Literature DB >> 25894492

Ring-closing enyne metathesis of terminal alkynes with propargylic hindrance.

Benjamin Laroche1, Morgane Detraz1, Alain Blond1, Lionel Dubost1, Patrick Mailliet2, Bastien Nay1.   

Abstract

The ring closing enyne metathesis of substrates with propargylic hindrance was investigated, revealing the successful combination of the Stewart-Grubbs catalysts and microwave heating sometimes up to 170 °C for oxacycles. Medium-sized rings were obtained from terminal alkynes previously reputed as reluctant substrates. This unmatched combination was applied to the synthesis of carbocycles and oxacycles. In addition, this is the first report on the use of the Stewart Grubbs catalyst in ring closing enyne metatheses.

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Year:  2015        PMID: 25894492     DOI: 10.1021/acs.joc.5b00659

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  Diversity-oriented synthesis of 17-spirosteroids.

Authors:  Benjamin Laroche; Thomas Bouvarel; Martin Louis-Sylvestre; Bastien Nay
Journal:  Beilstein J Org Chem       Date:  2020-04-28       Impact factor: 2.883

  1 in total

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