Post‐Pictet‐Spengler Cyclization (PPSC): A Strategy to Synthesize Polycyclic β‐Carboline‐Derived Natural Products and Biologically Active N‐Heterocycles R Singh, S Kumar, MT Patil, CM Sun, DB Salunke Advanced Synthesis & Catalysis 362 (19), 4027-4077, 2020 | 27 | 2020 |
BBIQ, a pure TLR7 agonist, is an effective influenza vaccine adjuvant D Kaushik, S Dhingra, MT Patil, S Piplani, V Khanna, Y Honda-Okubo, ... Human Vaccines & Immunotherapeutics, 1-8, 2020 | 22 | 2020 |
microemulsions as nanotemplates: A soft and versatile approach R Kanwar, J Rathee, MT Patil, SK Mehta Microemulsion—Chemical Nanoreactor, 2019 | 19 | 2019 |
An efficient and scalable synthesis of potent TLR2 agonistic PAM 2 CSK 4 A Kaur, MT Patil, SK Mehta, DB Salunke RSC advances 8 (18), 9587-9596, 2018 | 13 | 2018 |
The orientation of the β-hydroxyl group controls the diastereoselectivity during the hydride reduction and Grignard reaction of inososes RC Jagdhane, MT Patil, S Krishnaswamy, MS Shashidhar Tetrahedron 69 (25), 5144-5151, 2013 | 10 | 2013 |
11. Thiazole: A privileged scaffold in drug discovery S Kumar, MT Patil, R Kataria, DB Salunke Chemical Drug Design, Gupta, GK; Kumar, V., Eds, 243-282, 2016 | 9 | 2016 |
Microwave‐assisted Groebke‐Blackburn‐Bienaymé multicomponent reaction to synthesize imidazo fused heterocycles via in‐situ generated isocyanides from N‐formylamines: An … M Kaur, R Singh, MT Patil, K Kumar, SC Sahoo, KN Singh, VD Chaudhari, ... Journal of Heterocyclic Chemistry 59 (2), 319-328, 2022 | 7 | 2022 |
Protecting group directed stereoselective reduction of an epi-inosose: efficient synthesis of epi-inositol MT Patil, S Krishnaswamy, MP Sarmah, MS Shashidhar Tetrahedron letters 52 (29), 3756-3758, 2011 | 7 | 2011 |
Groebke–Blackburn–Bienaymé multicomponent reaction coupled with unconventional Pictet–Spengler cyclization for the synthesis of imidazo[4,5‐b]pyridine fused … R Singh, R Kumar, M Kaur, MT Patil, SC Sahoo, DB Salunke Journal of Heterocyclic Chemistry, 2022 | 6 | 2022 |
Comparison of racemic epi-inosose and (−)-epi-inosose S Krishnaswamy, MT Patil, MS Shashidhar Acta Crystallographica Section C: Crystal Structure Communications 67 (11 …, 2011 | 4 | 2011 |
Access to Enantiomeric Organic Compounds with Potential for Synthesis via Racemic Conglomerates: Inositol Derivatives as a Case in Point NT Patil, MT Patil, N Sarkar, RG Gonnade, MS Shashidhar Crystal Growth & Design, 2021 | 1 | 2021 |
Chemical drug design T Angelo, R Bhattacharyya, R Kataria, S Kumar, G Mathur, SK Mehta, ... Walter de Gruyter GmbH & Co KG, 2016 | 1 | 2016 |
Indole based prostate cancer agents S Kumar, MT Patil, DB Salunke Physical Sciences Reviews, 2022 | | 2022 |
Synthesis of isomeric cyclitols and their derivatives/analogs from myo-inositol and the associated structural studies MT Patil CSIR-National Chemical Laboratory, Pune, 2012 | | 2012 |