Oxazaborolidine catalyzed enantioselective reductions of cyclic meso-imides
- Author
- ROMAGNOLI, R1 ; ROOS, E. C1 ; HIEMSTRA, H1 ; MOOLENAAR, M. J1 ; SPECKAMP, W. N1 ; KAPTEIN, B; SCHOEMAKER, H. E
[1] Univ. Amsterdam, dep. organic chemistry, 1018 WS Amsterdam, Netherlands - Source
Tetrahedron letters. 1994, Vol 35, Num 7 ; 966, 1087-1090 [5 p.]
- CODEN
- TELEAY
- ISSN
- 0040-4039
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Borane Catalyse asymétrique Composé bicyclique Composé méso Enantiosélectivité Hétérocycle azote Réduction chimique 1,3,2-Oxazaborolo [1,2-c] pyrrole(1,1-diphényl-perhydro) Isoindol-1-one(2-benzyl-3-éthoxy-perhydro) Phtalimide(N-benzyl-perhydro)
- Keyword (en)
- Borane Asymmetric catalysis Bicyclic compound Meso compound Enantioselectivity Nitrogen heterocycle Chemical reduction
- Keyword (es)
- Borano Catálisis asimétrica Compuesto bicíclico Compuesto meso Enantioselectividad Heterociclo nitrógeno Reducción química
- 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
- 3963973
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
10.1016/S0040-4039(00)79972-2 
https://dx.doi.org/10.1016/S0040-4039(00)79972-2
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