| Year |
Citation |
Score |
| 2019 |
Ji C, Sharma I, Pratihar D, Hudson LL, Maura D, Guney T, Rahme LG, Pesci EC, Coleman JP, Tan DS. Designed Small-Molecule Inhibitors of the Anthranilyl-CoA Synthetase PqsA Block Quinolone Biosynthesis in Pseudomonas aeruginosa. Acs Chemical Biology. PMID 31083966 DOI: 10.1021/acschembio.9b00298 |
0.44 |
|
| 2018 |
Kearney SE, Zahoránszky-Kőhalmi G, Brimacombe KR, Henderson MJ, Lynch C, Zhao T, Wan KK, Itkin Z, Dillon C, Shen M, Cheff DM, Lee TD, Bougie D, Cheng K, Coussens NP, ... ... Sharma I, et al. Canvass: A Crowd-Sourced, Natural-Product Screening Library for Exploring Biological Space. Acs Central Science. 4: 1727-1741. PMID 30648156 DOI: 10.1021/acscentsci.8b00747 |
0.44 |
|
| 2016 |
Ji C, Sharma I, Pratihar D, Hudson LL, Maura D, Guney T, Rahme LG, Pesci EC, Coleman JP, Tan DS. Designed Small-Molecule Inhibitors of the Anthranilyl-CoA Synthetase PqsA Block Quinolone Biosynthesis in Pseudomonas aeruginosa. Acs Chemical Biology. PMID 27658001 DOI: 10.1021/acschembio.6b00575 |
0.44 |
|
| 2015 |
Matarlo JS, Evans CE, Sharma I, Lavaud LJ, Ngo SC, Shek R, Rajashankar KR, French JB, Tan DS, Tonge PJ. Mechanism of MenE Inhibition by Acyl-Adenylate Analogues and Discovery of Novel Antibacterial Agents. Biochemistry. PMID 26394156 DOI: 10.1021/acs.biochem.5b00966 |
1 |
|
| 2014 |
Sharma I, Wurst JM, Tan DS. Solvent-dependent divergent functions of Sc(OTf)₃ in stereoselective epoxide-opening spiroketalizations. Organic Letters. 16: 2474-7. PMID 24742081 DOI: 10.1021/ol500853q |
1 |
|
| 2014 |
Váradi A, Palmer TC, Notis PR, Redel-Traub GN, Afonin D, Subrath JJ, Pasternak GW, Hu C, Sharma I, Majumdar S. Three-component coupling approach for the synthesis of diverse heterocycles utilizing reactive nitrilium trapping. Organic Letters. 16: 1668-71. PMID 24580074 DOI: 10.1021/ol500328t |
1 |
|
| 2013 |
Sharma I, Tan DS. Drug discovery: Diversifying complexity. Nature Chemistry. 5: 157-8. PMID 23422555 DOI: 10.1038/nchem.1581 |
1 |
|
| 2012 |
Sharma I, Bohé L, Crich D. Influence of protecting groups on the anomeric equilibrium; Case of the 4,6-O-benzylidene acetal in the mannopyranose series Carbohydrate Research. 357: 126-131. PMID 22739244 DOI: 10.1016/j.carres.2012.05.025 |
1 |
|
| 2012 |
Lu X, Zhou R, Sharma I, Li X, Kumar G, Swaminathan S, Tonge PJ, Tan DS. Stable analogues of OSB-AMP: potent inhibitors of MenE, the o-succinylbenzoate-CoA synthetase from bacterial menaquinone biosynthesis. Chembiochem : a European Journal of Chemical Biology. 13: 129-36. PMID 22109989 DOI: 10.1002/cbic.201100585 |
1 |
|
| 2011 |
Sharma I, Crich D. Direct Fmoc-chemistry-based solid-phase synthesis of peptidyl thioesters Journal of Organic Chemistry. 76: 6518-6524. PMID 21718046 DOI: 10.1021/jo200497j |
1 |
|
| 2011 |
Aubry S, Sasaki K, Sharma I, Crich D. Influence of protecting groups on the reactivity and selectivity of glycosylation: Chemistry of the 4,6-o-benzylidene protected mannopyranosyl donors and related species Topics in Current Chemistry. 301: 141-188. PMID 21240602 DOI: 10.1007/128_2010_102 |
1 |
|
| 2010 |
Crich D, Sharma I. Influence of the O3 protecting group on stereoselectivity in the preparation of C-mannopyranosides with 4,6-O-benzylidene protected donors Journal of Organic Chemistry. 75: 8383-8391. PMID 21070063 DOI: 10.1021/jo101453y |
1 |
|
| 2009 |
Crich D, Sharma I. Triblock peptide and peptide thioester synthesis with reactivity- differentiated sulfonamides and peptidyl thioacids Angewandte Chemie - International Edition. 48: 7591-7594. PMID 19739161 DOI: 10.1002/anie.200903050 |
1 |
|
| 2009 |
Crich D, Sharma I. Epimerization-free block synthesis of peptides from thioacids and amineswith the sanger and mukaiyama reagents Angewandte Chemie - International Edition. 48: 2355-2358. PMID 19229916 |
1 |
|
| 2008 |
Crich D, Sharma I. Is donor-acceptor hydrogen bonding necessary for 4,6-O-benzylidene-directed β-mannopyranosylation? stereoselective synthesis of β-C- mannopyranosides and α-C-glucopyranosides Organic Letters. 10: 4731-4734. PMID 18826233 DOI: 10.1021/ol8017038 |
1 |
|
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