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A theoretical study of favorskii reaction stereochemistry. Lessons in torquoselectivity

Author
HAMBLIN, Graham D1 ; JIMENEZ, Raphael P1 ; SORENSEN, Ted S1
[1] Department of Chemistry, University of Calgary, Calgary, Alberta T2N 1N4, Canada
Source

Journal of organic chemistry. 2007, Vol 72, Num 21, pp 8033-8045, 13 p ; ref : 43 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)
Analogue Conformation Cyclisation Energie transition Enolate Etat fondamental Etat transition Etude expérimentale Etude théorique Mécanisme SN1 Mécanisme SN2 Mécanisme réaction Méthode ab initio Réaction concertée Rétention configuration Simulation Solvant polaire Solvatation Structure moléculaire Stéréochimie Transposition Favorsky Transposition chimique Cyclopropanone dérivé
Keyword (en)
Analog Conformation Cyclization Transition energy Enolate Ground state Transition state Experimental study Theoretical study SN1 mechanism SN2 mechanism Reaction mechanism Ab initio method Concerted reaction Configuration retention Simulation Polar solvent Solvation Molecular structure Stereochemistry Favorsky rearrangement Chemical rearrangement
Keyword (es)
Análogo Conformación Ciclización Energía transición Enolato Estado fundamental Estado transitorio Estudio experimental Estudio teórico Mecanismo SN1 Mecanismo SN2 Mecanismo reacción Método ab initio Reacción concertada Retención configuración Simulación Disolvente polar Solvatación Estructura molecular Estereoquímica Transposición Favorsky Transposición química
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
19203724

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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