| Literature DB >> 26120216 |
T Aaron Bedell1, Graham A B Hone1, Justin Du Bois2, Erik J Sorensen1.
Abstract
A new, concise synthesis of the CCR-5 receptor antagonist maraviroc (UK-427,857) from 3-phenyl-1-propanol has been completed in four steps featuring a site-selective C-H functionalization.Entities:
Keywords: Amination; C-H functionalization; CCR-5; HIV/AIDS; Maraviroc
Year: 2015 PMID: 26120216 PMCID: PMC4477708 DOI: 10.1016/j.tetlet.2015.01.074
Source DB: PubMed Journal: Tetrahedron Lett ISSN: 0040-4039 Impact factor: 2.415