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Journal article

Phosphine-Catalysed Cyclisation of beta-Hydroxy-alpha,alpha-Difluoroynones

Abstract:: 2-Benzylidene-4,4-difluorodihydrofuran-3(2H)-ones were synthesised in 58-86% yield via phosphine-promoted cyclisation of β-hydroxy-α, α-difluoroynones. The benzylidene group was found to be a suitable masked carbonyl group, thereby allowing for the validation of a novel route to 3,3-difluoro-2-hydroxy-γ-lactols. © Georg Thieme Verlag Stuttgart.

Publication status:: Published

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APA Style

Schuler, M., Monney, A., & Gouverneur, V. (2009). Phosphine-Catalysed Cyclisation of beta-Hydroxy-alpha,alpha-Difluoroynones. SYNLETT, 2009(11), 1733–1736.

MLA Style

Schuler, M., et al. “Phosphine-Catalysed Cyclisation of Beta-Hydroxy-Alpha,Alpha-Difluoroynones.” SYNLETT, vol. 2009, no. 11, 2009, pp. 1733–36.

Chicago Style

Schuler, M, A Monney, and V Gouverneur. 2009. “Phosphine-Catalysed Cyclisation of Beta-Hydroxy-Alpha,Alpha-Difluoroynones.” SYNLETT 2009 (11): 1733–36.
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Publisher copy:: 10.1055/s-0029-1217366

Authors

+ Schuler, M More by this author

Role:

Author

+ Monney, A More by this author

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Author

+ Gouverneur, V More by this author

Institution:

University of Oxford

Division:

MPLS

Department:

Chemistry

Sub department:

Organic Chemistry

Role:

Author

Bibliographic Details

Journal:: SYNLETT
Volume:: 2009
Issue:: 11
Pages:: 1733-1736
Publication date:: 2009-07-01
DOI:: 10.1055/s-0029-1217366
EISSN:: 1437-2096
ISSN:: 0936-5214

Item Description

Language:: English
Keywords:: phosphine

catalysis

fluorine

furanone
Pubs id:: pubs:41267
UUID:: uuid:61eab7ae-154d-4fff-b311-1a1894c32f41
Local pid:: pubs:41267
Source identifiers:: 41267
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2009

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

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