Silicon compounds as stoichiometric coupling reagents for direct amidation
File(s)d1ob01003d.pdf (4.96 MB)
Published version
Author(s)
Davies, Joshua
Braddock, David
Lickiss, paul
Type
Journal Article
Abstract
Despite being one of the most frequently carried out chemical reactions in industry, there is currently no amidation protocol that is regarded as safe, high yielding, environmentally friendly and inexpensive. The direct amidation of a carboxylic acid with an amine is viewed as an inherently good solution for developing such a protocol. Since the 1960s, there has been a gradual development in the use of silicon reagents for direct amidation. This review covers the methods published to April 2021 for silicon reagent mediated direct amidation of a carboxylic acid with an amine. This review also covers the use of polymeric SiO2 to promote direct amidation.
Date Issued
2021-07-22
Date Acceptance
2021-07-18
Citation
Organic and Biomolecular Chemistry, 2021, 19 (31), pp.6746-6760
ISSN
1477-0520
Publisher
Royal Society of Chemistry
Start Page
6746
End Page
6760
Journal / Book Title
Organic and Biomolecular Chemistry
Volume
19
Issue
31
Copyright Statement
© 2021 The Royal Society of Chemistry. Open Access Article. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
License URL
Identifier
https://pubs.rsc.org/en/content/articlelanding/2021/OB/D1OB01003D
Subjects
Science & Technology
Physical Sciences
Chemistry, Organic
Chemistry
AMIDE BOND FORMATION
CHEMISTRY RESEARCH AREAS
CARBOXYLIC-ACIDS
AMINO-ACIDS
CARBOXAMIDES
PERSPECTIVE
EFFICIENT
TETRACHLORIDE
PHENYLSILANE
ACTIVATION
Organic Chemistry
0304 Medicinal and Biomolecular Chemistry
0305 Organic Chemistry
Publication Status
Published
Date Publish Online
2021-07-22