Organic synthesis utilizing Beckmann fragmentation : highly stereoselective C-C bond formation in the reaction of 2,3-isopropylidenedioxycyclohexanone oxime esters with organoaluminium reagents
- Author
- FUJIOKA, H; MIYAZAKI, M; KITAGAWA, H; YAMANAKA, T; YAMAMOTO, H; TAKUMA, K; KITA, Y
Osaka univ., fac. pharmaceutical sci., Suita, Osaka 565, Japan - Source
Journal of the Chemical Society. Chemical communications. 1993, Num 21, pp 1634-1636 ; ref : 4 ref
- CODEN
- JCCCAT
- ISSN
- 0022-4936
- Scientific domain
- Chemistry; Crystallography; Atomic molecular physics
- Publisher
- Royal Society of Chemistry, Cambridge
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acétal Composé bicyclique Cycle 5 chaînons Cétoxime Hétérocycle oxygène Nitrile Racémique Stéréosélectivité Zinc II Chlorure 1,3-Benzodioxol-4-one(2,2-diméthyl-perhydro) [2,6-dichlorobenzoyloxime] 1,3-Benzodioxol-4-one(2,2-diméthyl-perhydro) acétyloxime 1,3-Dioxolane-4-butyrique acide(2,2-diméthyl-5-éthyl) ester méthyle 1,3-Dioxolane-4-butyronitrile(2,2-diméthyl-5-éthyl) 6,8-Dioxobicyclo [3-2-1] octane dérivé Aluminium(trialkyl) Aluminium Composé organique
- Keyword (en)
- Acetal Bicyclic compound Five membered ring Ketoxime Oxygen heterocycle Nitrile Racemate Stereoselectivity Zinc II Chlorides Aluminium Organic compounds
- Keyword (es)
- Acetal Compuesto bicíclico Ciclo 5 eslabones Cetoxima Heterociclo oxígeno Nitrilo Racémico Estereoselectividad Zinc II Cloruro Aluminio Compuesto orgánico
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3961279
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/C39930001634 
https://dx.doi.org/10.1039/C39930001634
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