Thermal and catalyzed intramolecular Diels-Alder cyclizations of 2,8,10-undecatrienals
- Author
- MARSHALL, J. A1 ; SHEARER, B. G; CROOKS, S. L
[1] Univ. South Carolina, dep. chemistry, Columbia SC 29208, United States - Source
Journal of organic chemistry. 1987, Vol 52, Num 7, pp 1236-1245 ; ref : 17 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 Catalyse acide Composé aliphatique Composé triénique Cyclisation Diastéréosélectivité Effet substituant Enaldéhyde Réaction intramoléculaire Réaction thermique Naphtalènecarbaldéhyde-1(hydroxy-«5» méthyl-«1» octahydro-«1,2,4a,5,6,7,8,8a») Undécatriène-2,8,10al(hydroxy-«7» méthyl-«2»)
- Keyword (en)
- Lewis acid Diels Alder addition Acid catalysis Aliphatic compound Trienic compound Cyclization Diastereoselectivity Substituent effect Enaldehyde Intramolecular reaction Thermal reaction
- Keyword (es)
- Acido Lewis Adición Diels Alder Catálisis ácida Compuesto alifatico Compuesto triénico Ciclizacion Diastereoselectividad Efecto sustituyente Enaldehido Reaccion intramolecular Reacción térmica
- 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
- 8136544
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/jo00383a012 
https://dx.doi.org/10.1021/jo00383a012
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