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Synthesis 2004(7): 1029-1032
DOI: 10.1055/s-2004-822316
DOI: 10.1055/s-2004-822316
PAPER
© Georg Thieme Verlag Stuttgart · New York
Stereoselective Synthesis of Highly Functionalized Trifluoromethylated Cyclobutenes
Further Information
Received
20 January 2004
Publication Date:
13 April 2004 (online)
Publication History
Publication Date:
13 April 2004 (online)
Abstract
1,1,1-Trifluoro-4-arylbutan-2,4-diones undergo a smooth reaction with dialkyl acetylenedicarboxylates and triphenylphosphine to produce phosphorus ylide intermediates, which undergo stereoselective intramolecular Wittig reaction to produce dialkyl 4-arylcarbonyl-3-trifluoromethyl-cyclobut-2-ene-1,2-dicarboxylates in good yields.
Key words
intramolecular Wittig reaction - trifluoromethylated cyclobutenes - ylide chemistry
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