P
Pankaj Das
Researcher at Dibrugarh University
Publications - 71
Citations - 1314
Pankaj Das is an academic researcher from Dibrugarh University. The author has contributed to research in topics: Catalysis & Palladium. The author has an hindex of 18, co-authored 68 publications receiving 1086 citations. Previous affiliations of Pankaj Das include Rajiv Gandhi University of Health Sciences & Council of Scientific and Industrial Research.
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Journal ArticleDOI
Schiff base-derived homogeneous and heterogeneous palladium catalysts for the Suzuki–Miyaura reaction
Pankaj Das,Wolfgang Linert +1 more
TL;DR: In this article, a review of Schiff base-derived homogeneous and heterogeneous palladium catalysts for Suzuki-Miyaura cross-coupling reactions is presented, which provides insights into the state-of-the-art in applications of these Schiff base derived Pd catalysts.
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Biogenic synthesis of palladium nanoparticles and their applications as catalyst and antimicrobial agent.
TL;DR: The starch-assisted PdNPs showed excellent aqueous-phase catalytic activities for three important reactions: the Suzuki-Miyaura cross-coupling reactions of aryl halides with aryalboronic acids; selective oxidations of alcohols to corresponding carbonyl compounds; and reduction of toxic Cr(VI) to nontoxic Cr(III).
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A highly efficient Schiff-base derived palladium catalyst for the Suzuki–Miyaura reactions of aryl chlorides
TL;DR: A palladium complex derived from a bidentate Schiff-base ligand showed excellent activity as catalyst for the Suzuki-Miyaura cross-coupling reactions of less reactive aryl chlorides with arylsboronic acids.
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Highly efficient amine‐based catalytic system for room temperature Suzuki–Miyaura reactions of aryl halides with arylboronic acids
TL;DR: An in situ-generated catalytic system based on PdCl2 and primary amine-based ligand exhibited excellent activity (up to 98% isolated yield) in the Suzuki-Miyaura cross-coupling reactions of aryl bromides with arylsboronic acids in water, at room temperature, without any additive.
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Triphenylphosphine chalcogenides as efficient ligands for room temperature palladium(II)-catalyzed Suzuki–Miyaura reaction
TL;DR: A simple catalytic system based on PdCl 2 and triphenylphosphine chalcogenides (PPh 3 X; X = O, S, Se) was found to be highly effective (up to 97% isolated yield) in the room temperature Suzuki-Miyaura reactions.