Research Group Publications
 
  • Paymode D. J. And Ramana C. V. , “Ruthenium(II)-Catalyzed C3 Arylation of 2-Aroylbenzofurans with Arylboronic Acids/Aryltrifluoroborates via Carbonyl-Directed C–H Bond Activation”, J. Org. Chem., 80, 11551 - 11558 (2015), DOI:10.1021/acs.joc.5b01932.
  • Vadhadiya P. M.; Raut J. K. And Ramana C. V, “Studies toward the total synthesis of Cytospolide E”, Tetrahedron., 71, 9088 - 9094 (2015), DOI:10.1016/j.tet.2015.10.018.
  • Das S. And Ramana C. V., “A formal total synthesis of (-)-kumausallene”, Tetrahedron., 71, 8577 - 8584 (2015), DOI:10.1016/j.tet.2015.09.027.
  • Mullapudi V. And C. V. Ramana, “Total synthesis of (+)-petromyroxol”, Tetrahedron Lett., 56, 3933 - 3935 (2015), DOI:10.1016/j.tetlet.2015.04.129.
  • Phatake R. S. And Ramana C. V., “Oxone–acetone mediated Wacker-type oxidation of benzo-fused olefins”, Tetrahedron Lett., 56, 3868 - 3871 (2015), DOI:10.1016/j.tetlet.2015.04.102.
  • Kumar C. V. S.; Ramana C. V. , “Ru-Catalyzed Redox-Neutral Cleavage of the N?O Bond in Isoxazolidines: Isatogens to Pseudoindoxyls via a One-Pot [3 + 2]- Cycloaddition/N?O Cleavage”, Org. Lett., 17, 2870 - 2873 (2015), DOI:10.1021/acs.orglett.5b00837.
  • Phatake R. S.; Ramana C. V. , “Oxone–acetone mediated syn-dioxygenation of benzo-fused olefins”, Tetrahedron Lett., 56, 2183 - 2186 (2015), DOI:10.1016/j.tetlet.2015.03.022.
  • Vadhadiya P. M.; Ramana C. V. , “Total Synthesis of Sinenside A”, Org. Lett., 17, 1724 - 1727 (2015), DOI:10.1021/acs.orglett.5b00505.
  • Chandrababu Naidu Kona; Mahesh H. Shinde and Chepuri V. Ramana , “Gold(I)-catalyzed hydroindolylation of allenyl ethers”, Org. Biomol. Chem., 13, 5358 - 5362 (2015), DOI:10.1039/C5OB00635J.
  • Senthilkumar B.; Gonnade R. G.; C. V. Ramana, “Pd-catalyzed benzylic C–H oxidation of cyclotriveratrylene – product diversity”, Org. Biomol. Chem., 13, 2323 - 2329 (2015), DOI:10.1039/C4OB02469A.
  • Swami A.; Ramana C. V., “Target cum Flexibility: Synthesis of Indolo[1,2-b]isoquinoline Derivatives via Cobalt-Catalyzed [2+2+2] Cyclotrimerization”, Synlett., 26, 604 - 608 (2015), DOI:10.1055/s-0034-1379950.