Bhaumik A. Pandya

An aldol-based build/couple/pair strategy for the synthesis of medium- and large-sized rings: discovery of macrocyclic histone deacetylase inhibitors.

Nathan T. Ross, Carol A. Mulrooney, Jeremy R. Duvall, 2010, Journal of the American Chemical Society.

Synthesis of a novel suppressor of beta-cell apoptosis via diversity-oriented synthesis.

Patrick W. Faloon, Bridget K Wagner, Byung-Chul Suh, 2011, ACS medicinal chemistry letters.

Targeting Bacterial Cell Wall Peptidoglycan Synthesis by Inhibition of Glycosyltransferase Activity

W. Meutermans, M. Conrad, M. Mesleh, 2016, Chemical biology & drug design.

Synthesis of stereochemically and skeletally diverse fused ring systems from functionalized C-glycosides.

Jeremy R. Duvall, M. Foley, L. A. Marcaurelle, 2013, The Journal of organic chemistry.

Large-scale synthesis of all stereoisomers of a 2,3-unsaturated C-glycoside scaffold.

L. A. Marcaurelle, Baudouin Gerard, Maurice D. Lee, 2011, The Journal of organic chemistry.

Practical asymmetric synthesis of β-hydroxy γ-amino acids via complimentary aldol reactions.

Carol A. Mulrooney, Jeremy R. Duvall, D. Young, 2011, Tetrahedron.

Old Drugs Yield New Discoveries: Examples from the Prodrug, Chiral Switch, and Site‐Selective Deuteration Strategies

Bhaumik A. Pandya, C. Masse, S. Harbeson, 2012 .

Structure-activity relationship of daptomycin analogues with substitution at (2S, 3R) 3-methyl glutamic acid position.

Xuechen Li, Bhaumik A. Pandya, H. Lam, 2017, Bioorganic & medicinal chemistry letters.

Discovery of indole inhibitors of chemokine receptor 9 (CCR9).

Bhaumik A. Pandya, M. Varoglu, B. Lippa, 2016, Bioorganic & medicinal chemistry letters.