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Merck
CN
  • Directed epoxidation of cyclohexa-1,4-dienes-stereoselective formation of up to six contiguous stereogenic centres.

Directed epoxidation of cyclohexa-1,4-dienes-stereoselective formation of up to six contiguous stereogenic centres.

Organic & biomolecular chemistry (2008-11-14)
Michael Butters, Dirk J Beetstra, Mark C Elliott, Joseph Hill-Cousins, Benson M Kariuki
摘要

Epoxidation/cyclisation of cyclohexa-1,4-dienes containing pendant hydroxyl groups provides stereocontrolled access to highly-functionalised reduced benzol[b]furan derivatives.

材料
Product Number
品牌
产品描述

Sigma-Aldrich
1,4-环己二烯, 97%
Sigma-Aldrich
1,4-环己二烯, purum, ≥97.0% (GC)