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.
Main Authors: | Baldwin, J, Adlington, R, Robertson, J |
---|---|
Format: | Journal article |
Language: | English |
Published: |
1988
|
Similar Items
-
CARBOCYCLIC RING EXPANSION REACTIONS VIA RADICAL CHAIN PROCESSES
by: Baldwin, J, et al.
Published: (1988) -
CARBOCYCLIC RING EXPANSION REACTIONS VIA RADICAL CHAIN PROCESSES
by: Baldwin, J, et al.
Published: (1989) -
CARBOCYCLIC RING EXPANSION REACTIONS VIA RADICAL CHAIN PROCESSES .2.
by: Baldwin, J, et al.
Published: (1991) -
Ring expansion reaction via homolytic pathways
by: Robertson, J, et al.
Published: (1990) -
RADICAL REACTIONS IN SYNTHESIS - INTRAMOLECULAR SH2' MACROCYCLISATIONS
by: Baldwin, J, et al.
Published: (1990)