Cu-catalysed transamidation of unactivated aliphatic amides-Reference-Cited by-同舟云学术

Cu-catalysed transamidation of unactivated aliphatic amides

Published:2022 Issue:34 Volume:20 Page:6931-6940
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Kumar Vishal¹,Dhawan Sanjeev¹,Bala Renu¹,Mohite Sachin Balaso¹,Singh Parvesh²,Karpoormath Rajshekhar¹^ORCID

Affiliation:

1. Department of Pharmaceutical Chemistry, Discipline of Pharmaceutical Sciences, College of Health Sciences, University of KwaZulu-Natal (Westville), Durban-4000, South Africa

2. School of Chemistry and Physics, University of KwaZulu-Natal (Westville campus), Private Bag X01, Scottsville, Durban, South Africa

Abstract

Direct transamidation is gaining prominence as a ground-breaking technique that generates a wide variety of amides without the requirement of acid–amine coupling or other intermediate steps.

Funder

National Research Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01152B

Reference58 articles.

1. Metal-catalysed approaches to amide bond formation

2. Amide bond formation: beyond the myth of coupling reagents

3. tRNA-dependent amide bond–forming enzymes in peptide natural product biosynthesis