| 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 |
0.676 |
|
| 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 |
0.609 |
|
| 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 |
0.62 |
|
| 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 |
0.748 |
|
| 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 |
0.626 |
|
| 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 |
0.629 |
|
| 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 |
0.633 |
|
| 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 |
0.58 |
|
| 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 |
0.711 |
|
| 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 |
0.58 |
|
| 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 |
0.788 |
|
| 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 |
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| 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 |
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| 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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