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