Shyam Krishnan, Ph.D.
Affiliations: | Harvard University, Cambridge, MA, United States |
Area:
Chemical biologyGoogle:
"Shyam Krishnan"Mean distance: 7.32 | S | N | B | C | P |
Parents
Sign in to add mentor| Stuart L. Schreiber | grad student | 2004 | Harvard | |
| (Diversity-oriented synthesis of biaryl -containing medium rings for chemical genetic studies.) | ||||
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Publications
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| Nanda A, Krishnan S, Kaur H, et al. (2015) Correction of microstomia in an edentulous patient. The Journal of Prosthetic Dentistry |
| London N, Miller RM, Krishnan S, et al. (2015) Erratum: Covalent docking of large libraries for the discovery of chemical probes. Nature Chemical Biology. 11: 235 |
| Han SJ, Vogt F, May JA, et al. (2015) Evolution of a unified, stereodivergent approach to the synthesis of communesin F and perophoramidine. The Journal of Organic Chemistry. 80: 528-47 |
| London N, Miller RM, Krishnan S, et al. (2014) Covalent docking of large libraries for the discovery of chemical probes. Nature Chemical Biology. 10: 1066-72 |
| Krishnan S, Miller RM, Tian B, et al. (2014) Design of reversible, cysteine-targeted Michael acceptors guided by kinetic and computational analysis. Journal of the American Chemical Society. 136: 12624-30 |
| Krishnan S, Miller RM, Tian B, et al. (2014) Correction to “Design of Reversible, Cysteine-Targeted Michael Acceptors Guided by Kinetic and Computational Analysis” Journal of the American Chemical Society. 136: 17690-17690 |
| Miller RM, Paavilainen VO, Krishnan S, et al. (2013) Electrophilic fragment-based design of reversible covalent kinase inhibitors. Journal of the American Chemical Society. 135: 5298-301 |
| Serafimova IM, Pufall MA, Krishnan S, et al. (2012) Reversible targeting of noncatalytic cysteines with chemically tuned electrophiles. Nature Chemical Biology. 8: 471-6 |
| Krishnan S, Stoltz BM. (2007) Preparation of 3,3-disubstituted oxindoles by addition of malonates to 3-halo-3-oxindoles Tetrahedron Letters. 48: 7571-7573 |
| Krishnan S, Schreiber SL. (2004) Syntheses of stereochemically diverse nine-membered ring-containing biaryls. Organic Letters. 6: 4021-4 |