Scaffold Diversity from N-Acyliminium Ions.

Chem Rev
Authors
Abstract

N-Acyliminium ions are powerful reactive species for the formation of carbon-carbon and carbon-heteroatom bonds. Strategies relying on intramolecular reactions of N-acyliminium intermediates, also referred to as N-acyliminium ion cyclization reactions, have been employed for the construction of structurally diverse scaffolds, ranging from simple bicyclic skeletons to complex polycyclic systems and natural-product-like compounds. This review aims to provide an overview of cyclization reactions of N-acyliminium ions derived from various precursors for the assembly of structurally diverse scaffolds, covering the literature over the past 12 years (from 2004 to 2015).

Year of Publication
2017
Journal
Chem Rev
Volume
117
Issue
12
Pages
7811-7856
Date Published
2017 Jun 28
ISSN
1520-6890
DOI
10.1021/acs.chemrev.6b00806
PubMed ID
28493667
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