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Reactivity of 1‐Phenoxy‐2,7‐octadiene under Metathesis Conditions
Author(s) -
Damez Céline,
Bouquillon Sandrine,
Hénin Françoise,
Muzart Jacques
Publication year - 2006
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.200600577
Subject(s) - chemistry , metathesis , rhenium , reactivity (psychology) , catalysis , phenols , salt metathesis reaction , organic chemistry , medicinal chemistry , medicine , alternative medicine , pathology , polymerization , polymer
The metathesis of the internal double bond of 1‐phenoxy‐2,7‐octadiene was found to be mediated by Grubbs catalysts. In the presence of rhenium or tungsten‐based catalysts the reaction was found to afford o ‐substituted phenols. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)