Journal article

syn stereocontrol in the directed dihydroxylation of acyclic allylic alcohols

Abstract:: The preparation and directed dihydroxylation of a series of acyclic allylic alcohols is reported. The oxidation reaction is capable of demonstrating high levels of diastereoselection for the syn isomer. An explanation of the observed selectivities based on the degree of allylic strain is presented and a transition state model proposed.

Publication status:: Published

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APA Style

Donohoe, T., Newcombe, N., & Waring, M. (1999). syn stereocontrol in the directed dihydroxylation of acyclic allylic alcohols. TETRAHEDRON LETTERS, 40(38), 6881–6885.

MLA Style

Donohoe, T., et al. “Syn Stereocontrol in the Directed Dihydroxylation of Acyclic Allylic Alcohols.” TETRAHEDRON LETTERS, vol. 40, no. 38, Elsevier, 1999, pp. 6881–85.

Chicago Style

Donohoe, T, N Newcombe, and M Waring. 1999. “Syn Stereocontrol in the Directed Dihydroxylation of Acyclic Allylic Alcohols.” TETRAHEDRON LETTERS 40 (38): 6881–85.
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Publisher copy:: 10.1016/S0040-4039(99)01371-4

Authors

+ Donohoe, T More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Organic Chemistry
Role:: Author

+ Newcombe, N More by this author

Role:: Author

+ Waring, M More by this author

Role:: Author

Publisher:: Elsevier
Journal:: TETRAHEDRON LETTERS More from this journal
Volume:: 40
Issue:: 38
Pages:: 6881-6885
Publication date:: 1999-09-17
DOI:: 10.1016/S0040-4039(99)01371-4
ISSN:: 0040-4039

Language:: English
Pubs id:: pubs:37136
UUID:: uuid:9638a30e-46fd-4652-aebe-4abca892541b
Local pid:: pubs:37136
Source identifiers:: 37136
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 1999

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

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