| Literature DB >> 26440560 |
Sang Hoon Han1, Miji Choi1, Taejoo Jeong1, Satyasheel Sharma1, Neeraj Kumar Mishra1, Jihye Park1, Joa Sub Oh2,3, Woo Jung Kim3, Jong Suk Lee3, In Su Kim1.
Abstract
The rhodium(III)-catalyzed site-selective C-H alkylation of various N-heterocycles, such as indolines, carbazoles, and pyrroles with readily available allylic alcohols is described. This protocol allows the generation of a heterocyclic scaffold containing a β-aryl carbonyl moiety, which is known to be a crucial structural unit of biologically active compounds.Entities:
Year: 2015 PMID： 26440560 DOI： 10.1021/acs.joc.5b01696
Source DB: PubMed Journal: J Org Chem ISSN： 0022-3263 Impact factor: 4.354