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Diels-Alder reactions of cycloalkenones. XI: Regioselectivity of 2-cyclohexenones

Author
ANGELL, E. C1 ; FRINGUELLI, F; MINUTI, L; PIZZO, F; TATICCHI, A; WENKERT, E
[1] Univ. studi, dip. chimica, Perugia 06100, Italy
Source

Journal of organic chemistry. 1986, Vol 51, Num 26, pp 5177-5182 ; ref : 14 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)
Acide Lewis Addition Diels Alder Composé aliphatique Composé bicyclique Composé diénique Composé insaturé Composé monocyclique Enone Réaction catalytique Régiosélectivité Stéréoisomère Cyclohexène-«2»one(diméthyl-«5,5») Cyclohexène-«2»one(triméthyl-«2,6,6») Isoprène Naphtalénone-1(octahydro-«1,2,3,4,4a,5,7,7a» triméthyl-«3,3,6») Pentadiène-1,3(méthyl-«2»)
Keyword (en)
Lewis acid Diels Alder addition Aliphatic compound Bicyclic compound Dienic compound Unsaturated compound Monocyclic compound Enone Catalytic reaction Regioselectivity Stereoisomer
Keyword (es)
Acido Lewis Adición Diels Alder Compuesto alifatico Compuesto bicíclico Compuesto diénico Compuesto insaturado Compuesto monocíclico Enona Reacción catalítica Regioselectividad Estereoisomero
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05A Alicyclic compounds

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
8175975

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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