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Dr Srijit Biswas

vidwan id: 122166
Male

Assistant Professor, Department of Chemistry
Calcutta University

Expertise

  • Organic Chemistry

Publications

Total Articles 45
Books 0
Proceedings 0

Publications

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Scopus

Citations 1677
h-index 21

CrossRef

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Citations 954
h-index 15
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Bio

Organic Chemistry

Personal Details

  • Male
  • Assistant Professor , Calcutta University
  • University of Calcutta
Ph.D
Jadavpur University 2011
Assistant Professor Apr 2018 – Present
Calcutta University | Department of Chemistry

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Scholarly Work

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Scholarly Publications

Nucleophilic ipso-Substitution of Aryl Methyl Ethers through Aryl C-OMe Bond Cleavage; Access to Functionalized Bisthiophenes

Open Access
Article

Brønsted Acid Catalyzed Functionalization of Aromatic Alcohols through Nucleophilic Substitution of Hydroxyl Group

Open Access
Article

Nucleophilic substitution of the hydroxyl group in stereogenic alcohols with chirality transfer

Open Access
Article
Authors: Bunrit A.;Dahlstrand C.;Srifa P.;Olsson S.K.;Huang G.;Biswas S.;Himo F.;Samec J.S.M.

Brønsted Acid-Catalyzed Intramolecular Nucleophilic Substitution of the Hydroxyl Group in Stereogenic Alcohols with Chirality Transfer

Open Access
Article
Authors: Bunrit A.;Dahlstrand C.;Olsson S.K.;Srifa P.;Huang G.;Orthaber A.;Sjöberg P.J.R.;Biswas S.;Himo F.;Samec J.S.M.

One-pot synthesis of keto thioethers by palladium/gold-catalyzed click and pinacol reactions

Open Access
Article
Authors: Cadu A.;Watile R.A.;Biswas S.;Orthaber A.;Sjöberg P.J.R.;Samec J.S.M.

Tandem Pd/Au-catalyzed route to α-sulfenylated carbonyl compounds from terminal propargylic alcohols and thiols

Open Access
Article

Atom-efficient gold(I)-chloride-catalyzed synthesis of α-sulfenylated carbonyl compounds from propargylic alcohols and aryl thiols: Substrate scope and experimental and theoretical mechanistic investigation

Open Access
Article
Authors: Biswas S.;Dahlstrand C.;Watile R.A.;Kalek M.;Himo F.;Samec J.S.M.

The efficiency of the metal catalysts in the nucleophilic substitution of alcohols is dependent on the nucleophile and not on the electrophile

Open Access
Article