biblio

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Journal Article
A. S. Paraskar and Sudalai, A., Cu(OTf)(2) or Et3N-catalyzed three-component condensation of aldehydes, amines and cyanides: a high yielding synthesis of alpha-aminonitriles, Tetrahedron Letters, vol. 47, no. 32, pp. 5759-5762, 2006.
M. A. Kulkarni, Pandit, K. S., Desai, U. V., Lad, U. P., and Wadgaonkar, P. P., Diethylamine: a smart organocatalyst in eco-safe and diastereoselective synthesis of medicinally privileged 2-amino-4H-chromenes at ambient temperature, Comptes Rendus Chimie, vol. 16, no. 8, pp. 689-695, 2013.
A. Awasthi, Mukherjee, A., Singh, M., Rathee, G., Vanka, K., and Chandra, R., Highly efficient chemoselective N-tert butoxycarbonylation of aliphatic/aromatic/heterocyclic amines using diphenylglycoluril as organocatalyst, Tetrahedron, vol. 76, no. 23, p. 131223, 2020.
S. P. Sancheti, Akram, M. O., Roy, R., Bedi, V., Kundu, S., and Patil, N. T., Ortho-oxygenative 1,2-difunctionalization of diarylalkynes under merged gold/organophotoredox relay catalysis, Chemistry-An Asian Journal, 2019.
M. A. Kulkarni, Pandurangi, V. R., Desai, U. V., and Wadgaonkar, P. P., Practical and highly efficient protocol for multicomponent synthesis of beta-phosphonomalononitriles and 2-amino-4H-chromen-4-yl phosphonates using diethylamine as a novel organocatalyst, Comptes Rendus Chimie, vol. 15, no. 9, pp. 745-752, 2012.
K. S. Pandit, Kupwade, R. V., Chavan, P. V., Desai, U. V., Wadgaonkar, P. P., and Kodam, K. M., Problem solving and environmentally benign approach toward diversity oriented synthesis of novel 2-amino-3-phenyl (or Alkyl) sulfonyl-4H-chromenes at ambient temperature, ACS Sustainable Chemistry & Engineering, vol. 4, pp. 3450-3464, 2016.
R. L. Sutar and Joshi, N. N., Role of additives in chiral amine-catalyzed direct aldol reaction, Synthetic Communications, vol. 44, no. 3, pp. 352-360, 2014.
U. V. Desai, Kulkarni, M. A., Pandit, K. S., Kulkarni, A. M., and Wadgaonkar, P. P., Simple, economical, and environmentally benign protocol for the synthesis of 2-amino-3,5-dicarbonitrile-6-sulfanylpyridines at ambient temperature, Green Chemistry Letters and Reviews, vol. 7, no. 3, pp. 228-235, 2014.