Journal article icon

Journal article

Carbocyclic ring expansion reactions via radical chain processes

Abstract:
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.

Actions


Access Document


Publisher copy:
10.1039/C39880001404

Authors


Journal:
Journal of the Chemical Society, Chemical Communications
Issue:
21
Pages:
1404-1406
Publication date:
1988-01-01
DOI:
ISSN:
0022-4936
URN:
uuid:4b1d34c6-2a00-44ac-b4a0-9c21f2b4eb9b
Source identifiers:
326067
Local pid:
pubs:326067
Language:
English

Terms of use


Metrics


Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP