| Literature DB >> 24596320 |
Zhiyu Xie1, Lei Liu, Wenfang Chen, Hongbo Zheng, Qingqing Xu, Huiqing Yuan, Hongxiang Lou.
Abstract
Described is a practical and universal CH functionalization of readily removable N-benzyl and N-allyl carbamates, with a wide range of nucleophiles at ambient temperature promoted by Ph3 CClO4 . The metal-free reaction has an excellent functional-group tolerance, and displays a broad scope with respect to both N-carbamates and nucleophile partners (a variety of organoboranes and CH compounds). The synthetic utility in target- as well as diversity-oriented syntheses is demonstrated.Entities:
Keywords: CH functionalization; antitumor agents; nitrogen heterocycles; organoboranes; synthetic methods
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Year: 2014 PMID: 24596320 DOI: 10.1002/anie.201310193
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336