S
Srivari Chandrasekhar
Researcher at Indian Institute of Chemical Technology
Publications - 461
Citations - 8395
Srivari Chandrasekhar is an academic researcher from Indian Institute of Chemical Technology. The author has contributed to research in topics: Catalysis & Total synthesis. The author has an hindex of 42, co-authored 453 publications receiving 7798 citations. Previous affiliations of Srivari Chandrasekhar include Academy of Scientific and Innovative Research & University of Texas Southwestern Medical Center.
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Journal ArticleDOI
Inter and intramolecular copper(I)-catalyzed 1,3-dipolar cycloaddition of azido-alkynes: synthesis of furanotriazole macrocycles ☆
Srivari Chandrasekhar,Chennamaneni Lohitha Rao,Chidalla Nagesh,Chada Raji Reddy,Balasubramanian Sridhar +4 more
TL;DR: The Cu(I)-catalyzed cycloaddition of azido-alkynes (click reaction) of furanose sugar substrates provides a facile approach for the construction of macrocyclic molecules via an inter and/or intramolecular cycloadDition based on the functionality between alkyne and azide.
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Synthesis and biological activity of amide derivatives of nimbolide.
B. S. Sastry,K. Suresh Babu,T. Hari Babu,Srivari Chandrasekhar,P.V. Srinivas,Anil K. Saxena,J. Madhusudana Rao +6 more
TL;DR: A series of nimbolide derivatives have been synthesized and evaluated for in vitro cytotoxic activity against a panel of human cancer cell lines and 2g, 2h and 2i showed potent activity.
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Proline-threonine dipeptide as an organocatalyst for the direct asymmetric aldol reaction
TL;DR: A new proline-threonine (H-Pro-Thr-OH) dipeptide has been demonstrated as an efficient organocatalyst for a direct asymmetric aldol Reaction in good yields with good enantioselectivities.
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Chiral pyrrolidine–triazole conjugate catalyst for asymmetric Michael and Aldol reactions
TL;DR: In this article, a new pyrrolidine-triazole conjugate organocatalyst was synthesized using a Huisgen 1,3-dipolar cycloaddition reaction.
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Tris(pentafluorophenyl)borane-Catalyzed Three-Component Reaction for the Synthesis of 1,8-Dioxodecahydroacridines under Solvent-Free Conditions
Srivari Chandrasekhar,Yaragorla Srinivasa Rao,Lella Sreelakshmi,Bodugam Mahipal,Chada Raji Reddy +4 more
TL;DR: In this article, a mild and efficient method for the synthesis of 1,8-dioxodecahydroacridines has been developed via a three-component reaction of a 1,3-dione, an aldehyde and an amine, under solvent-free conditions, catalyzed by tris(pentafluorophenyl)borane.