Cyclopropanation of dibenzylaminoacetonitrile: evaluation of 1,2-dibromides and cyclic 1,2-sulfates as dielectrophiles
- Author
- GUILLAUME, D; BRUM-BOUSQUET, M; AITKEN, D. J; HUSSON, H.-P
CNRS fac. sci. pharmaceutiques biologiques, lab. chimie thérapeutique, 75270 Paris, France - Source
Bulletin de la Société chimique de France. 1994, Vol 131, Num 4, pp 391-396 ; ref : 19 ref
- CODEN
- BSCFAS
- ISSN
- 0037-8968
- Scientific domain
- Biochemistry, molecular biology, biophysics; Chemistry
- Publisher
- Elsevier, Paris
- Publication country
- France
- Document type
- Article
- Language
- English
- Keyword (fr)
- Alkylation Composé aliphatique Cycle 5 chaînons Cyclopropanation Enantiosélectivité Etude expérimentale Hydrocarbure bromé Hétérocycle oxygène soufre Mécanisme réaction Nitrile Sulfate organique 1,3,2-Dioxathiolane-2,2-dioxyde(4,5-dialkyl) Acétonitrile(2-dibeuzylamino) Alcane(1,2-dibromo)
- Keyword (en)
- Alkylation Aliphatic compound Five membered ring Cyclopropanation Enantioselectivity Experimental study Bromocarbon Oxygen sulfur heterocycle Reaction mechanism Nitrile Organic sulfate
- Keyword (es)
- Alquilación Compuesto alifático Ciclo 5 eslabones Ciclopropanación Enantioselectividad Estudio experimental Hidrocarburo bromado Heterociclo oxígeno azufre Mecanismo reacción Nitrilo Sulfato orgánico
- 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
- 3454663
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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