D
Dipankar Srimani
Researcher at Indian Institute of Technology Guwahati
Publications - 53
Citations - 2570
Dipankar Srimani is an academic researcher from Indian Institute of Technology Guwahati. The author has contributed to research in topics: Catalysis & Ruthenium. The author has an hindex of 21, co-authored 43 publications receiving 2013 citations. Previous affiliations of Dipankar Srimani include Indian National Association & Weizmann Institute of Science.
Papers
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Size controlled synthesis of Pd nanoparticles in water and their catalytic application in C–C coupling reactions
TL;DR: In this paper, a reduction of Pd(II) with a Fischer carbene complex where polyethylene glycol (PEG) was used as stabilizer is presented.
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A new functionalized mesoporous matrix supported Pd(II)-Schiff base complex: an efficient catalyst for the Suzuki–Miyaura coupling reaction
Koushik Dhara,Krishanu Sarkar,Dipankar Srimani,Subrata Saha,Pabitra Chattopadhyay,Asim Bhaumik +5 more
TL;DR: A new Pd(II) bounded 2D-hexagonally ordered functionalized MCM-41 type material (IV) has been synthesized and was found that this catalyst is highly efficient and recyclable towards Suzuki-Miyaura reaction with high turn over frequencies.
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Phosphine free Mn-complex catalysed dehydrogenative C–C and C–heteroatom bond formation: a sustainable approach to synthesize quinoxaline, pyrazine, benzothiazole and quinoline derivatives
TL;DR: The first sustainable synthesis of quinoxalines, pyrazines and benzothiazoles catalysed by a phosphine free Mn(i) complex via acceptorless dehydrogenative coupling (ADC) is reported.
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Ruthenium Pincer‐Catalyzed Cross‐Dehydrogenative Coupling of Primary Alcohols with Secondary Alcohols under Neutral Conditions
Dipankar Srimani,Ekambaram Balaraman,Ekambaram Balaraman,Boopathy Gnanaprakasam,Yehoshoa Ben-David,David Milstein +5 more
TL;DR: In this paper, a bipyridyl-based PNN ruthenium(II) pincer catalyst was used for cross-dehydrogenative coupling of primary alcohols with secondary alcohols to obtain mixed esters.
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Selective Synthesis of 2-Substituted and 1,2-Disubstituted Benzimidazoles Directly from Aromatic Diamines and Alcohols Catalyzed by Molecularly Defined Nonphosphine Manganese(I) Complex.
TL;DR: This work presents a selective synthesis of 2-substituted and 1,2-disubstituting benzimidazoles by acceptorless dehydrogenative coupling of aromatic diamine with primary alcohols by phosphine-free tridentate NNS ligand-derived manganese(I) complex.