| Year |
Citation |
Score |
| 2018 |
Chan AN, Wever WJ, Massolo E, Allen SE, Li B. Reducing Holomycin Thiosulfonate to its Disulfide with Thiols. Chemical Research in Toxicology. PMID 30523678 DOI: 10.1021/Acs.Chemrestox.8B00243 |
0.388 |
|
| 2018 |
Sardar MYR, Mandhapati AR, Park S, Wever WJ, Cummings RD, Chaikof EL. Convergent synthesis of sialyl LewisX-O-Core-1 threonine. The Journal of Organic Chemistry. PMID 29638128 DOI: 10.1021/Acs.Joc.7B03117 |
0.341 |
|
| 2017 |
Gober JG, Ghodge SV, Bogart JW, Wever WJ, Watkins RR, Brustad EM, Bowers AA. P450-Mediated Non-natural Cyclopropanation of Dehydro-alanine-containing Thiopeptides. Acs Chemical Biology. PMID 28535034 DOI: 10.1021/Acschembio.7B00358 |
0.612 |
|
| 2017 |
Lauinger L, Li J, Shostak A, Cemel IA, Ha N, Zhang Y, Merkl PE, Obermeyer S, Stankovic-Valentin N, Schafmeier T, Wever WJ, Bowers AA, Carter KP, Palmer AE, Tschochner H, et al. Thiolutin is a zinc chelator that inhibits the Rpn11 and other JAMM metalloproteases. Nature Chemical Biology. PMID 28459440 DOI: 10.1038/Nchembio.2370 |
0.605 |
|
| 2017 |
Chan AN, Shiver AL, Wever WJ, Razvi SZ, Traxler MF, Li B. Role for dithiolopyrrolones in disrupting bacterial metal homeostasis. Proceedings of the National Academy of Sciences of the United States of America. PMID 28209778 DOI: 10.1073/Pnas.1612810114 |
0.382 |
|
| 2016 |
Wever WJ, Bogart JW, Bowers AA. Identification of Pyridine Synthase Recognition Sequences Allows Modular Solid-Phase Route to Thiopeptide Variants. Journal of the American Chemical Society. PMID 27575591 DOI: 10.1021/Jacs.6B05389 |
0.644 |
|
| 2015 |
Wever WJ, Bogart JW, Baccile JA, Chan AN, Schroeder FC, Bowers AA. Chemoenzymatic synthesis of thiazolyl peptide natural products featuring an enzyme-catalyzed formal [4 + 2] cycloaddition. Journal of the American Chemical Society. 137: 3494-7. PMID 25742119 DOI: 10.1021/Jacs.5B00940 |
0.69 |
|
| 2015 |
Dunn ZD, Wever WJ, Economou NJ, Bowers AA, Li B. Enzymatic basis of "hybridity" in thiomarinol biosynthesis. Angewandte Chemie (International Ed. in English). 54: 5137-41. PMID 25726835 DOI: 10.1002/Anie.201411667 |
0.658 |
|
| 2015 |
Li B, Wever WJ, Walsh CT, Bowers AA. Correction: Dithiolopyrrolones: biosynthesis, synthesis, and activity of a unique class of disulfide-containing antibiotics. Natural Product Reports. 32: 348-9. PMID 25598489 DOI: 10.1039/C4Np90047B |
0.653 |
|
| 2014 |
Li B, Wever WJ, Walsh CT, Bowers AA. Dithiolopyrrolones: biosynthesis, synthesis, and activity of a unique class of disulfide-containing antibiotics. Natural Product Reports. 31: 905-23. PMID 24835149 DOI: 10.1039/C3Np70106A |
0.663 |
|
| 2013 |
Wever WJ, Cinelli MA, Bowers AA. Visible light mediated activation and O-glycosylation of thioglycosides. Organic Letters. 15: 30-3. PMID 23256636 DOI: 10.1021/Ol302941Q |
0.557 |
|
| 2011 |
Kaur P, Wever W, Pindi S, Milles R, Gu P, Shi M, Li G. The GAP chemistry for chiral N-phosphonyl imine-based Strecker reaction Green Chemistry. 13: 1288-1292. DOI: 10.1039/C1Gc15029D |
0.324 |
|
| 2010 |
Jiang B, Rajale T, Wever W, Tu SJ, Li G. Multicomponent reactions for the synthesis of heterocycles. Chemistry, An Asian Journal. 5: 2318-35. PMID 20922748 DOI: 10.1002/Asia.201000310 |
0.321 |
|
| 2010 |
Kaur P, Pindi S, Wever W, Rajale T, Li G. Asymmetric catalytic N-phosphonyl imine chemistry: the use of primary free amino acids and Et2AlCN for asymmetric catalytic Strecker reaction. The Journal of Organic Chemistry. 75: 5144-50. PMID 20597482 DOI: 10.1021/Jo100865Q |
0.376 |
|
| 2010 |
Ma N, Jiang B, Zhang G, Tu S, Wever W, Li G. New multicomponent domino reactions (MDRs) in water: highly chemo-, regio- and stereoselective synthesis of spiro{[1,3]dioxanopyridine}-4,6-diones and pyrazolo[3,4-b]pyridines Green Chemistry. 12: 1357-1361. DOI: 10.1039/C0Gc00073F |
0.358 |
|
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