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Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides.

ABSTRACT: The carbocupration reactions of heterosubstituted alkynes allow the regio- and stereoselective formation of vinyl organometallic species. N-Alkynylamides (ynamides) are particularly useful substrates for the highly regioselective carbocupration reaction, as they lead to the stereodefined formation of vinylcopper species geminated to the amide moiety. The latter species are involved in numerous synthetically useful transformations leading to valuable building blocks in organic synthesis. Here we describe in full the results of our studies related to the carbometallation reactions of N-alkynylamides.

SUBMITTER: Minko Y

PROVIDER: S-EPMC3628878 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

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Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides.

Minko Yury Y Pasco Morgane M Chechik Helena H Marek Ilan I

Beilstein journal of organic chemistry 20130313

The carbocupration reactions of heterosubstituted alkynes allow the regio- and stereoselective formation of vinyl organometallic species. N-Alkynylamides (ynamides) are particularly useful substrates for the highly regioselective carbocupration reaction, as they lead to the stereodefined formation of vinylcopper species geminated to the amide moiety. The latter species are involved in numerous synthetically useful transformations leading to valuable building blocks in organic synthesis. Here we ...[more]

PMID: 23616793

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