Ni(II) Tol-BINAP-catalyzed enantioselective orthoester alkylations of N-acylthiazolidinethiones
- Author
- EVANS, David A1 ; THOMSON, Regan J1
[1] Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States - Source
Journal of the American Chemical Society. 2005, Vol 127, Num 30, pp 10506-10507, 2 p ; ref : 17 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 Alkylation Catalyseur complexe Coordinat organique Cycle 5 chaînons Enantiosélectivité Etude expérimentale Hétérocycle soufre azote Nickel Complexe Phosphine ditertiaire Réaction asymétrique Réaction catalytique Sélectivité catalyseur Thiazolidine-2-thione(3-acyl) Métal transition Complexe
- Keyword (en)
- Catalyst activity Alkylation Complex catalyst Organic ligand Five membered ring Enantioselectivity Experimental study Sulfur nitrogen heterocycle Nickel Complexes Ditertiary phosphine Asymmetric reaction Catalytic reaction Catalyst selectivity Transition metal Complexes
- Keyword (es)
- Actividad catalítica Alquilación Catalizador complejo Ligando orgánico Ciclo 5 eslabones Enantioselectividad Estudio experimental Heterociclo azufre nitrógeno Niquel Complejo Fosfina diterciaria Reacción asimétrica Reacción catalítica Selectividad catalizador Metal transición Complejo
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03B Reactivity and mechanisms / 001C03B01 Chemical reactivity
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 17021308
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/ja053386s 
https://dx.doi.org/10.1021/ja053386s
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