Albert Bowers
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Ribosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclature
PG Arnison, MJ Bibb, G Bierbaum, AA Bowers, TS Bugni, G Bulaj, ...
Natural product reports 30 (1), 108-160, 2013
Total synthesis and biological mode of action of largazole: a potent class I histone deacetylase inhibitor
A Bowers, N West, J Taunton, SL Schreiber, JE Bradner, RM Williams
Journal of the American Chemical Society 130 (33), 11219-11222, 2008
Electrochemical generation of glycosyl triflate pools
T Nokami, A Shibuya, H Tsuyama, S Suga, AA Bowers, D Crich, ...
Journal of the American Chemical Society 129 (35), 10922-10928, 2007
Structural insights into thioether bond formation in the biosynthesis of sactipeptides
TL Grove, PM Himes, S Hwang, H Yumerefendi, JB Bonanno, B Kuhlman, ...
Journal of the American Chemical Society 139 (34), 11734-11744, 2017
On the Use of 3,5-O-Benzylidene and 3,5-O-(Di-tert-butylsilylene)-2-O-benzylarabinothiofuranosides and Their Sulfoxides as Glycosyl Donors for the Synthesis of …
D Crich, CM Pedersen, AA Bowers, DJ Wink
The Journal of organic chemistry 72 (5), 1553-1565, 2007
Thiopeptide antibiotics stimulate biofilm formation in Bacillus subtilis
R Bleich, JD Watrous, PC Dorrestein, AA Bowers, EA Shank
Proceedings of the National Academy of Sciences 112 (10), 3086-3091, 2015
Synthesis and histone deacetylase inhibitory activity of largazole analogs: alteration of the zinc-binding domain and macrocyclic scaffold
AA Bowers, N West, TL Newkirk, AE Troutman-Youngman, SL Schreiber, ...
Organic letters 11 (6), 1301-1304, 2009
Chemoenzymatic synthesis of thiazolyl peptide natural products featuring an enzyme-catalyzed formal [4+ 2] cycloaddition
WJ Wever, JW Bogart, JA Baccile, AN Chan, FC Schroeder, AA Bowers
Journal of the American Chemical Society 137 (10), 3494-3497, 2015
Synthesis and conformation− activity relationships of the peptide isosteres of FK228 and largazole
AA Bowers, TJ Greshock, N West, G Estiu, SL Schreiber, O Wiest, ...
Journal of the American Chemical Society 131 (8), 2900-2905, 2009
Manipulation of thiocillin variants by prepeptide gene replacement: structure, conformation, and activity of heterocycle substitution mutants
AA Bowers, MG Acker, A Koglin, CT Walsh
Journal of the American Chemical Society 132 (21), 7519-7527, 2010
Inhibition of cell differentiation in Bacillus subtilis by Pseudomonas protegens
MJ Powers, E Sanabria-Valentín, AA Bowers, EA Shank
Journal of bacteriology 197 (13), 2129-2138, 2015
Thiolutin is a zinc chelator that inhibits the Rpn11 and other JAMM metalloproteases
L Lauinger, J Li, A Shostak, IA Cemel, N Ha, Y Zhang, PE Merkl, ...
Nature chemical biology 13 (7), 709-714, 2017
Dithiolopyrrolones: biosynthesis, synthesis, and activity of a unique class of disulfide-containing antibiotics
B Li, WJ Wever, CT Walsh, AA Bowers
Natural product reports 31 (7), 905-923, 2014
Visible Light Mediated Activation and O-Glycosylation of Thioglycosides
WJ Wever, MA Cinelli, AA Bowers
Organic letters 15 (1), 30-33, 2013
Thiazolyl peptide antibiotic biosynthesis: a cascade of post-translational modifications on ribosomal nascent proteins
CT Walsh, MG Acker, AA Bowers
Journal of biological chemistry 285 (36), 27525-27531, 2010
Discovery, biological activity, synthesis and potential therapeutic utility of naturally occurring histone deacetylase inhibitors
TL Newkirk, AA Bowers, RM Williams
Natural product reports 26 (10), 1293-1320, 2009
Generation of Thiocillin Variants by Prepeptide Gene Replacement and in Vivo Processing by Bacillus cereus
MG Acker, AA Bowers, CT Walsh
Journal of the American Chemical Society 131 (48), 17563-17565, 2009
Dehydroamino acids: chemical multi-tools for late-stage diversification
JW Bogart, AA Bowers
Organic & biomolecular chemistry 17 (15), 3653-3669, 2019
Genetic Interception and Structural Characterization of Thiopeptide Cyclization Precursors from Bacillus cereus
AA Bowers, CT Walsh, MG Acker
Journal of the American Chemical Society 132 (35), 12182-12184, 2010
4,6-O-[1-Cyano-2-(2-iodophenyl)ethylidene] Acetals. Improved Second-Generation Acetals for the Stereoselective Formation of β-d-Mannopyranosides and Regioselective …
D Crich, AA Bowers
The Journal of organic chemistry 71 (9), 3452-3463, 2006
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