Taming diamines and acyl chlorides by carbon dioxide in selective mono-acylation reactions-Reference-Cited by-同舟云学术

Taming diamines and acyl chlorides by carbon dioxide in selective mono-acylation reactions

Published:2023 Issue:4 Volume:25 Page:1332-1338
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Lauridsen Jerik Mathew Valera¹,Poderyte Margarita¹,Lee Ji-Woong¹²^ORCID

Affiliation:

1. Department of Chemistry, Nano-Science Centre, Universitetsparken 5, Copenhagen Ø, 2100, Denmark

2. Novo Nordisk Foundation CO2 Research Center, Gustav Wieds Vej 10, Aarhus 8000, Denmark

Abstract

Selective monoacylation and unsymmetric diamide formation reactions using acyl chlorides and diamines under ambient CO2 pressure (400 ppm – 1 atm), enabling facile synthesis of bioactive molecules.

Funder

Novo Nordisk

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/GC/D2GC04478A

Reference39 articles.

1. Recent Developments in Amide Synthesis: Direct Amidation of Carboxylic Acids and Transamidation Reactions

2. Biocatalytic Monoacylation of Symmetrical Diamines and Its Application to the Synthesis of Pharmaceutically Relevant Amides

3. Nonclassical Routes for Amide Bond Formation

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

5. Amide Bond Formation Strategies: Latest Advances on a Dateless Transformation

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