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Synthesis 2005(11): 1901-1905
DOI: 10.1055/s-2004-834920
DOI: 10.1055/s-2004-834920
PSP
© Georg Thieme Verlag Stuttgart · New York
Rhodium-Catalyzed Synthesis of Terminal Alkenes
Further Information
Received
5 October 2004
Publication Date:
24 November 2004 (online)
Publication History
Publication Date:
24 November 2004 (online)
Abstract
Terminal alkenes have been efficiently prepared via a rhodium-catalyzed olefination procedure using Wilkinson’s catalyst in the presence of triphenylphosphine, 2-propanol and trimethylsilyldiazomethane. Optimized reaction conditions are described for aldehydes and ketones, as well as alternative work up procedures.
Key words
terminal alkene - methylenation - trimethylsilyldiazomethane - triphenylphosphine - Wilkinson’s catalyst
- 1 For a review on methylenations, see:
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3a
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3b
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11a This is a modified procedure according to:
Shioiri T.Aoyama T.Mori S. Org. Synth. 1990, 68: 1 -
11b
As trimethylsilyldiazomethane is non-explosive and non-mutagenic, the very careful operations used for the preparation of diazomethane are not necessary.
- 12
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References
Some bottles purchased from Aldrich contain as much as 50% of chloromethyltrimethylsilane by 1H NMR.
13See ref. 11 for analytical procedure.