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CARBOCYCLIC RING EXPANSION REACTIONS VIA RADICAL CHAIN PROCESSES

Abstract:
A free radical mediated ring expansion of cis- and trans- α-alkylated-β-stannylcyclohexanones to provide efficient routes tocis- andtrans-cyclononenones and cyclodecenones is described. The cis-/trans- relationship in the precursor was found to have significant bearing on the alkene geometry of the ring expanded product. © 1989.
Publication status:
Published

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author
Journal:
TETRAHEDRON More from this journal
Volume:
45
Issue:
4
Pages:
909-922
Publication date:
1989-01-01
DOI:
ISSN:
0040-4020
Language:
English
Pubs id:
pubs:43223
UUID:
uuid:0c433e35-f7b1-4dbe-92e6-d700fadcde61
Local pid:
pubs:43223
Source identifiers:
43223
Deposit date:
2012-12-19

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