Organocatalytic asymmetric direct alkylation of α-diazoester via C-H bond cleavage
- Author
- URAGUCHI, Daisuke1 ; SORIMACHI, Keiichi1 ; TERADA, Masahiro1
[1] Department of Chemistry, Graduate School of Science, Tohoka University, Sendai 980-8578, Japan - Source
Journal of the American Chemical Society. 2005, Vol 127, Num 26, pp 9360-9361, 2 p ; ref : 15 ref
- CODEN
- JACSAT
- ISSN
- 0002-7863
- Scientific domain
- Biochemistry, molecular biology, biophysics; Chemistry; Organic chemistry; Atomic molecular physics
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Activité catalytique Aldimine Catalyse homogène Composé diazoïque Enantiosélectivité Etude expérimentale Mécanisme réaction Réaction Friedel Crafts Réaction asymétrique Réaction catalytique Sélectivité catalyseur Acétique acide(diazo) ester éthyle Arènecarbaldéhyde aroylimine Phosphorique acide dérivé
- Keyword (en)
- Catalyst activity Aldimine Homogeneous catalysis Diazo compound Enantioselectivity Experimental study Reaction mechanism Friedel Crafts reaction Asymmetric reaction Catalytic reaction Catalyst selectivity
- Keyword (es)
- Actividad catalítica Aldimina Catálisis homogénea Compuesto diazoico Enantioselectividad Estudio experimental Mecanismo reacción Reacción Friedel Crafts Reacción asimétrica Reacción catalítica Selectividad catalizador
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03B Reactivity and mechanisms / 001C03B02 Kinetics and mechanisms
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 16934058
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/ja051922a 
https://dx.doi.org/10.1021/ja051922a
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