Year |
Citation |
Score |
2023 |
Selby TP, Satterfield AD, Puri A, Stevenson TM, Travis DA, Campbell MJ, Taggi AE, Hughes KA, Bereznak J. Bioisosteric Tactics in the Discovery of Tetflupyrolimet: A New Mode-of-Action Herbicide. Journal of Agricultural and Food Chemistry. PMID 37285594 DOI: 10.1021/acs.jafc.3c01634 |
0.754 |
|
2015 |
Taggi AE, Stevenson TM, Bereznak JF, Sharpe PL, Gutteridge S, Forman R, Bisaha JJ, Cordova D, Crompton M, Geist L, Kovacs P, Marshall E, Sheth R, Stavis C, Tseng CP. Tubulin modulating antifungal and antiproliferative pyrazinone derivatives. Bioorganic & Medicinal Chemistry. PMID 26386818 DOI: 10.1016/J.Bmc.2015.08.038 |
0.301 |
|
2010 |
France S, Wack H, Hafez AM, Taggi AE, Witsil DR, Lectka T. ChemInform Abstract: Bifunctional Asymmetric Catalysis: A Tandem Nucleophile/Lewis Acid Promoted Synthesis of β-Lactams. Cheminform. 33: no-no. DOI: 10.1002/chin.200238091 |
0.632 |
|
2010 |
Wack H, Taggi AE, Hafez AM, Drury III WJ, Lectka T. ChemInform Abstract: Catalytic, Asymmetric α-Halogenation. Cheminform. 32: no-no. DOI: 10.1002/chin.200124065 |
0.567 |
|
2008 |
Schroeder FC, Taggi AE, Gronquist M, Malik RU, Grant JB, Eisner T, Meinwald J. NMR-spectroscopic screening of spider venom reveals sulfated nucleosides as major components for the brown recluse and related species. Proceedings of the National Academy of Sciences of the United States of America. 105: 14283-7. PMID 18794518 DOI: 10.1073/Pnas.0806840105 |
0.763 |
|
2007 |
Dogo-Isonagie C, Bekele T, France S, Wolfer J, Weatherwax A, Taggi AE, Paull DH, Dudding T, Lectka T. A mechanistic study on the catalytic, asymmetric α-bromination of acid chlorides European Journal of Organic Chemistry. 1091-1100. DOI: 10.1002/Ejoc.200600819 |
0.765 |
|
2006 |
Dogo-Isonagie C, Bekele T, France S, Wolfer J, Weatherwax A, Taggi AE, Lectka T. Scalable methodology for the catalytic, asymmetric alpha-bromination of acid chlorides. The Journal of Organic Chemistry. 71: 8946-9. PMID 17081026 DOI: 10.1021/Jo061522L |
0.811 |
|
2005 |
Wang HY, Taggi AE, Meinwald J, Wise RA, Woods AS. Study of the interaction of chlorisondamine and chlorisondamine analogues with an epitope of the alpha-2 neuronal acetylcholine nicotinic receptor subunit. Journal of Proteome Research. 4: 532-9. PMID 15822931 DOI: 10.1021/Pr049786G |
0.461 |
|
2004 |
Taggi AE, Meinwald J, Schroeder FC. A new approach to natural products discovery exemplified by the identification of sulfated nucleosides in spider venom. Journal of the American Chemical Society. 126: 10364-9. PMID 15315451 DOI: 10.1021/Ja047416N |
0.396 |
|
2004 |
France S, Weatherwax A, Taggi AE, Lectka T. Advances in the catalytic, asymmetric synthesis of beta-lactams. Accounts of Chemical Research. 37: 592-600. PMID 15311958 DOI: 10.1021/Ar030055G |
0.821 |
|
2004 |
France S, Wack H, Taggi AE, Hafez AM, Wagerle TR, Shah MH, Dusich CL, Lectka T. Catalytic, asymmetric alpha-chlorination of acid halides. Journal of the American Chemical Society. 126: 4245-55. PMID 15053614 DOI: 10.1021/Ja039046T |
0.824 |
|
2004 |
France S, Wack H, Taggi AE, Hafez AM, Wagerle TR, Shah MH, Dusich CL, Lectka T. Catalytic, Asymmetric α-Chlorination of Acid Halides. Cheminform. 35. DOI: 10.1002/chin.200432037 |
0.616 |
|
2003 |
Hafez AM, Dudding T, Wagerle TR, Shah MH, Taggi AE, Lectka T. A multistage, one-pot procedure mediated by a single catalyst: a new approach to the catalytic asymmetric synthesis of beta-amino acids. The Journal of Organic Chemistry. 68: 5819-25. PMID 12868913 DOI: 10.1021/Jo034150E |
0.847 |
|
2003 |
Taggi AE, Hafez AM, Lectka T. Alpha-imino esters: versatile substrates for the catalytic, asymmetric synthesis of alpha- and beta-amino acids and beta-lactams. Accounts of Chemical Research. 36: 10-9. PMID 12534300 DOI: 10.1021/Ar020137P |
0.798 |
|
2003 |
Taggi AE, Hafez AM, Lectka T. α-Imino Esters: Versatile Substrates for the Catalytic, Asymmetric Synthesis of α- and β-Amino Acids and β-Lactams Cheminform. 34. DOI: 10.1002/chin.200316293 |
0.581 |
|
2002 |
Hafez AM, Taggi AE, Lectka T. Sequential column asymmetric catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 4114-9. PMID 12298001 DOI: 10.1002/1521-3765(20020916)8:18<4114::Aid-Chem4114>3.0.Co;2-Q |
0.745 |
|
2002 |
Taggi AE, Hafez AM, Wack H, Young B, Ferraris D, Lectka T. The development of the first catalyzed reaction of ketenes and imines: catalytic, asymmetric synthesis of beta-lactams. Journal of the American Chemical Society. 124: 6626-35. PMID 12047183 DOI: 10.1021/Ja0258226 |
0.812 |
|
2002 |
France S, Wack H, Hafez AM, Taggi AE, Witsil DR, Lectka T. Bifunctional asymmetric catalysis: a tandem nucleophile/Lewis acid promoted synthesis of beta-lactams. Organic Letters. 4: 1603-5. PMID 11975639 DOI: 10.1021/Ol025805L |
0.825 |
|
2002 |
Taggi AE, Wack H, Hafez AM, France S, Lectka T. Generation of ketenes from acid chlorides using NaH/crown ether shuttle-deprotonation for use in asymmetric catalysis. Organic Letters. 4: 627-9. PMID 11843608 DOI: 10.1021/Ol0172525 |
0.829 |
|
2002 |
Dudding T, Hafez AM, Taggi AE, Wagerle TR, Lectka T. A catalyst that plays multiple roles: asymmetric synthesis of beta-substituted aspartic acid derivatives through a four-stage, one-pot procedure. Organic Letters. 4: 387-90. PMID 11820886 DOI: 10.1021/Ol017087T |
0.848 |
|
2002 |
Ferraris D, Young B, Cox C, Dudding T, Drury WJ, Ryzhkov L, Taggi AE, Lectka T. Catalytic, enantioselective alkylation of alpha-imino esters: the synthesis of nonnatural alpha-amino acid derivatives. Journal of the American Chemical Society. 124: 67-77. PMID 11772063 DOI: 10.1021/Ja016838J |
0.833 |
|
2002 |
Taggi AE, Hafez AM, Dudding T, Lectka T. Molecular mechanics calculations as predictors of enantioselectivity for chiral nucleophile catalyzed reactions Tetrahedron. 58: 8351-8356. DOI: 10.1016/S0040-4020(02)00987-0 |
0.762 |
|
2001 |
Hafez AM, Taggi AE, Dudding T, Lectka T. Asymmetric catalysis on sequentially-linked columns. Journal of the American Chemical Society. 123: 10853-9. PMID 11686686 DOI: 10.1021/Ja016556J |
0.84 |
|
2001 |
Wack H, Taggi AE, Hafez AM, Drury WJ, Lectka T. Catalytic, asymmetric alpha-halogenation. Journal of the American Chemical Society. 123: 1531-2. PMID 11456741 DOI: 10.1021/Ja005791J |
0.774 |
|
2001 |
Hafez AM, Taggi AE, Wack H, Esterbrook J, Lectka T. Reactive ketenes through a carbonate/amine shuttle deprotonation strategy: catalytic, enantioselective alpha-bromination of acid chlorides. Organic Letters. 3: 2049-51. PMID 11418046 DOI: 10.1021/Ol0160147 |
0.818 |
|
2000 |
Hafez AM, Taggi AE, Wack H, Drury WJ, Lectka T. Column asymmetric catalysis for beta-lactam synthesis. Organic Letters. 2: 3963-5. PMID 11112618 DOI: 10.1021/Ol006659R |
0.813 |
|
2000 |
Taggi AE, Hafez AM, Wack H, Young B, Drury WJ, Lectka T. Catalytic, asymmetric synthesis of β-lactams [11] Journal of the American Chemical Society. 122: 7831-7832. DOI: 10.1021/Ja001754G |
0.759 |
|
2000 |
Taggi AE, Hafez AM, Wack H, Young B, Drury III WJ, Lectka T. ChemInform Abstract: Catalytic, Asymmetric Synthesis of β-Lactams. Cheminform. 31: no-no. DOI: 10.1002/chin.200047107 |
0.603 |
|
1999 |
Wack H, Drury WJ, Taggi AE, Ferraris D, Lectka T. Nucleophilic metal complexes as acylation catalysts: solvent-dependent "switch" mechanisms leading to the first catalyzed Staudinger reaction. Organic Letters. 1: 1985-8. PMID 10836055 DOI: 10.1021/Ol9903234 |
0.794 |
|
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