Bioscience, Biotechnology, and Biochemistry
Online ISSN : 1347-6947
Print ISSN : 0916-8451
Organic Chemistry Notes
Stereoselective Synthesis of (1S,3R)-1-Aminocyclopentane-1,3-dicarboxylic Acid via C–H Insertion of Alkylidenecarbene
Susumu OHIRAMegumi AKIYAMAKumiko KAMIHARAYuichi ISODAAtsuhito KUBOKI
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2002 年 66 巻 4 号 p. 887-891

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  (1S,3R)-1-Aminocyclopentane-1,3-dicarboxylic acid (ACPD), a potent agonist of metabotropic glutamate receptors, was synthesized from L-serine. The chiral quaternary center was constructed by C–H insertion of the alkylidenecarbene, this being generated by the reaction between lithiotrimethylsilyldiazomethane and the corresponding ketone.
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© 2002 by Japan Society for Bioscience, Biotechnology, and Agrochemistry
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