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Journal Article
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.
P. S. Deore, Batwal, R. U., and Argade, N. P., “Synthesis of yangjinhualine A”, Synthesis-Stuttgart, vol. 47, no. 4, pp. 485-488, 2015.
P. Mondal and Argade, N. P., “Synthesis of (+)-harmicine”, Synthesis-Stuttgart, vol. 46, no. 19, pp. 2591-2594, 2014.
P. K. Khanna, Subbarao, V. V. V. S., Wagh, M., Jadhav, P., and Patil, K. R., “Synthesis of fine PbE (E = S, Se) powder from direct in situ reduction of sulphur or selenium”, Materials Chemistry and Physics, vol. 93, no. 1, pp. 91-94, 2005.
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.
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.
M. T. 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.
A. S. Kale, Puranik, V. G., and Deshmukh, A. Rakeeb A., “Practical formal synthesis of D-(+)-biotin from 4-formylazetidin-2-one”, Synthesis-Stuttgart, no. 8, pp. 1159-1164, 2007.
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.
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.
I. V. P. Raj and Sudalai, A., “Facile direct conversion of aldehydes to esters and amides using acetone cyanohydrin”, Tetrahedron Letters, vol. 46, no. 48, pp. 8303-8306, 2005.
P. M. Chincholkar, Kale, A. S., Gumaste, V. K., and Deshmukh, A. Rakeeb A., “Efficient formal synthesis of (S)-dapoxetine from enantiopure 3-hydroxy azetidin-2-one”, Tetrahedron, vol. 65, no. 12, pp. 2605-2609, 2009.
S. P. Chavan, Dhawane, A. N., and Kalkote, U. R., “Efficient and practical total synthesis of (+/-)-alpha-cuparenone”, Synthesis-Stuttgart , no. 24, pp. 3827-3830, 2007.
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.
A. Adhikari and Radhakrishnan, S., “Dopant induced effect on electrocatalytic reduction of nitrobenzene using conducting polypyrrole thin film electrodes”, Journal of Applied Polymer Science, vol. 120, no. 2, pp. 719-724, 2011.
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.
A. S. Paraskar and Sudalai, A., “Co-catalyzed reductive cyclization of azido and cyano substituted alpha,beta-unsaturated esters with NaBH4: enantioselective synthesis of (R)-baclofen and (R)-rolipram”, Tetrahedron, vol. 62, no. 20, pp. 4907-4916, 2006.
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.
S. Shylesh, Kapoor, M. P., Juneja, L. R., Samuel, P. R., Srilakshmi, C., and Singh, A. R., “Catalytic meerwein-ponndorf-verley reductions over mesoporous silica supports: rational design of hydrophobic mesoporous silica for enhanced stability of aluminum doped mesoporous catalysts”, Journal of Molecular Catalysis A-Chemical, vol. 301, no. 1-2, pp. 118-126, 2009.