Highly diastereoselective Prins-type cyclisation of cyclopropylvinylic aldehydes mediated by TiCl4Electronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b4/b406362g/

23 July 2004

journal article
Published by Royal Society of Chemistry (RSC) in Chemical Communications

Vol. 36 (16) , 1840-1841
https://doi.org/10.1039/b406362g

Abstract

A novel intramolecular Prins type cyclisation of cyclopropylvinylic aldehydes 1 promoted by TiCl₄ under mild reaction conditions to form cis-cyclic products 2 in high yields has been accomplished.

Keywords

PRINS TYPE
TYPE CYCLISATION
CYCLOPROPYLVINYLIC
EXPERIMENTAL
DIASTEREOSELECTIVE
HTTP
WWW.RSC.ORG/SUPPDATA/CC/B4/B406362G/A
TICL4

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