A Highly Stereospecific Procedure for the Transformation of Allylic Alcohols into 1,3-Dienes
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/52/6/52_6_1752/_pdf
Reference19 articles.
1. General method for the synthesis of 1,3-dienes. Simple syntheses of .beta.- and trans-.alpha.-farnescene from farnesol
2. Organoaluminum reagents of type R1R2NAlEt2 which allow regiospecific isomerization of epoxides to allylic alcohols
3. High stereo- and regioselectivities in the transition metal catalyzed epoxidations of olefinic alcohols by tert-butyl hydroperoxide
4. Stereoselective epoxidations of acyclic allylic alcohols by transition metal-hydroperoxide reagents. Synthesis of dl-C18 Cecropia juvenile hormone from farnesol
5. Chiral hydroxamic acids as ligands in the vanadium catalyzed asymmetric epoxidation of allylic alcohols by tert-butyl hydroperoxide
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