Journal article

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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APA Style

Baldwin, J., Adlington, R., & Robertson, J. (1989). CARBOCYCLIC RING EXPANSION REACTIONS VIA RADICAL CHAIN PROCESSES. TETRAHEDRON, 45(4), 909–922.

MLA Style

Baldwin, J., et al. “CARBOCYCLIC RING EXPANSION REACTIONS VIA RADICAL CHAIN PROCESSES.” TETRAHEDRON, vol. 45, no. 4, 1989, pp. 909–22.

Chicago Style

Baldwin, J, R Adlington, and J Robertson. 1989. “CARBOCYCLIC RING EXPANSION REACTIONS VIA RADICAL CHAIN PROCESSES.” TETRAHEDRON 45 (4): 909–22.
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Publisher copy:: 10.1016/0040-4020(89)80003-1

Authors

+ Baldwin, J More by this author

Role:: Author

+ Adlington, R More by this author

Role:: Author

+ Robertson, J More by this author

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:: 10.1016/0040-4020(89)80003-1
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

Terms of use

Copyright date:: 1989

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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