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Synthesis 2006(20): 3409-3418
DOI: 10.1055/s-2006-950208
DOI: 10.1055/s-2006-950208
PAPER
© Georg Thieme Verlag Stuttgart · New YorkEfficient Synthesis of Fluoroalkenes via Diethylzinc-Promoted Wittig Reaction
Further Information
Received
2 June 2006
Publication Date:
21 August 2006 (online)
Publication History
Publication Date:
21 August 2006 (online)

Abstract
The synthesis of α-fluoroacrylates and α-bromo-α-fluoroalkenes was achieved in very good yields using aldehydes and ketones, triphenylphosphine, diethylzinc as promoter, and ethyl dibromofluoroacetate or dibromofluoromethane, respectively. A change in the addition sequence was critical in order to obtain exclusively α-fluoroacrylates in good yields.
Key words
Wittig reaction - fluoroalkene - ketone - aldehyde - diethylzinc
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