Diversification of α-ketoamides via transamidation reactions with alkyl and benzyl amines at room temperature-Reference-Cited by-同舟云学术

Diversification of α-ketoamides via transamidation reactions with alkyl and benzyl amines at room temperature

Published:2021 Issue:33 Volume:19 Page:7134-7140
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Singh Shweta¹,Popuri Sureshbabu¹,Junaid Qazi Mohammad²,Sabiah Shahulhameed²,Kandasamy Jeyakumar¹^ORCID

Affiliation:

1. Department of chemistry, Indian Institute of Technology (BHU), Varanasi, Uttar Pradesh-221005, India

2. Department of Chemistry, Pondicherry University, Pondicherry-605014, India

Abstract

A wide range of N-tosyl α-ketoamides underwent transamidation with various alkyl and benzyl amines in the absence of a catalyst or base at room temperature. On the other hand, transamidation in N-Boc α-ketoamides was achieved in the presence of Cs2CO3.

Funder

Indian Institute of Technology (BHU) Varanasi

Science and Engineering Research Board

Max-Planck-Gesellschaft

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB01021B

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