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Synthesis 2009(2): 335-338
DOI: 10.1055/s-0028-1083275
DOI: 10.1055/s-0028-1083275
PSP
© Georg Thieme Verlag
Stuttgart ˙ New York
Enantioselective Rhodium-Catalyzed Alkylative Desymmetrization of 3,5-Dimethylglutaric Anhydride
Further Information
Received
16 June 2008
Publication Date:
12 December 2008 (online)
Publication History
Publication Date:
12 December 2008 (online)
Abstract
A rhodium-catalyzed enantioselective cross-coupling of sp³ organozinc reagents and 3,5-dimethylglutaric anhydride has been developed to afford the corresponding products, syn-deoxypolypropionates, in excellent yields and enantioselectivities. This reaction has been developed so that both commercially available and in situ prepared organozinc reagents are competent coupling partners.
Key words
organozinc reagents - Grignard reagents - C-C bond formation - syn-deoxypolypropionates
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References
The reaction proceeds in a cleaner fashion if the Grignard is prepared in situ, to avoid by-products arising from oxidation of the organometallic.