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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

115 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
2018 Mortison JD, Schenone M, Myers JA, Zhang Z, Chen L, Ciarlo C, Comer E, Natchiar SK, Carr SA, Klaholz BP, Myers AG. Tetracyclines Modify Translation by Targeting Key Human rRNA Substructures. Cell Chemical Biology. PMID 30318461 DOI: 10.1016/j.chembiol.2018.09.010  0.72
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  0.72
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  0.76
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  1
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  1
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  1
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  1
2015 Mukherjee H, Chan KP, Andresen V, Hanley ML, Gjertsen BT, Myers AG. Interactions of the natural product (+)-avrainvillamide with nucleophosmin and exportin-1 Mediate the cellular localization of nucleophosmin and its AML-associated mutants. Acs Chemical Biology. 10: 855-63. PMID 25531824 DOI: 10.1021/cb500872g  1
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  0.88
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  1
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  1
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  1
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  1
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  1
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  1
2013 Mellem KT, Myers AG. A simple, scalable synthetic route to (+)- and (-)-pseudoephenamine. Organic Letters. 15: 5594-7. PMID 24138164 DOI: 10.1021/ol402815d  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2010 Flyer AN, Si C, Myers AG. Synthesis of cortistatins A, J, K and L. Nature Chemistry. 2: 886-92. PMID 20861906 DOI: 10.1038/nchem.794  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2006 Spencer JR, Sendzik M, Oeh J, Sabbatini P, Dalrymple SA, Magill C, Kim HM, Zhang P, Squires N, Moss KG, Sukbuntherng J, Graupe D, Eksterowicz J, Young PR, Myers AG, et al. Evaluation of antitumor properties of novel saframycin analogs in vitro and in vivo. Bioorganic & Medicinal Chemistry Letters. 16: 4884-8. PMID 16870445 DOI: 10.1016/j.bmcl.2006.06.085  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  0.92
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  1
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  1
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  1
2000 Myers AG, Yang BH, Chen H. Transformation of pseudoephedrine amides into highly enantiomerically enriched aldehydes, alcohols, and ketones Organic Syntheses. 77: 29-42.  1
2000 Myers AG, Yang BH. Synthesis and diastereoselective alkylation of pseudoephedrine amides Organic Syntheses. 77: 22-28.  1
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.  1
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  1
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  1
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  1
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  1
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  1
1999 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: 57-75.  1
1999 Myers AG, Zheng B. (tert-butyldimethylsilyl)allene Organic Syntheses. 76: 178-186.  1
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  1
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  1
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  1
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  1
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.  1
1997 Myers AG, Zheng B, Movassaghi M. Preparation of the Reagent o-Nitrobenzenesulfonylhydrazide. The Journal of Organic Chemistry. 62: 7507. PMID 11671877  1
1997 Myers AG, Kort ME, Cohen SB, Tom NJ. Enzymatic activation of DNA cleavage by dynemicin A and synthetic analogs. Biochemistry. 36: 3903-8. PMID 9092820 DOI: 10.1021/bi962976n  1
1997 Myers AG, Zheng B, Movassaghi M. Preparation of the reagent o-nitrobenzenesulfonylhydrazide Journal of Organic Chemistry. 62: 7507. DOI: 10.1021/jo9710137  1
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  1
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  1
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  1
1997 Myers AG, Kort ME, Hammond M. A comparison of DNA cleavage by neocarzinostatin chromophore and its aglycon: Evaluating the role of the carbohydrate residue Journal of the American Chemical Society. 119: 2965-2972. DOI: 10.1021/ja9641719  1
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  1
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  1
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  1
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  1
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.  1
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  1
1996 Myers AG, Parrish CA. DNA cleavage by an alpha, 3-dehydrotoluene precursor conjugated to a minor groove binding element. Bioconjugate Chemistry. 7: 322-31. PMID 8816955 DOI: 10.1021/bc9600170  1
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  1
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  1
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  1
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+  1
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  1
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  1
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  1
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  1
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  1
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  1
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  0.4
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  1
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