Stereoselective synthesis of 2-oxazoline-4-carboxylates through Lewis acid-catalyzed formal [3+2]cycloadditions of 5-alkyxyoxazoles with aldehydes : catalytic effect of methylaluminum β-binaphthoxide on cis-selectivity
- Author
- SUGA, H; XIAOLAN SHI; IBATA, T
Osaka univ., coll. gen. education, inst. chemistry, Toyonaka, Osaka 560, Japan - Source
Journal of organic chemistry. 1993, Vol 58, Num 26, pp 7397-7405 ; ref : 13 ref
- CODEN
- JOCEAH
- ISSN
- 0022-3263
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aluminium Complexe Aminoester Benzaldéhyde Complexe aryloxy Cycle 5 chaînons Cycloaddition Effet milieu Effet stérique Hétérocycle oxygène azote Réaction catalytique Stéréosélectivité Transposition chimique 1,1p-Binaphtyle-2,2p-diol Aluminium(méthyl complexe) Oxazole(2-aryl-5-méthoxy) Oxazole-4-carboxylique acide(2-aryl-4,5-dihydro-5-phényl) ester méthyle
- Keyword (en)
- Aluminium Complexes Aminoester Benzaldehyde Aryloxy complex Five membered ring Cycloaddition Medium effect Steric effect Oxygen nitrogen heterocycle Catalytic reaction Stereoselectivity Chemical rearrangement
- Keyword (es)
- Aluminio Complejo Aminoester Benzaldehído Complejo ariloxi Ciclo 5 eslabones Cicloadición Efecto medio Efecto estérico Heterociclo oxígeno nitrógeno Reacción catalítica Estereoselectividad Transposición química
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06D Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3839890
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
10.1021/jo00078a018 
https://dx.doi.org/10.1021/jo00078a018
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