Stereoselective synthesis of substituted tetrahydropyrans via domino olefin cross-metathesis/intramolecular oxa-conjugate cyclization.

Org Lett

Laboratory of Biostructural Chemistry, Graduate School of Life Sciences, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577, Japan.

Published: April 2010

A novel strategy for the stereoselective synthesis of substituted tetrahydropyrans has been developed on the basis of a domino olefin cross-metathesis/intramolecular oxa-conjugate cyclization catalyzed by the Hoveyda-Grubbs second-generation catalyst.

Download full-text PDF

Source
http://dx.doi.org/10.1021/ol100431mDOI Listing

Publication Analysis

Top Keywords

stereoselective synthesis
8
synthesis substituted
8
substituted tetrahydropyrans
8
domino olefin
8
olefin cross-metathesis/intramolecular
8
cross-metathesis/intramolecular oxa-conjugate
8
oxa-conjugate cyclization
8
tetrahydropyrans domino
4
cyclization novel
4
novel strategy
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!