biblio

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Journal Article
M. Muthukrishnan, Garud, D. R., Joshi, R. R., and Joshi, R. A., Concise synthesis of beta-blockers (S)-metoprolol and (S)-betaxolol using hydrolytic kinetic resolution, Tetrahedron, vol. 63, no. 8, pp. 1872-1876, 2007.
A. A. Kulkarni, Nivangune, N. T., Joshi, R. R., and Joshi, R. A., Continuous flow multipoint dosing approach for selectivity engineering in sulfoxidation, Organic Process Research & Development, vol. 17, no. 10, pp. 1293-1299, 2013.
A. A. Kulkarni, Kalyani, V. S., Joshi, R. A., and Joshi, R. R., Continuous flow nitration of benzaldehyde, Organic Process Research & Development, vol. 13, no. 5, pp. 999-1002, 2009.
A. A. Kulkarni, Nivangune, N. T., Kalyani, V. S., Joshi, R. A., and Joshi, R. R., Continuous flow nitration of salicylic acid, Organic Process Research & Development, vol. 12, no. 5, pp. 995-1000, 2008.
R. A. Joshi, Garud, D. R., Muthukrishnan, M., Joshi, R. R., and Gurjar, M. K., Convenient synthesis of the enantiomerically pure beta-blocker (S)-betaxolol using hydrolytic kinetic resolution, Tetrahedron-Asymmetry, vol. 16, no. 23, pp. 3802-3806, 2005.
S. Sarkar, Swami, S., Soni, S. Kumar, Holien, J. K., Khan, A., Korwar, A. M., Likhite, A. P., Joshi, R. A., Joshi, R. R., and Sarkar, D., Detection of a target protein (GroEl2) in Mycobacterium tuberculosis using a derivative of 1,2,4-triazolethiols, Molecular Diversity, vol. 26, no. 5, pp. 2535-2548, 2022.
J. Tibhe, Sharma, Y., Joshi, R. A., Joshi, R. R., and Kulkarni, A. A., Discontinuous two step flow synthesis of m-aminoacetophenone, Green Processing and Synthesis, vol. 3, no. 4, pp. 279-285, 2014.
D. R. Garud, Jadhav, A. R., Lahore, S. V., Kahar, N. M., Joshi, R. R., Joshi, R. A., and Koketsu, M., First iodocyclization reaction of allene-thioureas: an efficient approach to bicyclic beta-lactams, Tetrahedron Letters, vol. 55, no. 43, pp. 5998-6000, 2014.
N. D. Rode, Sonawane, A. D., Garud, D. R., Joshi, R. R., Joshi, R. A., and Likhite, A. P., First regioselective iodocyclization reaction of 3-aryl-5-(prop-2-ynylthio)-1H-1,2,4-triazoles, Tetrahedron Letters, vol. 56, no. 36, pp. 5140-5144, 2015.
M. Muthukrishnan, More, S. V., Garud, D. R., Ramana, C. V., Joshi, R. R., and Joshi, R. A., Pictet-Spengler cyclization in room temperature ionic liquid: a convenient access to tetrahydro beta-carbolines, Journal of Heterocyclic Chemistry, vol. 43, no. 3, pp. 767-772, 2006.
D. R. Garud, Sonawane, A. D., Auti, J. B., Rode, N. D., Ranpise, V. R., Joshi, R. R., and Joshi, R. A., Regioselective and diastereoselective iodocyclization reaction of alkene-thioureas: an efficient approach to bicyclic beta-lactams, New Journal of Chemistry, vol. 39, no. 12, pp. 9422-9428, 2015.
A. Sonawane, Rode, N. D., Nawale, L. U., Joshi, R. R., Joshi, R. A., Likhite, A. P., and Sarkar, D., Synthesis and biological evaluation of 1,2,4-triazole-3-thione and 1,3,4-oxadiazole-2-thione as anti-mycobacterial agents, Chemical Biology & Drug Design, vol. 90, no. 2, pp. 200-209, 2017.
N. D. Rode, Sonawane, A. D., Nawale, L., Khedkar, V. M., Joshi, R. A., Likhite, A. P., Sarkar, D., and Joshi, R. R., Synthesis, biological evaluation, and molecular docking studies of novel 3-aryl-5-(alkyl-thio)-1H-1,2,4-triazoles derivatives targeting Mycobacterium tuberculosis, Chemical Biology & Drug Design, vol. 90, no. 6, pp. 1206-1214, 2017.
S. Ghosh, Barve, A. C., Kumbhar, A. A., Kumbhar, A. S., Puranik, V. G., Datar, P. A., Sonawane, U. B., and Joshi, R. R., Synthesis, characterization, X-ray structure and DNA photocleavage by cis-dichloro bis(diimine) Co(III) complexes, Journal of Inorganic Biochemistry, vol. 100, no. 3, pp. 331-343, 2006.
D. R. Garud, Rode, N. D., Bathe, S. R., Ranpise, V. S., Joshi, R. A., Joshi, R. R., and Koketsu, M., Synthesis of 3-Thia-1-dethiacephems via Regioselective Iodocyclization Reaction, Synthesis-Stuttgart, vol. 47, no. 24, pp. 3956-3962, 2015.
R. R. Joshi, Barchha, A., Khedkar, V. M., Pissurlenkar, R. R. S., Sarkar, S., Sarkar, D., Joshi, R. R., Joshi, R. A., Shah, A. K., and Coutinho, E. C., Targeting dormant tuberculosis bacilli: results for molecules with a novel pyrimidone scaffold, Chemical Biology & Drug Design, vol. 85, no. 2, pp. 201-207, 2015.