Generic placeholder image

Current Green Chemistry

Editor-in-Chief

ISSN (Print): 2213-3461
ISSN (Online): 2213-347X

Review Article

Allylic Amination via Acid Catalyzed Leaving Group Activation

Author(s): Marija Skvorcova and Aigars Jirgensons

Volume 3, Issue 2, 2016

Page: [145 - 159] Pages: 15

DOI: 10.2174/2213346103666160905101423

Price: $65

Abstract

Background: Allylic amination via acid catalyzed activation of a leaving group is promoted by non-expensive and low toxicity Lewis acid and Bronsted acid catalysts to give valuable allyl amine derivatives. In many cases, non-toxic byproducts such as water or acetic acid are generated. Moreover catalysts that perform the reactions in water as a solvent and the use of recyclable catalysts have been developed.

Methods: Peer-reviewed research literature methods on allylic amination via acid catalyzed activation were compiled using data bases such as Sci-Finder and Scopus.

Results: The mini-review summarizes the most important methods for allylic amination via acid catalyzed activation of a leaving group in the recent decade. These are divide in two main groups - Lewis acid and Bronsted acid catalysed reactions.

Conclusion: Allylic amination via acid catalyzed activation of a leaving group meet criteria of the green chemistry paradigm which has motivated method development for this type of reaction in recent years.

Keywords: Allylic substitution, allylic amination, lewis acids, bronsted acids, green chemistry, allylic alcohols, carbenium ion.

Graphical Abstract

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy