| Literature DB >> 18247489 |
Fredy Leon1, Daniel G Rivera, Ludger A Wessjohann.
Abstract
Multiple multicomponent macrocyclizations including bifunctional buildings blocks (MiBs) so far have relied almost exclusively on Ugi reactions. The efficient expansion to non-Ugi-MiBs is exemplified by the synthesis of tetra-beta-lactam and bis-alpha-acyloxy carboxamide macrocycles based on multiple Staudinger and Passerini three-component reactions (3CR), respectively. A recent variation of the Passerini-3CR that involves primary alcohols, isocyanides, and carboxylic acids under oxidative conditions is successfully adapted to this procedure.Entities:
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Year: 2008 PMID: 18247489 DOI: 10.1021/jo7022125
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354