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
- 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:
Terms of use
- Copyright date:
- 2008
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