Reactivity of (3-chloro-2-methylenecycloalkyl)palladium Chloride Dimers: pd-allyl Cleavage, Synthesis of (±)-13-methyltridecanolide

Authors

William Donaldson, Marquette UniversityFollow
Barbara S. Taylor, Marquette University

Document Type

Article

Language

eng

Publication Date

1985

Publisher

Elsevier

Source Publication

Tetrahedron Letters

Source ISSN

0040-4039

Abstract

The reactions of the title compounds under cleavage conditions affords the corresponding cycloalkenes as the major product. This methodology was used in the synthesis of 13-methyltridecanolide from cyclododecene.

Comments

Tetrahedron Letters, Vol. 26, No. 35 (1985): 4163-4166. DOI.

Recommended Citation

Donaldson, William and Taylor, Barbara S., "Reactivity of (3-chloro-2-methylenecycloalkyl)palladium Chloride Dimers: pd-allyl Cleavage, Synthesis of (±)-13-methyltridecanolide" (1985). Chemistry Faculty Research and Publications. 853.
https://epublications.marquette.edu/chem_fac/853