Carbocyclic ring expansion reactions via radical chain processes

Free radical mediated ring expansion of cis- and trans-α-substituted- β-stannylcyclohexanones provides efficient routes to cis- and trans-cyclononenones and cyclodecenones; the cis-/trans-geometry of the precursor controls the alkene geometry of the ring-expanded product.

Bibliographic Details
Main Authors: Baldwin, J, Adlington, R, Robertson, J
Format: Journal article
Language:English
Published: 1988