S
Sarabindu Roy
Researcher at Indian Institute of Chemical Technology
Publications - 37
Citations - 952
Sarabindu Roy is an academic researcher from Indian Institute of Chemical Technology. The author has contributed to research in topics: Catalysis & Aryl. The author has an hindex of 16, co-authored 37 publications receiving 903 citations.
Papers
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Journal ArticleDOI
Functionalized nanoparticles as catalysts for enantioselective processes.
Sarabindu Roy,Miquel A. Pericàs +1 more
TL;DR: The different strategies followed for the preparation of chirally modified nanoparticles and their application in asymmetric catalysis are reviewed.
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Nanocrystalline magnesium oxide-stabilized palladium(0): an efficient and reusable catalyst for suzuki and stille cross-coupling of Aryl Halides
TL;DR: In this paper, a nanocrystalline MgO-stabilized nanopalladium (NAPMgPd(0)) catalyst using the basic mgO in place of basic ligands exhibits excellent activity in Su- zuki and Stille cross-coupling of haloarenes (chloro, bromo and iodo) to afford the unsymmetrical biaryls.
Journal ArticleDOI
Polyaniline supported palladium catalyzed Suzuki–Miyaura cross-coupling of bromo- and chloroarenes in water
M. Lakshmi Kantam,Moumita Roy,Sarabindu Roy,Bojja Sreedhar,S. Sakunthala Madhavendra,Boyapati M. Choudary,Rajib Lal De +6 more
TL;DR: Polyaniline supported palladium catalysts were prepared from different palladium precursors and all the catalysts are well characterized using ICP-AES, FTIR, TGA-DTA, SEM-EDX and XPS analysis as discussed by the authors.
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Polyaniline supported CuI: An efficient catalyst for C–N bond formation by N-arylation of N(H)-heterocycles and benzyl amines with aryl halides and arylboronic acids, and aza-Michael reactions of amines with activated alkenes
TL;DR: Polyaniline supported CuI catalyst was used in the N -arylation of N (H)-heterocycles and benzylamines with aryl halides and aryboronic acids and in aza-Michael reaction of amines with activated alkenes.
Journal ArticleDOI
Synthesis of highly substituted 2-perfluoroalkyl quinolines by electrophilic iodocyclization of perfluoroalkyl propargyl imines/amines.
Pravin R. Likhar,M. S. Subhas,Sarabindu Roy,Mannepalli Lakshmi Kantam,Balasubramanian Sridhar,Ratanesh Seth,Sukla Biswas +6 more
TL;DR: The scope of this methodology is extended by using the resulting 2-perfluoroalkyl-3-iodo quinolines in Suzuki, annulation, dehalogenation and carboxylation reactions.