M. T. Patil

Access to Enantiomeric Organic Compounds with Potential for Synthesis via Racemic Conglomerates: Inositol Derivatives as a Case in Point

R. Gonnade, M. S. Shashidhar, Nivedita T. Patil, 2021 .

An efficient and scalable synthesis of potent TLR2 agonistic PAM2CSK4

Poonam, S. K. Mehta, D. Salunke, 2018, RSC advances.

BBIQ, a pure TLR7 agonist, is an effective influenza vaccine adjuvant

N. Petrovsky, Varun Khanna, D. Salunke, 2020, Human vaccines & immunotherapeutics.

Indole based prostate cancer agents

D. Salunke, M. T. Patil, Sunil Kumar, 2022, Physical Sciences Reviews.

Microwave Assisted Groebke‐Blackburn‐Bienaymé Multicomponent Reaction to Synthesize Imidazo Fused Heterocycles via in‐situ Generated Isocyanides from N ‐formylamines: An Undergraduate Organic Laboratory Experiment

Rahul Singh, Manpreet Kaur, D. Salunke, 2021, Journal of Heterocyclic Chemistry.

The orientation of the β-hydroxyl group controls the diastereoselectivity during the hydride reduction and Grignard reaction of inososes

S. Krishnaswamy, M. S. Shashidhar, R. Jagdhane, 2013 .

Post‐Pictet‐Spengler Cyclization (PPSC): A Strategy to Synthesize Polycyclic β‐Carboline‐Derived Natural Products and Biologically Active N‐Heterocycles

Rahul Singh, D. Salunke, Chung‐Ming Sun, 2020 .

Protecting group directed stereoselective reduction of an epi-inosose: efficient synthesis of epi-inositol

S. Krishnaswamy, M. S. Shashidhar, M. T. Patil, 2011 .

Microemulsions as Nanotemplates: A Soft and Versatile Approach

R. Kanwar, M. T. Patil, J. Rathee, 2018, Microemulsion - a Chemical Nanoreactor [Working Title].

Comparison of racemic epi-inosose and (-)-epi-inosose.

S. Krishnaswamy, M. S. Shashidhar, M. T. Patil, 2011, Acta crystallographica. Section C, Crystal structure communications.