Stereoselective synthesis of (1S, 3R)-1-aminocyclopentane-1,3-dicarboxylic acid via C-H insertion of alkylidenecarbene
- Author
- OHIRA, Susumu1 ; AKIYAMA, Megumi1 ; KAMIHARA, Kumiko1 ; ISODA, Yuichi1 ; KUBOKI, Atsuhito1
[1] Department of Biological Chemistry, Faculty of Science, Okayama University of Science, 1-1 Ridai-cho, Okayama 700-0005, Japan - Source
Bioscience, biotechnology, and biochemistry. 2002, Vol 66, Num 4, pp 887-891 ; ref : 15 ref
- ISSN
- 0916-8451
- Scientific domain
- Biochemistry, molecular biology, biophysics; General biology; Biotechnology
- Publisher
- Japan Society for Bioscience Biotechnology and Agrochemistry, Tokyo
- Publication country
- Japan
- Document type
- Article
- Language
- English
- Keyword (fr)
- Carbène Cyclopentane dérivé Diacide carboxylique Insertion Synthèse asymétrique Synthèse chimique α-Aminoacide Acétique acide ester 3-[triphénylphosphorylidène]acétonyle Cyclopentane-1,3-dicarboxylique(1-amino) Oxazolidine-3,4-dicarboxylique acide(2,2-diméthyl) ester 3-t-butyle 4-méthyle
- Keyword (en)
- Carbene Cyclopentane derivatives Dicarboxylic acid Insertion Asymmetric synthesis Chemical synthesis α-Aminoacid
- Keyword (es)
- Carbeno Ciclopentano derivado Diácido carboxílico Inserción Síntesis asimétrica Síntesis química α-Aminoácido
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05A Alicyclic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 13696572
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1271/bbb.66.887 
https://dx.doi.org/10.1271/bbb.66.887
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