Sandhya Sandra

Ultrasound-based approach to spiro-2,3-dihydroquinazolin-4(1H)-ones: their in vitro evaluation against chorismate mutase

M. Pal, D. Rambabu, S. Kumar, 2013 .

A new route to indoles via in situ desilylation–Sonogashira strategy: identification of novel small molecules as potential anti-tuberculosis agents

J. Iqbal, M. Pal, A. Nakhi, 2011 .

C-N bond formation under Cu-catalysis: synthesis and in vitro evaluation of N-aryl substituted thieno[2,3-d]pyrimidin-4(3H)-ones against chorismate mutase.

M. Pal, D. Rambabu, P. Misra, 2012, Bioorganic & medicinal chemistry.

AlCl3 induced (hetero)arylation of 2,3-dichloroquinoxaline: a one-pot synthesis of mono/disubstituted quinoxalines as potential antitubercular agents.

M. Pal, K. Chatti, C. Reddy, 2012, Bioorganic & medicinal chemistry.

A Pd-mediated new strategy to functionalized 2-aminochromenes: their in vitro evaluation as potential anti tuberculosis agents.

M. Pal, R. Kapavarapu, P. Misra, 2011, Bioorganic & medicinal chemistry letters.

AlCl3 mediated unexpected migration of sulfonyl groups: regioselective synthesis of 7-sulfonyl indoles of potential pharmacological interest.

M. Pal, C. Reddy, D. Rambabu, 2012, Chemical communications.

A Pd-Mediated New Strategy to Functionalized 2-Aminochromenes: Their in vitro Evaluation as Potential Antituberculosis Agents.

M. Pal, R. Kapavarapu, P. Misra, 2012 .

Cu-mediated N-arylation of 1,2,3-triazin-4-ones: synthesis of fused triazinone derivatives as potential inhibitors of chorismate mutase.

M. Pal, D. Rambabu, P. Misra, 2012, Bioorganic & medicinal chemistry letters.