biblio

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Filters: First Letter Of Title is S and Author is Hazra, Braja G.  [Clear All Filters]
2005
B. G. Hazra, Kumar, T. P., and Pore, V. S., “Stereoselective synthesis of (2R, 3S, 22R, 23E)-6, 6-ethylenedioxy-22-hydroxy-2, 3-isopropylidenedioxy-24-methyl-5 alpha-cholest-23-ene: An intermediate for the synthesis of castasterone, dolichosterone and brassinolide”, Indian Journal of Chemistry Section B-Organic Chemistry including Medicinal Chemistry, vol. 44, no. 3, pp. 611-614, 2005.
2006
B. B. Shingate, Hazra, B. G., Pore, V. S., Gonnade, R. G., and Bhadbhade, M. M., “Stereoselective syntheses of unnatural steroidal C(20R) aldehydes by ionic hydrogenation of C-20 tertiary alcohols”, Tetrahedron Letters, vol. 47, no. 52, pp. 9343-9347, 2006.
2007
N. S. Vatmurge, Hazra, B. G., and Pore, V. S., “Syntheses of 1,2-amino alcohols and their applications for oxazaborolidine catalyzed enantioselective reduction of aromatic ketones”, Australian Journal of Chemistry, vol. 60, no. 3, pp. 196-204, 2007.
2008
N. S. Vatmurge, Hazra, B. G., Pore, V. S., Shirazi, F., Chavan, P. S., and Deshpande, M. V., “Synthesis and antimicrobial activity of beta-lactam-bile acid conjugates linked via triazole”, Bioorganic & Medicinal Chemistry Letters, vol. 18, no. 6, pp. 2043-2047, 2008.
N. S. Vatmurge, Hazra, B. G., Pore, V. S., Shirazi, F., Deshpande, M. V., Kadreppa, S., Chattopadhyay, S., and Gonnade, R. G., “Synthesis and biological evaluation of bile acid dimers linked with 1,2,3-triazole and bis-beta-lactam”, Organic & Biomolecular Chemistry, vol. 6, no. 20, pp. 3823-3830, 2008.
S. N. Bavikar, Salunke, D. B., Hazra, B. G., Pore, V. S., Dodd, R. H., Thierry, J., Shirazi, F., Deshpande, M. V., Kadreppa, S., and Chattopadhyay, S., “Synthesis of chimeric tetrapeptide-linked cholic acid derivatives: impending synergistic agents”, Bioorganic & Medicinal Chemistry Letters, vol. 18, no. 20, pp. 5512-5517, 2008.
2013
B. B. Shingate, Hazra, B. G., Salunke, D. B., Pore, V. S., Shirazi, F., and Deshpande, M. V., “Synthesis and antimicrobial activity of novel oxysterols from lanosterol”, Tetrahedron, vol. 69, no. 52, pp. 11155-11163, 2013.