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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651673PMC
http://dx.doi.org/10.1021/acs.orglett.7b00174DOI Listing

Publication Analysis

Top Keywords

c-h vinylation
8
ruthenium0-catalyzed c-c
4
c-c coupling
4
coupling alkynes
4
alkynes 3-hydroxy-2-oxindoles
4
3-hydroxy-2-oxindoles direct
4
direct c-h
4
vinylation alcohols
4
alcohols exposure
4
exposure ruthenium0
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!