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Merck
CN

Transforming terpene feedstock into polyketide architecture.

Chemical communications (Cambridge, England) (2010-09-14)
Philipp Winter, Carine Vaxelaire, Christoph Heinz, Mathias Christmann
ABSTRACT

The Cu-catalyzed synthesis of skipped 1,4-dienes from allylic acetates and vinyl-Grignard reagents is key to bidirectional modifications of acyclic terpene acetates. As a result, trisubstituted double bond containing subunits can be readily transferred into complex polyketides from inexpensive bulk terpenes.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
1,4-Cyclohexadiene, purum, ≥97.0% (GC)
Sigma-Aldrich
1,4-Cyclohexadiene, 97%