Upon exposure to a ruthenium(0) catalyst, N-benzyl-3-hydroxy-2-oxindoles react with diverse alkynes to form products of C-H vinylation with complete control of regioselectivity and olefin geometry. This method contributes to a growing body of catalytic processes that enable direct conversion of lower alcohols to higher alcohols in the absence of stoichiometric organometallic reagents.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651673 | PMC |
http://dx.doi.org/10.1021/acs.orglett.7b00174 | DOI Listing |
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