| Literature DB >> 31490696 |
Peng-Peng Lin1, Xiang-Lei Han1, Guo-Hua Ye2, Ji-Lin Li1, Qingjiang Li1,3, Honggen Wang1.
Abstract
An oxidative [3 + 2] C-H spiroannulation reaction of 2-alkenylphenols with ynamides has been developed toward the synthesis of spiro[4,5]decane derivatives. This dearomative reaction employs earth-abundant cobalt as the metal catalyst and occurs under rather mild reaction conditions (room temperature). The use of ynamides confers unique reactivity and exclusive regioselectivity. The products bearing an all-carbon quaternary stereogenic center were constructed in generally good yields with good functional group tolerance being observed. Experimental mechanistic studies were conducted, and a possible reaction mechanism is proposed.Entities:
Year: 2019 PMID: 31490696 DOI: 10.1021/acs.joc.9b01750
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354