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Patil, Krishnaswamy, S., Sarmah, M. P., and Shashidhar, M. S., ?Protecting group directed stereoselective reduction of an epi-inosose: efficient synthesis of epi-inositol?, Tetrahedron Letters, vol. 52, no. 29, pp. 3756-3758, 2011.\par \par R. C.  Jagdhane, Patil, M. T., Krishnaswamy, S., and Shashidhar, M. S., ?Orientation of the beta-hydroxyl group controls the diastereoselectivity during the hydride reduction and grignard reaction of inososes?, Tetrahedron, vol. 69, no. 25, pp. 5144-5151, 2013.\par \par 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.\par \par R. B.  Mane, Jeong, D. - W., Malawadkar, A. V., Roh, H. - S., and Rode, C. V., ?Effect of composition and pretreatment parameters on activity and stability of Cu-Al catalysts for water-gas shift reaction?, ChemCatChem, vol. 6, no. 6, pp. 1698-1706, 2014.\par \par P.  Mondal and Argade, N. P., ?Synthesis of (+)-harmicine?, Synthesis-Stuttgart, vol. 46, no. 19, pp. 2591-2594, 2014.\par \par S. M.  Bhosale, Momin, A. A., Kunjir, S., Rajamohanan, P. R., and Kusurkar, R. S., ?Unexpected observations during the total synthesis of calothrixin B-sodium methoxide as a source of hydride?, Tetrahedron Letters, vol. 55, no. 1, pp. 155-162, 2014.\par \par K.  Hareesh, Joshi, R. P., Shateesh, B., Asokan, K., Kanjilal, D., Late, D. J., Dahiwale, S. S., Bhoraskar, V. N., Haram, S. K., and Dhole, S. D., ?Reduction of graphene oxide by 100 MeV Au ion irradiation and its application as H2O2 sensor?, Journal of Physics D-Applied Physics, vol. 48, no. 36, p. 365105, 2015.\par \par P. S.  Deore, Batwal, R. U., and Argade, N. P., ?Synthesis of yangjinhualine A?, Synthesis-Stuttgart, vol. 47, no. 4, pp. 485-488, 2015.\par \par R. U.  Batwal and Argade, N. P., ?Chemoenzymatic access to (+)-artabotriol and its application in collective synthesis of (+)-grandiamide D, (-)-tulipalin B, (+)-spirathundiol, and (+)-artabotriolcaffeate?, Synthesis-Stuttgart, vol. 48, no. 13, pp. 2130-2136, 2016.\par \par P.  Mondal and Argade, N. P., ?Formal synthesis of bioactive indole alkaloids eburnamonine, eburnaminol, and vindeburnol?, Synthesis-Stuttgart, vol. 49, no. 8, pp. 1849-1856, 2017.\par \par V.  Kumar, Gonnade, R. G., Yildiz, C. B., and Majumdar, M., ?Stabilization of the elusive antimony(I) cation and its coordination complexes with transition metals?, Angewandte Chemie-International Edition, vol. 60, no. 48, pp. 25522-25529, 2021.\par \par P.  Shekhar, Kosugi, K., Singh, H. Dev, Kushwaha, R., Rase, D., Matsuzaki, T., Jain, C., Singh, P., Singh, Y., Vinod, C. Prabhakara, Kondo, M., Masaoka, S., and Vaidhyanathan, R., ?Resorcinol-Azodianiline Covalent Organic Framework Supported FeOOH Quantum Dot-Catalyzed Electrochemical Ammonia Synthesis under Ambient Conditions?, CHEMISTRY OF MATERIALS, vol. 36, pp. 8229-8238, 2024.\par \par A. Vinayak Gavit, Darandale, N. Rajendra, Surange, S. Baburao, and Sawant, D. Nanaji, ?Diboron reagents in modern reduction chemistry: a versatile tool for reduction of various functional groups?, Advanced Synthesis & Catalysis, vol. 367, no. 19, 2025.\par \par }