| Literature DB >> 28493667 |
Peng Wu1,2,3,4,5,6, Thomas E Nielsen1,2,7.
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).Entities:
Year: 2017 PMID: 28493667 DOI: 10.1021/acs.chemrev.6b00806
Source DB: PubMed Journal: Chem Rev ISSN: 0009-2665 Impact factor: 60.622