Journal article

Disubstituted Z-allylic esters by Wittig-Schlosser reaction using methylenetriphenylphosphorane.

Abstract:: β-Lithiooxyphosphonium ylides, generated in situ from aldehydes and methylenetriphenylphosphorane, react with halomethyl esters to form disubstituted allylic esters in good yields and with high Z-selectivity.

Publication status:: Published

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APA Style

Hodgson, D., & Arif, T. (2011). Disubstituted Z-allylic esters by Wittig-Schlosser reaction using methylenetriphenylphosphorane. Chemical Communications, 47(9), 2685–2687.

MLA Style

Hodgson, D., and T. Arif. “Disubstituted Z-Allylic Esters by Wittig-Schlosser Reaction Using Methylenetriphenylphosphorane.” Chemical Communications, vol. 47, no. 9, 2011, pp. 2685–87.

Chicago Style

Hodgson, D, and T Arif. 2011. “Disubstituted Z-Allylic Esters by Wittig-Schlosser Reaction Using Methylenetriphenylphosphorane.” Chemical Communications 47 (9): 2685–87.
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Publisher copy:: 10.1039/c0cc04429f

Authors

+ Hodgson, D More by this author

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

+ Arif, T More by this author

Role:: Author

Journal:: Chemical Communications More from this journal
Volume:: 47
Issue:: 9
Pages:: 2685-2687
Publication date:: 2011-03-01
DOI:: 10.1039/c0cc04429f
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
Pubs id:: pubs:112517
UUID:: uuid:480bd0c0-f9bb-46a0-a7b4-7e9d3e1d401f
Local pid:: pubs:112517
Source identifiers:: 112517
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2011

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

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