Reactions of Phosphites with Nitroalkene Derivatives: Syntheses of $\Beta$-Keto Phosphonates and $\alpha$-Cyanoalkylphosphonates

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The addition of phosphite derivatives 1 to nitroalkenes 2 afforded alpha-phosphoryl nitronates which, on treatment MCPBA, were converted beta-keto phosphonates 3. A versatile reaction conditions to generate alpha-phosphoryl nitronates were examined. alpha-Cyanoalkylphosphonates 6 were prepared from the diethyl trimethylsilyl phosphite (DTSP) 1c with nitroalkenes 2 and followed by reduction.
Publisher
Korean Chemical Soc
Issue Date
1997
Language
English
Article Type
Article
Keywords

ENAMINE PHOSPHONATES; ORGANIC-SYNTHESIS; VINYL PHOSPHATES; FACILE SYNTHESIS; CARBOMYCIN-B; REAGENTS; ACID; KETOPHOSPHONATES; OLEFINS; ESTERS

Citation

BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.18, no.9, pp.994 - 998

ISSN
0253-2964
URI
http://hdl.handle.net/10203/71304
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