R
R. Sateesh Chandra Kumar
Researcher at Indian Institute of Chemical Technology
Publications - 14
Citations - 193
R. Sateesh Chandra Kumar is an academic researcher from Indian Institute of Chemical Technology. The author has contributed to research in topics: Total synthesis & Catalysis. The author has an hindex of 9, co-authored 14 publications receiving 185 citations.
Papers
More filters
Journal ArticleDOI
Stereoselective syntheses of 11-α-methoxycurvularin and 11-β-methoxycurvularin
TL;DR: In this paper, a stereoselective synthesis of potent cytotoxic macrolides, 11-α-methoxycurvularin and 11-β-methylcarno-cinnabar, was presented.
Journal ArticleDOI
A simple and efficient enantioselective route to 2,6-disubstituted piperidines: synthesis of (2R,6S)-isosolenopsin A and (2S,6R)-isosolenopsin
R. Sateesh Chandra Kumar,Eppakayala Sreedhar,G. Venkateswar Reddy,K. Suresh Babu,J. Madhusudana Rao +4 more
TL;DR: The enantioselective synthesis of 2,6-cis-disubstituted piperidine alkaloids, (2R,6S)- isosolenopsin A 2 and (2S,6R)-isosolenopin 5 from fire ant venom is described.
Journal ArticleDOI
Synthesis and antiglycation potentials of bergenin derivatives
T. Vijaya Kumar,Ashok Kumar Tiwari,A. Robinson,K. Suresh Babu,R. Sateesh Chandra Kumar,D. Anand Kumar,Amtul Zehra,J. Madhusudna Rao +7 more
TL;DR: Bergenin, major bioactive compound isolated from methanolic extract of Mallotus philippinensis, displayed moderate AGE inhibition activity and a series of derivatives of bergenin (3a-k) containing variety of aromatic acids were synthesized under mild conditions by modification of sugar part.
Journal ArticleDOI
Stereoselective synthesis of dendrobate alkaloid (+)-241D and its C-4 epimer
R. Sateesh Chandra Kumar,G. Venkateswar Reddy,G. Shankaraiah,K. Suresh Babu,J. Madhusudana Rao +4 more
TL;DR: In this article, an efficient stereoselective synthesis of dendrobate alkaloid (+)-241D and its C-4 epimer was achieved from the inexpensive, commercially available starting material decanal (10) in an overall yield of 21.9% and 21.1%, respectively.
Journal ArticleDOI
Stereoselective synthesis (+)-cephalosporolide D
G. Venkateswar Reddy,R. Sateesh Chandra Kumar,Eppakayala Sreedhar,K. Suresh Babu,J. Madhusudana Rao +4 more
TL;DR: A simple and efficient stereoselective synthesis of macrolactone, (+)-cephalosporolide D has been accomplished in 13 steps from inexpensive and commercially available starting materials in an overall yield of 17%, respectively.