An efficient and regioselective preparation of 4-oxyazetidin-2-ones from 4-trimethylsilylazetitin-2-ones by use of anodic oxidation
- Author
- SUDA, K1 ; HOTODA, K; WATANABE, J.-I; SHIOZAWA, K; TAKANAMI, T
[1] Meiji coll. pharmacy, Setagaya-ku Tokyo 154, Japan - Source
Journal of the Chemical Society. Perkin transactions. I. 1992, Num 11, pp 1283-1284 ; ref : 6 ref
- CODEN
- JCPRB4
- ISSN
- 0300-922X
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- Royal Society of Chemistry, Cambridge
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Cycle 4 chaînons Hétérocycle azote Lactame Méthane Méthoxylation Oxydation Réaction électrochimique Régiosélectivité Azétidin-2-one(4-méthoxy) Azétidin-2-one(t-triméthylsilyl)
- Keyword (en)
- Four membered ring Nitrogen heterocycle Lactam Methane Methoxylation Oxidation Electrochemical reaction Regioselectivity
- Keyword (es)
- Ciclo 4 eslabones Heterociclo nitrógeno Lactamo Metano Metoxilación Oxidación Reacción electroquímica Regioselectividad
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06B Heterocyclic compounds with only one n hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5339598
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
10.1039/p19920001283 
https://dx.doi.org/10.1039/p19920001283
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