Visible-light-mediated C(sp<sup>3</sup>)–H functionalization of alkyl arylacetates: an easy approach to <i>S</i>-benzyl dithiocarbamate acetates-Reference-Cited by-同舟云学术

Visible-light-mediated C(sp³)–H functionalization of alkyl arylacetates: an easy approach to S-benzyl dithiocarbamate acetates

Published:2023 Issue:5 Volume:47 Page:2412-2416
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Kumar Mahesh¹,Vishwakarma Ramesh Kumar¹,Preeti ¹,Singh Krishna Nand¹^ORCID

Affiliation:

1. Department of Chemistry, Institute of Science, Banaras Hindu University, Varanasi-221005, India

Abstract

An efficient visible light-promoted C(sp3)–H functionalization of alkyl arylacetates has been developed using CS2 and amines by eosin Y/I2 dual catalysis to achieve the formation of S-benzyl dithiocarbamate acetates.

Funder

Banaras Hindu University

Council of Scientific and Industrial Research, India

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/NJ/D2NJ05285G

Reference50 articles.

1. CH Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals

2. Direct Activation of a Remote C(sp 3 )–H Bond Enabled by a Visible‐Light Photosensitized Allene Moiety

3. C–H bond activation enables the rapid construction and late-stage diversification of functional molecules

4. The medicinal chemist's toolbox for late stage functionalization of drug-like molecules

5. Catalytic Methods for CH Bond Functionalization: Application in Organic Synthesis

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