Literature DB >> 31490696

Cp*Co(III)-Catalyzed Dearomative [3 + 2] Spiroannulation of 2-Alkenylphenols with Ynamides via C-H Activation.

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


  1 in total

1.  Electrooxidative palladium- and enantioselective rhodium-catalyzed [3 + 2] spiroannulations.

Authors:  Wen Wei; Alexej Scheremetjew; Lutz Ackermann
Journal:  Chem Sci       Date:  2022-02-10       Impact factor: 9.825

  1 in total

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