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Journal article

Stereospecific anti SE2' fluorination of allenylsilanes: synthesis of enantioenriched propargylic fluorides.

Abstract:
The electrophilic fluorodesilylation of enantioenriched allenylsilanes proceeds with efficient transfer of chirality. The silylation-fluorination of propargylic alcohols occurs with overall retention of stereochemistry, a result consistent with a stereospecific anti S(E)2' mechanism for the fluorination step.
Publication status:
Published

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Publisher copy:
10.1039/b803888k

Authors

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


Journal:
Organic and biomolecular chemistry More from this journal
Volume:
6
Issue:
10
Pages:
1731-1733
Publication date:
2008-05-01
DOI:
EISSN:
1477-0539
ISSN:
1477-0520


Language:
English
Pubs id:
pubs:34225
UUID:
uuid:0c2f744b-68bc-4055-bbae-c333efd95614
Local pid:
pubs:34225
Source identifiers:
34225
Deposit date:
2012-12-19
ARK identifier:

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