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