manufacture of fully synthetic macrolide antibiotics. The Journal of Antibiotics. PMID 29018266 DOI: 10.1038/Ja.2017.116  0.665
2016 Liu F, Wright PM, Myers AG. Diastereoselective Michael-Claisen Cyclizations of γ-Oxa-α,β-unsaturated Ketones en Route to 5-Oxatetracyclines. Organic Letters. PMID 27996275 DOI: 10.1021/Acs.Orglett.6B03491  0.373
2016 Seiple IB, Zhang Z, Jakubec P, Langlois-Mercier A, Wright PM, Hog DT, Yabu K, Allu SR, Fukuzaki T, Carlsen PN, Kitamura Y, Zhou X, Condakes ML, Szczypiński FT, Green WD, ... Myers AG, et al. A platform for the discovery of new macrolide antibiotics. Nature. 533: 338-45. PMID 27193679 DOI: 10.1038/Nature17967  0.783
2016 Liu F, Myers AG. Development of a platform for the discovery and practical synthesis of new tetracycline antibiotics. Current Opinion in Chemical Biology. 32: 48-57. PMID 27043373 DOI: 10.1016/J.Cbpa.2016.03.011  0.325
2015 Zhang Z, Fukuzaki T, Myers AG. Synthesis of D-Desosamine and Analogs by Rapid Assembly of 3-Amino Sugars. Angewandte Chemie (International Ed. in English). PMID 26612347 DOI: 10.1002/Anie.201507357  0.414
2015 Pelish HE, Liau BB, Nitulescu II, Tangpeerachaikul A, Poss ZC, Da Silva DH, Caruso BT, Arefolov A, Fadeyi O, Christie AL, Du K, Banka D, Schneider EV, Jestel A, Zou G, ... ... Myers AG, et al. Mediator kinase inhibition further activates super-enhancer-associated genes in AML. Nature. 526: 273-6. PMID 26416749 DOI: 10.1038/Nature14904  0.752
2015 Seiple IB, Hog DT, Myers AG. Practical Protocols for the Preparation of Highly Enantioenriched Silyl Ethers of (R)-3-Hydroxypentan-2-one, Building Blocks for the Synthesis of Macrolide Antibiotics Synlett. DOI: 10.1055/S-0035-1560972  0.691
2015 Zhang Z, Kitamura Y, Myers AG. An Efficient Directed Claisen Reaction Allows for Rapid Construction of 5,6-Disubstituted 1,3-Dioxin-4-ones Synthesis (Germany). 47: 2709-2712. DOI: 10.1055/S-0034-1378822  0.452
2014 Pröpper K, Dittrich B, Smaltz DJ, Magauer T, Myers AG. Crystalline guanine adducts of natural and synthetic trioxacarcins suggest a common biological mechanism and reveal a basis for the instability of trioxacarcin A. Bioorganic & Medicinal Chemistry Letters. 24: 4410-3. PMID 25176186 DOI: 10.1016/J.Bmcl.2014.08.016  0.794
2014 Wright PM, Seiple IB, Myers AG. The evolving role of chemical synthesis in antibacterial drug discovery. Angewandte Chemie (International Ed. in English). 53: 8840-69. PMID 24990531 DOI: 10.1002/Anie.201310843  0.675
2014 Seiple IB, Mercer JA, Sussman RJ, Zhang Z, Myers AG. Stereocontrolled synthesis of syn-β-Hydroxy-α-amino acids by direct aldolization of pseudoephenamine glycinamide. Angewandte Chemie (International Ed. in English). 53: 4642-7. PMID 24692320 DOI: 10.1002/Anie.201400928  0.748
2014 Magauer T, Smaltz DJ, Myers AG. Component-based syntheses of trioxacarcin a, DC-45-A1 and structural analogues Synlett. 25: A19-A22. DOI: 10.1055/s-0033-1340522  0.764
2014 Wright PM, Seiple IB, Myers AG. ChemInform Abstract: The Evolving Role of Chemical Synthesis in Antibacterial Drug Discovery Cheminform. 45: no-no. DOI: 10.1002/chin.201446263  0.649
2014 Seiple IB, Mercer JAM, Sussman RJ, Zhang Z, Myers AG. ChemInform Abstract: Stereocontrolled Synthesis of syn-β-Hydroxy-α-amino Acids by Direct Aldolization of Pseudoephenamine Glycinamide. Cheminform. 45: no-no. DOI: 10.1002/chin.201443029  0.694
2014 Wright PM, Seiple IB, Myers AG. Zur Rolle der chemischen Synthese in der Entwicklung antibakterieller Wirkstoffe Angewandte Chemie. 126: 8984-9014. DOI: 10.1002/Ange.201310843  0.627
2013 Blasdel LK, Lee D, Sun B, Myers AG. (S)-4-Trimethylsilyl-3-butyn-2-ol as an auxiliary for stereocontrolled synthesis of salinosporamide analogs with modifications at positions C2 and C5. Bioorganic & Medicinal Chemistry Letters. 23: 6905-10. PMID 24269479 DOI: 10.1016/J.Bmcl.2013.09.066  0.819
2013 Mellem KT, Myers AG. A simple, scalable synthetic route to (+)- and (-)-pseudoephenamine. Organic Letters. 15: 5594-7. PMID 24138164 DOI: 10.1021/Ol402815D  0.833
2013 Magauer T, Smaltz DJ, Myers AG. Component-based syntheses of trioxacarcin A, DC-45-A1 and structural analogues. Nature Chemistry. 5: 886-93. PMID 24056347 DOI: 10.1038/Nchem.1746  0.792
2013 Hugelshofer CL, Mellem KT, Myers AG. Synthesis of quaternary α-methyl α-amino acids by asymmetric alkylation of pseudoephenamine alaninamide pivaldimine. Organic Letters. 15: 3134-7. PMID 23746325 DOI: 10.1021/Ol401337P  0.822
2012 Morales MR, Mellem KT, Myers AG. Pseudoephenamine: a practical chiral auxiliary for asymmetric synthesis. Angewandte Chemie (International Ed. in English). 51: 4568-71. PMID 22461381 DOI: 10.1002/Anie.201200370  0.829
2012 Smaltz DJ, Švenda J, Myers AG. Diastereoselective additions of allylmetal reagents to free and protected syn-α,β-dihydroxyketones enable efficient synthetic routes to methyl trioxacarcinoside A. Organic Letters. 14: 1812-5. PMID 22404560 DOI: 10.1021/Ol300377A  0.817
2012 Morales MR, Mellem KT, Myers AG. ChemInform Abstract: Pseudoephenamine: A Practical Chiral Auxiliary for Asymmetric Synthesis. Cheminform. 43: no-no. DOI: 10.1002/chin.201238022  0.817
2012 Si C, Myers AG. ChemInform Abstract: A Versatile Synthesis of Substituted Isoquinolines. Cheminform. 43: no-no. DOI: 10.1002/chin.201211131  0.834
2011 Wright PM, Myers AG. Methodological Advances Permit the Stereocontrolled Construction of Diverse Fully Synthetic Tetracyclines Containing an All-Carbon Quaternary Center at Position C5a. Tetrahedron. 67: 9853-9869. PMID 22102762 DOI: 10.1016/J.Tet.2011.09.143  0.412
2011 Magauer T, Myers AG. Short and efficient synthetic route to methyl α-trioxacarcinoside B and anomerically activated derivatives. Organic Letters. 13: 5584-7. PMID 21958151 DOI: 10.1021/Ol202315M  0.674
2011 Kummer DA, Li D, Dion A, Myers AG. A practical, convergent route to the key precursor to the tetracycline antibiotics. Chemical Science (Royal Society of Chemistry : 2010). 2: 1710-1718. PMID 21949588 DOI: 10.1039/C1Sc00303H  0.466
2011 Si C, Myers AG. A versatile synthesis of substituted isoquinolines. Angewandte Chemie (International Ed. in English). 50: 10409-13. PMID 21910199 DOI: 10.1002/Anie.201104769  0.832
2011 Smaltz DJ, Myers AG. Scalable synthesis of enantiomerically pure syn-2,3-dihydroxybutyrate by Sharpless asymmetric dihydroxylation of p-phenylbenzyl crotonate. The Journal of Organic Chemistry. 76: 8554-9. PMID 21895005 DOI: 10.1021/Jo2016746  0.81
2011 Simmons RL, Yu RT, Myers AG. Storable arylpalladium(II) reagents for alkene labeling in aqueous media. Journal of the American Chemical Society. 133: 15870-3. PMID 21888420 DOI: 10.1021/Ja206339S  0.608
2011 Švenda J, Hill N, Myers AG. A multiply convergent platform for the synthesis of trioxacarcins. Proceedings of the National Academy of Sciences of the United States of America. 108: 6709-14. PMID 21245350 DOI: 10.1073/Pnas.1015257108  0.8
2010 Flyer AN, Si C, Myers AG. Synthesis of cortistatins A, J, K and L. Nature Chemistry. 2: 886-92. PMID 20861906 DOI: 10.1055/S-0030-1259131  0.794
2010 Myers AG, Glatthar R, Hammond M, Harrington PM, Kuo EY, Liang J, Schaus SE, Wu Y, Xiang J. ChemInform Abstract: Development of an Enantioselective Synthetic Route to Neocarzinostatin Chromophore and Its Use for Multiple Radioisotopic Incorporation. Cheminform. 33: no-no. DOI: 10.1002/chin.200236229  0.619
2010 Myers AG, Siegel DR, Buzard DJ, Charest MG. ChemInform Abstract: Synthesis of a Broad Array of Highly Functionalized, Enantiomerically Pure Cyclohexanecarboxylic Acid Derivatives by Microbial Dihydroxylation of Benzoic Acid and Subsequent Oxidative and Rearrangement Reactions. Cheminform. 33: no-no. DOI: 10.1002/chin.200202111  0.819
2010 Myers AG, Zhong B, Movassaghi M, Kung DW, Lanman BA, Kwon S. ChemInform Abstract: Synthesis of Highly Epimerizable N-Protected α-Amino Aldehydes of High Enantiomeric Excess. Cheminform. 31: no-no. DOI: 10.1002/chin.200020061  0.816
2010 Myers AG, Kung DW, Zhong B, Movassaghi M, Kwon S. ChemInform Abstract: Preparation of Chiral, C-Protected α-Amino Aldehydes of High Optical Purity and Their Use as Condensation Components in a Linear Synthesis Strategy. Cheminform. 31: no-no. DOI: 10.1002/chin.200002109  0.816
2010 Myers AG, Schnider P, Kwon S, Kung DW. ChemInform Abstract: Greatly Simplified Procedures for the Synthesis of α-Amino Acids by the Direct Alkylation of Pseudoephedrine Glycinamide Hydrate. Cheminform. 30: no-no. DOI: 10.1002/chin.199937215  0.767
2010 Myers AG, Goldberg SD. ChemInform Abstract: Concise Synthesis of the Bicyclic Core of the Chromoprotein Antibiotics Kedarcidin and Neocarzinostatin by Transannular Reductive Cyclization of a Tetrayne Precursor. Cheminform. 30: no-no. DOI: 10.1002/chin.199912243  0.683
2010 MYERS AG, MOVASSAGHI M. ChemInform Abstract: Highly Efficient Methodology for the Reductive Coupling of Aldehyde Tosylhydrazones with Alkyllithium Reagents. Cheminform. 30: no-no. DOI: 10.1002/chin.199903040  0.568
2010 MYERS AG, LIANG J, HAMMOND M, HARRINGTON PM, WU Y, KUO EY. ChemInform Abstract: Total Synthesis of (+)-Neocarzinostatin Chromophore. Cheminform. 29: no-no. DOI: 10.1002/chin.199840266  0.332
2010 MYERS AG, MCKINSTRY L, BARBAY JK, GLEASON JL. ChemInform Abstract: Practical Methodology for the Asymmetric Synthesis of Organofluorine Compounds. Cheminform. 29: no-no. DOI: 10.1002/chin.199821071  0.79
2010 MYERS AG, ZHENG B, MOVASSAGHI M. ChemInform Abstract: Preparation of the Reagent o-Nitrobenzenesulfonylhydrazide. Cheminform. 29: no-no. DOI: 10.1002/chin.199811110  0.507
2010 MYERS AG, MOVASSAGHI M, ZHENG B. ChemInform Abstract: Single-Step Process for the Reductive Deoxygenation of Unhindered Alcohols. Cheminform. 28: no-no. DOI: 10.1002/chin.199750063  0.513
2010 MYERS AG, MOVASSAGHI M, ZHENG B. ChemInform Abstract: Mechanistic Studies of the Free-Radical Fragmentation of Monoalkyl Diazenes. Cheminform. 28: no-no. DOI: 10.1002/chin.199749019  0.491
2010 MYERS AG, YANG BH, CHEN H, MCKINSTRY L, KOPECKY DJ, GLEASON JL. ChemInform Abstract: Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones Cheminform. 28: no-no. DOI: 10.1002/chin.199746041  0.318
2010 MYERS AG, HORIGUCHI Y. ChemInform Abstract: Synthesis of the Naphthoic Acid Component of Kedarcidin Chromophore by Routes Employing Photochemical and Thermal Electrocyclic Ring Closure Reactions. Cheminform. 28: no-no. DOI: 10.1002/chin.199738140  0.319
2010 MYERS AG, GLEASON JL, YOON T, KUNG DW. ChemInform Abstract: Highly Practical Methodology for the Synthesis of D- and L-α- Amino Acids, N-Protected α-Amino Acids, and N-Methyl-α- amino Acids. Cheminform. 28: no-no. DOI: 10.1002/chin.199719219  0.7
2010 MYERS AG, HAMMOND M, WU Y, XIANG J, HARRINGTON PM, KUO EY. ChemInform Abstract: Enantioselective Synthesis of Neocarzinostatin Chromophore Aglycon ( VII). Cheminform. 28: no-no. DOI: 10.1002/chin.199707267  0.373
2010 MYERS AG, MCKINSTRY L. ChemInform Abstract: Practical Syntheses of Enantiomerically Enriched γ-Lactones and . gamma.-Hydroxy Ketones by the Alkylation of Pseudoephedrine Amides with Epoxides and Their Derivatives. Cheminform. 27: no-no. DOI: 10.1002/chin.199634019  0.332
2010 MYERS AG, YOON T, GLEASON JL. ChemInform Abstract: A One-Step Synthesis of Pseudoephedrine Glycinamide, a Versatile Precursor for the Synthesis of α-Amino Acids. Cheminform. 26: no-no. DOI: 10.1002/chin.199540215  0.377
2010 MYERS AG, CONDROSKI KR. ChemInform Abstract: Synthesis of (.+-.)-7,8-Epoxy-4-basmen-6-one by Transannular Cyclization Strategy. Cheminform. 26: no-no. DOI: 10.1002/chin.199531200  0.349
2010 MYERS AG, FRALEY ME, TOM NJ. ChemInform Abstract: Highly Convergent Route to Dynemicins of Wide Structural Variability. Enantioselective Synthesis of Quinone Imine Precursors to Natural and Nonnatural Dynemicins. Cheminform. 26: no-no. DOI: 10.1002/chin.199521285  0.313
2010 MYERS AG, YANG BH, CHEN H, GLEASON JL. ChemInform Abstract: Use of Pseudoephedrine as a Practical Chiral Auxiliary for Asymmetric Synthesis. Cheminform. 26: no-no. DOI: 10.1002/chin.199517025  0.302
2010 MYERS AG, GIN DY, ROGERS DH. ChemInform Abstract: Synthetic Studies of the Tunicamycin Antibiotics. Preparation of (+)- Tunicaminyluracil, (+)-Tunicamycin-V, and 5′-epi-Tunicamycin-V. Cheminform. 25: no-no. DOI: 10.1002/chin.199446258  0.716
2010 MYERS AG, GIN DY, ROGERS DH. ChemInform Abstract: A Convergent Synthetic Route to the Tunicamycin Antibiotics. Synthesis of (+)-Tunicamycin V. Cheminform. 24: no-no. DOI: 10.1002/chin.199330291  0.758
2010 MYERS AG, FINNEY NS. ChemInform Abstract: Synthesis of 1,6-Didehydro(10)annulene. Observation of Its Exceptionally Facile Rearrangement to Form the Biradical 1,5- Dehydronaphthalene. Cheminform. 24: no-no. DOI: 10.1002/chin.199318174  0.693
2010 MYERS AG, GIN DY, WIDDOWSON KL. ChemInform Abstract: Silicon-Mediated Reductive Coupling of Aldehydes and Allylic Alcohols. A Stereoselective Synthesis of Tunicaminyluracil. Cheminform. 23: no-no. DOI: 10.1002/chin.199215292  0.751
2010 MYERS AG, HARRINGTON PM, KUO EY. ChemInform Abstract: Enantioselective Synthesis of the Epoxy Diyne Core (VII) of Neocarzinostatin Chromophore. Cheminform. 22: no-no. DOI: 10.1002/chin.199121280  0.335
2010 MYERS AG, WIDDOWSON KL. ChemInform Abstract: A Silicon-Directed Aldol Condensation. Synthesis of Enantiomerically Pure Anti Aldols. Cheminform. 22: no-no. DOI: 10.1002/chin.199113076  0.3
2010 MYERS AG, KUKKOLA PJ. ChemInform Abstract: Stereoselective Synthesis of Olefins from Silylated Sulfonylhydrazones. Cheminform. 22: no-no. DOI: 10.1002/chin.199106073  0.388
2009 Svenda J, Myers AG. Anti-selective epoxidation of methyl alpha-methylene-beta-tert-butyldimethylsilyloxycarboxylate esters. Evidence for stereospecific oxygen atom transfer in a nucleophilic epoxidation process. Organic Letters. 11: 2437-40. PMID 19397300 DOI: 10.1021/Ol900665A  0.752
2009 Lim SM, Hill N, Myers AG. A method for the preparation of differentiated trans-1,2-diol derivatives with enantio- and diastereocontrol. Journal of the American Chemical Society. 131: 5763-5. PMID 19341239 DOI: 10.1021/Ja901283Q  0.633
2009 Kummer DA, Chain WJ, Morales MR, Quiroga O, Myers AG. ChemInform Abstract: Stereocontrolled Alkylative Construction of Quaternary Carbon Centers. Cheminform. 40. DOI: 10.1002/chin.200907027  0.709
2008 Sun C, Wang Q, Brubaker JD, Wright PM, Lerner CD, Noson K, Charest M, Siegel DR, Wang YM, Myers AG. A robust platform for the synthesis of new tetracycline antibiotics. Journal of the American Chemical Society. 130: 17913-27. PMID 19053822 DOI: 10.1021/Ja806629E  0.8
2008 Kummer DA, Chain WJ, Morales MR, Quiroga O, Myers AG. Stereocontrolled alkylative construction of quaternary carbon centers. Journal of the American Chemical Society. 130: 13231-3. PMID 18788739 DOI: 10.1021/Ja806021Y  0.741
2007 Wulff JE, Siegrist R, Myers AG. The natural product avrainvillamide binds to the oncoprotein nucleophosmin. Journal of the American Chemical Society. 129: 14444-51. PMID 17958425 DOI: 10.1021/Ja075327F  0.636
2007 Brubaker JD, Myers AG. A practical, enantioselective synthetic route to a key precursor to the tetracycline antibiotics. Organic Letters. 9: 3523-5. PMID 17691796 DOI: 10.1021/Ol071377D  0.783
2007 Ren F, Hogan PC, Anderson AJ, Myers AG. Synthesis of L-kedarosamine in protected form and its efficient incorporation into an advanced intermediate to kedarcidin chromophore. Organic Letters. 9: 1923-5. PMID 17439225 DOI: 10.1021/Ol070450X  0.747
2007 Ren F, Hogan PC, Anderson AJ, Myers AG. Kedarcidin chromophore: synthesis of its proposed structure and evidence for a stereochemical revision. Journal of the American Chemical Society. 129: 5381-3. PMID 17417855 DOI: 10.1021/Ja071205B  0.755
2007 Wulff JE, Herzon SB, Siegrist R, Myers AG. Evidence for the rapid conversion of stephacidin B into the electrophilic monomer avrainvillamide in cell culture. Journal of the American Chemical Society. 129: 4898-9. PMID 17397160 DOI: 10.1021/Ja0690971  0.727
2007 Chain WJ, Myers AG. A convenient, NMR-based method for the analysis of diastereomeric mixtures of pseudoephedrine amides. Organic Letters. 9: 355-7. PMID 17217303 DOI: 10.1021/Ol0628762  0.772
2007 Myers A, Ji N, O’Dowd H, Rosen B. Synthesis of N1999A2 Synfacts. 2007: 0343-0343. DOI: 10.1055/S-2007-968289  0.54
2006 Dineen TA, Zajac MA, Myers AG. Efficient transamidation of primary carboxamides by in situ activation with N,N-dialkylformamide dimethyl acetals. Journal of the American Chemical Society. 128: 16406-9. PMID 17165798 DOI: 10.1021/Ja066728I  0.788
2006 Ji N, O'Dowd H, Rosen BM, Myers AG. Enantioselective synthesis of N1999A2. Journal of the American Chemical Society. 128: 14825-7. PMID 17105291 DOI: 10.1021/Ja0662467  0.625
2006 Myers A, Kwon S. Synthesis of (-)-Quinocarcin Synfacts. 2006: 0411-0411. DOI: 10.1055/S-2006-934399  0.445
2005 Kwon S, Myers AG. Synthesis of (-)-quinocarcin by directed condensation of alpha-amino aldehydes. Journal of the American Chemical Society. 127: 16796-7. PMID 16316220 DOI: 10.1021/Ja056206N  0.628
2005 Blasdel LK, Myers AG. Use of lithium hexafluoroisopropoxide as a mild base for Horner-Wadsworth-Emmons olefination of epimerizable aldehydes. Organic Letters. 7: 4281-3. PMID 16146407 DOI: 10.1021/Ol051785M  0.805
2005 Tanaka D, Romeril SP, Myers AG. On the mechanism of the palladium(II)-catalyzed decarboxylative olefination of arene carboxylic acids. Crystallographic characterization of non-phosphine palladium(II) intermediates and observation of their stepwise transformation in Heck-like processes. Journal of the American Chemical Society. 127: 10323-33. PMID 16028944 DOI: 10.1021/Ja052099L  0.331
2005 Charest MG, Siegel DR, Myers AG. Synthesis of (-)-tetracycline. Journal of the American Chemical Society. 127: 8292-3. PMID 15941256 DOI: 10.1021/Ja052151D  0.829
2005 Charest MG, Lerner CD, Brubaker JD, Siegel DR, Myers AG. A convergent enantioselective route to structurally diverse 6-deoxytetracycline antibiotics. Science (New York, N.Y.). 308: 395-8. PMID 15831754 DOI: 10.1126/Science.1109755  0.811
2005 Herzon SB, Myers AG. Enantioselective synthesis of stephacidin B. Journal of the American Chemical Society. 127: 5342-4. PMID 15826171 DOI: 10.1021/Ja0510616  0.688
2004 Ji N, Rosen BM, Myers AG. Method for the rapid synthesis of highly functionalized 2-hydroxy-1-naphthoates. Syntheses of the naphthoic acid components of neocarzinostatin chromophore and N1999A2. Organic Letters. 6: 4551-3. PMID 15548073 DOI: 10.1021/Ol048075L  0.632
2004 Furrow ME, Myers AG. A general procedure for the esterification of carboxylic acids with diazoalkanes generated in situ by the oxidation of N-tert-butyldimethylsilylhydrazones with (difluoroiodo)benzene. Journal of the American Chemical Society. 126: 12222-3. PMID 15453728 DOI: 10.1021/Ja0459779  0.815
2004 Haidle AM, Myers AG. An enantioselective, modular, and general route to the cytochalasins: synthesis of L-696,474 and cytochalasin B. Proceedings of the National Academy of Sciences of the United States of America. 101: 12048-53. PMID 15208404 DOI: 10.1073/Pnas.0402111101  0.787
2004 Furrow ME, Myers AG. Practical procedures for the preparation of N-tert-butyldimethylsilylhydrazones and their use in modified Wolff-Kishner reductions and in the synthesis of vinyl halides and gem-dihalides. Journal of the American Chemical Society. 126: 5436-45. PMID 15113215 DOI: 10.1021/Ja049694S  0.834
2004 Xing C, LaPorte JR, Barbay JK, Myers AG. Identification of GAPDH as a protein target of the saframycin antiproliferative agents. Proceedings of the National Academy of Sciences of the United States of America. 101: 5862-6. PMID 15079082 DOI: 10.1073/Pnas.0307476101  0.769
2004 Myers AG, Sogi M, Lewis MA, Arvedson SP. Synthetic and theoretical studies of cyclobuta[1,2:3,4]dicyclopentene. Organocobalt intermediates in the construction of the unsaturated carbon skeleton and their transformation into novel cobaltacyclic complexes by C-C insertion. The Journal of Organic Chemistry. 69: 2516-25. PMID 15049653 DOI: 10.1021/Jo030368P  0.804
2004 Lanman BA, Myers AG. Efficient, stereoselective synthesis of trans-2,5-disubstituted morpholines. Organic Letters. 6: 1045-7. PMID 15012096 DOI: 10.1021/Ol049861T  0.766
2004 Tanaka D, Myers AG. Heck-type arylation of 2-cycloalken-1-ones with arylpalladium intermediates formed by decarboxylative palladation and by aryl iodide insertion. Organic Letters. 6: 433-6. PMID 14748611 DOI: 10.1021/Ol0363467  0.411
2003 Myers AG, Herzon SB. Identification of a novel Michael acceptor group for the reversible addition of oxygen- and sulfur-based nucleophiles. Synthesis and reactivity of the 3-alkylidene-3H-indole 1-oxide function of avrainvillamide. Journal of the American Chemical Society. 125: 12080-1. PMID 14518979 DOI: 10.1021/Ja0372006  0.619
2003 Myers AG, Zheng B. (tert‐Butyldimethylsilyl)Allene Organic Syntheses. 76: 178-178. DOI: 10.1002/0471264180.Os076.18  0.369
2003 Myers AG, Gleason JL. Asymmetric Synthesis of α‐Amino Acids by the Alkylation of Pseudoephedrine Glycinamide: L‐Allylglycine and N‐Boc‐L‐Allylglycine Organic Syntheses. 76: 57-57. DOI: 10.1002/0471264180.Os076.07  0.678
2003 Myers AG, Dragovich PS. Synthesis of Functionalized Enynes by Palladium/Copper‐Catalyzed Coupling Reactions of Acetylenes with (Z)‐2,3‐Dibromopropenoic acid Ethyl Ester: (Z)‐2‐Bromo‐5‐(Trimethylsilyl)‐2‐Penten‐4‐ynoic Acid Ethyl Ester Organic Syntheses. 104-104. DOI: 10.1002/0471264180.Os072.13  0.43
2002 Myers AG, Hogan PC, Hurd AR, Goldberg SD. Enantioselective synthesis of kedarcidin chromophore aglycon in differentially protected form. Angewandte Chemie (International Ed. in English). 41: 1062-7. PMID 12491313 DOI: 10.1002/1521-3773(20020315)41:6<1062::Aid-Anie1062>3.0.Co;2-8  0.806
2002 Myers AG, Lanman BA. A solid-supported, enantioselective synthesis suitable for the rapid preparation of large numbers of diverse structural analogues of (-)-saframycin A. Journal of the American Chemical Society. 124: 12969-71. PMID 12405822 DOI: 10.1021/Ja027729N  0.773
2002 Myers AG, Tanaka D, Mannion MR. Development of a decarboxylative palladation reaction and its use in a Heck-type olefination of arene carboxylates. Journal of the American Chemical Society. 124: 11250-1. PMID 12236722 DOI: 10.1021/Ja027523M  0.349
2002 Plowright AT, Schaus SE, Myers AG. Transcriptional response pathways in a yeast strain sensitive to saframycin a and a more potent analog: evidence for a common basis of activity. Chemistry & Biology. 9: 607-18. PMID 12031667 DOI: 10.1016/S1074-5521(02)00137-0  0.579
2002 Myers AG, Glatthar R, Hammond M, Harrington PM, Kuo EY, Liang J, Schaus SE, Wu Y, Xiang JN. Development of an enantioselective synthetic route to neocarzinostatin chromophore and its use for multiple radioisotopic incorporation. Journal of the American Chemical Society. 124: 5380-401. PMID 11996579 DOI: 10.1021/Ja012487X  0.748
2002 Myers AG, Hurd AR, Hogan PC. Evidence for facile atropisomerism and simple (non-nucleophilic) biradical-forming cycloaromatization within kedarcidin chromophore aglycon. Journal of the American Chemical Society. 124: 4583-5. PMID 11971704 DOI: 10.1021/Ja020152P  0.698
2002 Myers AG, Siu M, Ren F. Enantioselective synthesis of (-)-terpestacin and (-)-fusaproliferin: clarification of optical rotational measurements and absolute configurational assignments establishes a homochiral structural series. Journal of the American Chemical Society. 124: 4230-2. PMID 11960450 DOI: 10.1021/Ja020072L  0.71
2002 Myers AG, Siu M. Lewis acid mediated control of allylic epoxide opening in carbocyclization and halide addition pathways Tetrahedron. 58: 6397-6404. DOI: 10.1016/S0040-4020(02)00653-1  0.669
2001 Schaus SE, Cavalieri D, Myers AG. Gene transcription analysis of Saccharomyces cerevisiae exposed to neocarzinostatin protein-chromophore complex reveals evidence of DNA damage, a potential mechanism of resistance, and consequences of prolonged exposure. Proceedings of the National Academy of Sciences of the United States of America. 98: 11075-80. PMID 11562456 DOI: 10.1073/Pnas.191340698  0.579
2001 Myers AG, Siegel DR, Buzard DJ, Charest MG. Synthesis of a broad array of highly functionalized, enantiomerically pure cyclohexanecarboxylic acid derivatives by microbial dihydroxylation of benzoic acid and subsequent oxidative and rearrangement reactions. Organic Letters. 3: 2923-6. PMID 11529791 DOI: 10.1021/Ol010151M  0.814
2001 Myers AG, Barbay JK, Zhong B. Asymmetric synthesis of chiral organofluorine compounds: use of nonracemic fluoroiodoacetic acid as a practical electrophile and its application to the synthesis of monofluoro hydroxyethylene dipeptide isosteres within a novel series of HIV protease inhibitors. Journal of the American Chemical Society. 123: 7207-19. PMID 11472148 DOI: 10.1021/Ja010113Y  0.823
2001 Myers AG, Plowright AT. Synthesis and evaluation of bishydroquinone derivatives of (-)-saframycin A: identification of a versatile molecular template imparting potent antiproliferative activity. Journal of the American Chemical Society. 123: 5114-5. PMID 11457349 DOI: 10.1021/Ja0103086  0.369
2001 Myers AG, Barbay JK. On the inherent instability of alpha-amino alpha'-fluoro ketones. Evidence for their transformation to reactive oxyvinyliminium ion intermediates. Organic Letters. 3: 425-8. PMID 11428030 DOI: 10.1021/Ol006931X  0.787
2001 Myers AG, Zhong B, Kung DW, Movassaghi M, Lanman BA, Kwon S. ChemInform Abstract: Synthesis of C-Protected α-Amino Aldehydes of High Enantiomeric Excess from Highly Epimerizable N-Protected α-Amino Aldehydes. Cheminform. 32: no-no. DOI: 10.1002/chin.200108097  0.811
2000 Myers AG, Zhong B, Kung DW, Movassaghi M, Lanman BA, Kwon S. Synthesis of C-protected alpha-amino aldehydes of high enantiomeric excess from highly epimerizable N-protected alpha-amino aldehydes. Organic Letters. 2: 3337-40. PMID 11029204 DOI: 10.1021/Ol006427S  0.803
2000 Myers AG, Kung DW. One-step construction of the pentacyclic skeleton of saframycin A from a "Trimer" of alpha-amino aldehydes. Organic Letters. 2: 3019-22. PMID 10986097 DOI: 10.1021/Ol0063398  0.714
2000 Myers AG, Goldberg SD. Synthesis of the Kedarcidin Core Structure by a Transannular Cyclization Pathway Financial support from the National Institutes of Health is gratefully acknowledged. Angewandte Chemie (International Ed. in English). 39: 2732-2735. PMID 10934409 DOI: 10.1002/1521-3773(20000804)39:15<2732::Aid-Anie2732>3.0.Co;2-9  0.631
2000 Myers AG, Kung DW, Zhong B. Observations concerning the existence and reactivity of free α-amino aldehydes as chemical intermediates: Evidence for epimerization-free adduct formation with various nucleophiles [11] Journal of the American Chemical Society. 122: 3236-3237. DOI: 10.1021/Ja000136X  0.802
2000 Myers AG, Zhong B, Movassaghi M, Kung DW, Lanman BA, Kwon S. Synthesis of highly epimerizable N-protected α-amino aldehydes of high enantiomeric excess Tetrahedron Letters. 41: 1359-1362. DOI: 10.1016/S0040-4039(99)02293-5  0.807
2000 Myers AG, Yang BH, Chen H. Transformation of pseudoephedrine amides into highly enantiomerically enriched aldehydes, alcohols, and ketones Organic Syntheses. 77: 29-42. DOI: 10.1002/0471264180.Os077.04  0.376
2000 Myers AG, Yang BH. Synthesis and diastereoselective alkylation of pseudoephedrine amides Organic Syntheses. 77: 22-28. DOI: 10.1002/0471264180.Os077.03  0.424
2000 Myers AG, Kung DW. One-step construction of the pentacyclic skeleton of saframycin A from a "trimer" of α-amino aldehydes Organic Letters. 2: 3019-3022.  0.697
1999 Myers AG, Schnider P, Kwon S, Kung DW. Greatly Simplified Procedures for the Synthesis of alpha-Amino Acids by the Direct Alkylation of Pseudoephedrine Glycinamide Hydrate. The Journal of Organic Chemistry. 64: 3322-3327. PMID 11674437 DOI: 10.1021/Jo990341Z  0.783
1999 Myers AG, Schnider P, Kwon S, Kung DW. Greatly simplified procedures for the synthesis of α-amino acids by the direct alkylation of pseudoephedrine glycinamide hydrate Journal of Organic Chemistry. 64: 3322-3327. DOI: 10.1021/jo990341z  0.763
1999 Myers AG, Kung DW. A concise, stereocontrolled synthesis of (-)-saframycin A by the directed condensation of α-amino aldehyde precursors [1] Journal of the American Chemical Society. 121: 10828-10829. DOI: 10.1021/Ja993079K  0.752
1999 Myers AG, Kung DW, Zhong B, Movassaghi M, Kwon S. Preparation of chiral, C-protected α-amino aldehydes of high optical purity and their use as condensation components in a linear synthesis strategy Journal of the American Chemical Society. 121: 8401-8402. DOI: 10.1021/Ja9911824  0.817
1999 Myers AG, Liang J, Hammond M. Synthetic replacement of the methylamino group of neocarzinostatin chromophore with hydroxyl prohibits thiol activation in organic solvents and diminishes the rate and efficiency of thiol-promoted DNA cleavage in water Tetrahedron Letters. 40: 5129-5133. DOI: 10.1016/S0040-4039(99)00880-1  0.466
1998 Myers AG, Movassaghi M. Highly efficient methodology for the reductive coupling of aldehyde tosylhydrazones with alkyllithium reagents [4] Journal of the American Chemical Society. 120: 8891-8892. DOI: 10.1021/Ja981918H  0.668
1998 Myers AG, Liang J, Hammond M, Harrington PM, Wu Y, Kuo EY. Total synthesis of (+)-neocarzinostatin chromophore [3] Journal of the American Chemical Society. 120: 5319-5320. DOI: 10.1021/Ja980588Y  0.435
1998 Myers AG, Goldberg SD. Concise synthesis of the bicyclic core of the chromoprotein antibiotics kedarcidin and neocarzinostatin by transannular reductive cyclization of a tetrayne precursor Tetrahedron Letters. 39: 9633-9636. DOI: 10.1016/S0040-4039(98)02279-5  0.688
1998 Myers AG, McKinstry L, Barbay JK, Gleason JL. Practical methodology for the asymmetric synthesis of organofluorine compounds Tetrahedron Letters. 39: 1335-1338. DOI: 10.1016/S0040-4039(98)00152-X  0.827
1998 Lopez RM, Hays DS, Fu GC, Myers AG, Movassaghi M, Zheng B. Bu3SnH-catalyzed Barton-McCombie deoxygenation of alcohols: Single-step process for the reductive deoxygenation of unhindered alcohols Chemtracts. 11: 67-72.  0.501
1997 Myers AG, Zheng B, Movassaghi M. Preparation of the Reagent o-Nitrobenzenesulfonylhydrazide. The Journal of Organic Chemistry. 62: 7507. PMID 11671877 DOI: 10.1021/Jo9710137  0.608
1997 Myers AG, Yang BH, Chen H, Kopecky DJ. Asymmetric synthesis of 1,3-dialkyl-substituted carbon chains of any stereochemical configuration by an iterable process Synlett. 457-459. DOI: 10.1055/S-1997-6121  0.368
1997 Myers AG, Zheng B, Movassaghi M. Preparation of the reagent o-nitrobenzenesulfonylhydrazide Journal of Organic Chemistry. 62: 7507. DOI: 10.1021/jo9710137  0.492
1997 Myers AG, Movassaghi M, Zheng B. Single-step process for the reductive deoxygenation of unhindered alcohols Journal of the American Chemical Society. 119: 8572-8573. DOI: 10.1021/Ja971768V  0.551
1997 Myers AG, Yang BH, Chen H, McKinstry L, Kopecky DJ, Gleason JL. Pseudoephedrine as a practical chiral auxiliary for the synthesis of highly enantiomerically enriched carboxylic acids, alcohols, aldehydes, and ketones Journal of the American Chemical Society. 119: 6496-6511. DOI: 10.1021/Ja970402F  0.744
1997 Myers AG, Tom NJ, Fraley ME, Cohen SB, Madar DJ. A convergent synthetic route to (+)-dynemicin a and analogs of wide structural variability Journal of the American Chemical Society. 119: 6072-6094. DOI: 10.1021/Ja9703741  0.494
1997 Myers AG, Gleason JL, Yoon T, Kung DW. Highly practical methodology for the synthesis of D- and L-α-amino acids, N-protected α-amino acids, and N-methyl-α-amino acids Journal of the American Chemical Society. 119: 656-673. DOI: 10.1021/Ja9624073  0.824
1997 Myers AG, McKinstry L, Gleason JL. Synthesis of tertiary alkyl fluoride centers by asymmetric C-C(F) bond formation Tetrahedron Letters. 38: 7037-7040. DOI: 10.1016/S0040-4039(97)01706-1  0.723
1997 Myers AG, Movassaghi M, Zheng B. Mechanistic studies of the free-radical fragmentation of monoalkyl diazenes Tetrahedron Letters. 38: 6569-6572. DOI: 10.1016/S0040-4039(97)01497-4  0.572
1997 Myers AG, Horiguchi Y. Synthesis of the naphthoic acid component of kedarcidin chromophore by routes employing photochemical and thermal electrocyclic ring closure reactions Tetrahedron Letters. 38: 4363-4366. DOI: 10.1016/S0040-4039(97)00844-7  0.443
1996 Myers AG, Gleason JL. A Practical Synthesis of L-Azatyrosine. The Journal of Organic Chemistry. 61: 813-815. PMID 11667015 DOI: 10.1021/Jo9515079  0.604
1996 Myers AG, McKinstry L. Practical syntheses of enantiomerically enriched γ-lactones and γ-hydroxy ketones by the alkylation of pseudoephedrine amides with epoxides and their derivatives Journal of Organic Chemistry. 61: 2428-2440. DOI: 10.1021/Jo952032O  0.464
1996 Myers AG, Hammond M, Wu Y, Xiang JN, Harrington PM, Kuo EY. Enantioselective synthesis of neocarzinostatin chromophore aglycon Journal of the American Chemical Society. 118: 10006-10007. DOI: 10.1021/Ja9618863  0.354
1996 Myers AG, Zheng B. New and stereospecific synthesis of allenes in a single step from propargylic alcohols Journal of the American Chemical Society. 118: 4492-4493. DOI: 10.1021/Ja960443W  0.346
1996 Myers AG, Arvedson SP, Lee RW. A new and unusual pathway for the reaction of neocarzinostatin chromophore with thiols. Revised structure of the protein-directed thiol adduct Journal of the American Chemical Society. 118: 4725-4726. DOI: 10.1021/Ja960335+  0.359
1996 Myers AG, Zheng B. An efficient method for the reductive transposition of allylic alcohols Tetrahedron Letters. 37: 4841-4844. DOI: 10.1016/0040-4039(96)00965-3  0.353
1996 Myers AG, Yang BH, Kopecky DJ. Lithium amidotrihydroborate, a powerful new reductant. Transformation of tertiary amides to primary alcohols Tetrahedron Letters. 37: 3623-3626. DOI: 10.1016/0040-4039(96)00652-1  0.331
1996 Myers AG, Hammond M, Wu Y. An improved preparation of highly enantiomerically enriched (A)-(+)-4-tert-butyldimethylsiloxy-2-cyclopenten-1-one Tetrahedron Letters. 37: 3083-3086. DOI: 10.1016/0040-4039(96)00501-1  0.371
1996 Myers AG, Subramanian V, Hammond M. A concise synthesis of the naphthoic acid component of neocarzinostatin chromophore featuring a new photocyclization reaction Tetrahedron Letters. 37: 587-590. DOI: 10.1016/0040-4039(95)02268-6  0.454
1995 Myers AG, Fraley ME, Tom NJ, Cohen SB, Madar DJ. Synthesis of (+)-dynemicin A and analogs of wide structural variability: establishment of the absolute configuration of natural dynemicin A. Chemistry & Biology. 2: 33-43. PMID 9383401 DOI: 10.1016/1074-5521(95)90078-0  0.505
1995 Myers AG, Gleason JL, Yoon T. A practical method for the synthesis of D- or L-α-amino acids by the alkylation of (+)- or (-)-pseudoephedrine glycinamide Journal of the American Chemical Society. 117: 8488-8489. DOI: 10.1021/Ja00137A034  0.691
1995 Myers AG, Condroski KR. Synthesis of (.+-.)-7,8-Epoxy-4-basmen-6-one by a Transannular Cyclization Strategy Journal of the American Chemical Society. 117: 3057-3083. DOI: 10.1021/ja00116a012  0.336
1995 Myers AG, Yoon T. Synthesis of highly enantiomerically enriched N-Boc-α-amino ketones from pseudoephedrine N-Boc-α-amino acid amides Tetrahedron Letters. 36: 9429-9432. DOI: 10.1016/0040-4039(95)02053-5  0.411
1995 Myers AG, Yoon T, Gleason JL. A one-step synthesis of pseudoephedrine glycinamide, a versatile precursor for the synthesis of α-amino acids Tetrahedron Letters. 36: 4555-4558. DOI: 10.1016/0040-4039(95)00820-3  0.734
1994 Myers AG, Fraley ME, Tom NJ. Highly Convergent Route to Dynemicins of Wide Structural Variability. Enantioselective Synthesis of Quinone Imine Precursors to Natural and Nonnatural Dynemicins Journal of the American Chemical Society. 116: 11556-11557. DOI: 10.1021/Ja00104A041  0.421
1994 Myers AG, Yang BH, Chen H, Gleason JL. Use of Pseudoephedrine as a Practical Chiral Auxiliary for Asymmetric Synthesis Journal of the American Chemical Society. 116: 9361-9362. DOI: 10.1021/Ja00099A076  0.737
1994 Myers AG, Gin DY, Rogers DH. Synthetic Studies of the Tunicamycin Antibiotics. Preparation of (+)-Tunicaminyluracil, (+)-Tunicamycin-V, and 5'-epi-Tunicamycin-V Journal of the American Chemical Society. 116: 4697-4718. DOI: 10.1021/Ja00090A018  0.718
1993 Kim KH, Kwon BM, Myers AG, Rees DC. Crystal structure of neocarzinostatin, an antitumor protein-chromophore complex. Science (New York, N.Y.). 262: 1042-6. PMID 8235619 DOI: 10.1126/Science.8235619  0.311
1993 Marsh RE, Schaefer WP, Kephart SE, Myers AG. Structure of a syn-aldol addition product of benzaldehyde and a prolinol-derived O-silacyclopentyl ketene N,O-acetal Acta Crystallographica Section C Crystal Structure Communications. 49: 185-188. DOI: 10.1107/S0108270192008825  0.32
1993 Myers AG, Condroski KR. Synthesis of (±)-7,8-epoxy-4-basmen-6-one by a transannular cyclization strategy Journal of the American Chemical Society. 115: 3057-3083. DOI: 10.1021/Ja00070A068  0.32
1993 Myers AG, Dragovich PS. A reaction cascade leading to 1,6-didehydro[10]annulene .fwdarw. 1,5-dehydronaphthalene cyclization initiated by thiol addition Journal of the American Chemical Society. 115: 7021-7022. DOI: 10.1021/Ja00068A089  0.357
1993 Myers AG, Gin DY, Rogers DH. A convergent synthetic route to the tunicamycin antibiotics. Synthesis of (+)-tunicamycin V Journal of the American Chemical Society. 115: 2036-2038. DOI: 10.1021/Ja00058A060  0.797
1992 Marsh RE, Schaefer WP, Kukkola PJ, Myers AG. A chiral N-crotonyloxazolidinone Diels-Alder adduct. Acta Crystallographica. Section C, Crystal Structure Communications. 48: 1622-4. PMID 1445678 DOI: 10.1107/S0108270192000738  0.342
1992 Schaefer WP, Subramanian V, Myers AG. Structure of an 11-membered cyclic silyl enol ether from condensation of methacrolein and a pseudoephedrine-derived O-silyl ketene N,O-acetal Acta Crystallographica Section C Crystal Structure Communications. 48: 2090-2092. DOI: 10.1107/S0108270192006851  0.321
1992 Myers AG, Finney NS. Synthesis of 1,6-didehydro[10]annulene. Observation of its exceptionally facile rearrangement to form the biradical 1,5-dehydronaphthalene Journal of the American Chemical Society. 114: 10986-10987. DOI: 10.1021/Ja00053A059  0.716
1992 Myers AG, Dragovich PS, Kuo EY. Studies on the thermal generation and reactivity of a class of (.sigma.,.pi.)-1,4-biradicals Journal of the American Chemical Society. 114: 9369-9386. DOI: 10.1021/Ja00050A017  0.38
1992 Myers AG, Kephart SE, Chen H. Silicon-directed aldol reactions. Rate acceleration by small rings Journal of the American Chemical Society. 114: 7922-7923. DOI: 10.1021/Ja00046A054  0.311
1992 Myers AG, Dragovich PS. Design and synthesis of a system for enediyne formation by anthraquinone reductive activation Journal of the American Chemical Society. 114: 5859-5860. DOI: 10.1021/Ja00040A057  0.419
1992 Myers AG, Harrington PM, Kwon BM. Evidence for aminoglycoside participation in thiol activation of neocarzinostatin chromophore. Synthesis and reactivity of the epoxy dienediyne core Journal of the American Chemical Society. 114: 1086-1087. DOI: 10.1021/Ja00029A046  0.349
1991 Myers AG, Gin DY, Widdowson KL. Silicon-mediated reductive coupling of aldehydes and allylic alcohols. A stereoselective synthesis of tunicaminyluracil Journal of the American Chemical Society. 113: 9661-9663. DOI: 10.1021/Ja00025A036  0.76
1991 Myers AG, Harrington PM, Kuo EY. Enantioselective synthesis of the epoxy diyne core of neocarzinostatin chromophore Journal of the American Chemical Society. 113: 694-695. DOI: 10.1021/Ja00002A059  0.434
1990 Myers AG, Widdowson KL. A silicon-directed aldol condensation. Synthesis of enantiomerically pure anti aldols Journal of the American Chemical Society. 112: 9672-9674. DOI: 10.1021/Ja00182A056  0.381
1990 Myers AG, Finney NS. Direct observation and retro-ene reaction of a propargylic diazene. Stereochemical assignment of monoalkyl diazenes Journal of the American Chemical Society. 112: 9641-9643. DOI: 10.1021/Ja00182A035  0.676
1990 Myers AG, Kukkola PJ. Stereoselective synthesis of olefins from silylated sulfonylhydrazones Journal of the American Chemical Society. 112: 8208-8210. DOI: 10.1021/Ja00178A078  0.406
1990 MYERS AG, ALAUDDIN MM, FUHRY MM, DRAGOVICH PS, FINNEY NS, HARRINGTON PM. ChemInform Abstract: Versatile Precursors for the Synthesis of Enynes and Enediynes. Cheminform. 21. DOI: 10.1002/chin.199030220  0.702
1990 MYERS AG, FINNEY NS, KUO EY. ChemInform Abstract: Allene Synthesis from 2-Alkyn-1-ols. Cheminform. 21. DOI: 10.1002/chin.199021066  0.705
1990 MYERS AG, KUO EY, FINNEY NS. ChemInform Abstract: Thermal Generation of α,3-Dehydrotoluene from (Z)-1,2,4-Heptatrien-6-yne. Cheminform. 21. DOI: 10.1002/chin.199003098  0.594
1989 Myers AG, Kuo EY, Finney NS. Thermal generation of .alpha.,3-dehydrotoluene from (Z)-1,2,4-heptatrien-6-yne Journal of the American Chemical Society. 111: 8057-8059. DOI: 10.1021/Ja00202A079  0.601
1989 Myers AG, Alauddin MM, Fuhry MAM, Dragovich PS, Finney NS, Harrington PM. Versatile precursors for the synthesis of enynes and enediynes Tetrahedron Letters. 30: 6997-7000. DOI: 10.1016/S0040-4039(01)93407-0  0.689
1989 Myers AG, Finney NS, Kuo EY. Allene synthesis from 2-alkyn-1-ols Tetrahedron Letters. 30: 5747-5750. DOI: 10.1016/S0040-4039(00)76187-9  0.707
1988 Myers AG, Fundy MAM, Lindstrom PA. Mild conditions for the removal of acid-labile protective groups Tetrahedron Letters. 29: 5609-5612. DOI: 10.1016/S0040-4039(00)80825-4  0.327
1987 Corey EJ, Reid JG, Myers AG, Hahl RW. Simple synthetic route to the limonoid system Journal of the American Chemical Society. 109: 918-919. DOI: 10.1021/Ja00237A058  0.58
1987 Myers AG. Proposed structure of the neocarzinostatin chromophore-methyl thioglycolate adduct; A mechanism for the nucleophilic activation of neocarzinostatin Tetrahedron Letters. 28: 4493-4496. DOI: 10.1016/S0040-4039(00)96545-6  0.339
1987 Yamane H, Nohara K, Takahashi N, Corey E, Myers AG, Schraudolft H, Takeno K. Biological activity of antheridic acid, an antheridiogen of anemia phyllitidis Phytochemistry. 26: 1855-1857. DOI: 10.1016/S0031-9422(00)81715-X  0.508
1987 COREY EJ, REID JG, MYERS AG, HAHL RW. ChemInform Abstract: Simple Synthetic Route to the Limonoid System. Cheminform. 18. DOI: 10.1002/chin.198724285  0.541
1986 Corey E, Myers AG, Takahashi N, Yamane H, Schraudolf H. Constitution of antheridium-inducing factor of anemia phyllitidis Tetrahedron Letters. 27: 5083-5084. DOI: 10.1016/S0040-4039(00)85138-2  0.512
1986 COREY EJ, MYERS AG. ChemInform Abstract: Total Synthesis of (±)-Antheridium-Inducing Factor (A M) of the Fern Anemia phyllitidis. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198601325  0.447
1985 Spadari S, Focher F, Kuenzle C, Corey EJ, Myers AG, Hardt N, Rebuzzini A, Ciarrocchi G, Pedrali-Noy G. In vivo distribution and activity of aphidicolin on dividing and quiescent cells. Antiviral Research. 5: 93-101. PMID 3925878 DOI: 10.1016/0166-3542(85)90035-X  0.482
1985 Corey EJ, Myers AG. Total synthesis of (.+-.)-antheridium-inducing factor (AAn) of the Fern Anemia phyllitidis. Clarification of stereochemistry Journal of the American Chemical Society. 107: 5574-5576. DOI: 10.1021/Ja00305A067  0.559
1984 Corey E, Myers AG. Efficient synthesis and intramolecular cyclopropanation of unsaturated diazoacetic esters Tetrahedron Letters. 25: 3559-3562. DOI: 10.1016/S0040-4039(01)91075-5  0.625
1984 COREY EJ, MYERS AG. ChemInform Abstract: EFFICIENT SYNTHESIS AND INTRAMOLECULAR CYCLOPROPANATION OF UNSATURATED DIAZOACETIC ESTERS Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198451120  0.373
1981 Roush WR, Myers AG. Antibiotic X-14547A: total synthesis of the right-hand half The Journal of Organic Chemistry. 46: 1509-1511. DOI: 10.1021/Jo00320A060  0.459
1981 ROUSH WR, MYERS AG. ChemInform Abstract: ANTIBIOTIC X-14547A: TOTAL SYNTHESIS OF THE RIGHT-HAND HALF Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198133345  0.397
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