Theoretical reaction paths for cation radical cycloadditions: the [3+2] or role-reversed cation radical Diels-Alder
- Author
- BELLVILLE, D. J1 ; BAULD, N. L
[1] Univ. Texas, dep. chemistry, Austin TX 78712, United States - Source
Tetrahedron (Oxford. Print). 1986, Vol 42, Num 22, pp 6167-6173 ; ref : 36 ref
- CODEN
- TETRAB
- ISSN
- 0040-4020
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Addition Diels Alder Composé bicyclique Composé diénique conjugué Cycloaddition Hydrocarbure Méthode MINDO 3 Méthode ab initio Radical libre organique cationique Butadiène-1,3 Ethyléniumyle
- Keyword (en)
- Diels Alder addition Bicyclic compound Conjugated dienic compound Cycloaddition Hydrocarbon MINDO 3 method Ab initio method Organic radical cation
- Keyword (es)
- Adición Diels Alder Compuesto bicíclico Compuesto diénico conjugado Cicloadición Hidrocarburo Método MINDO 3 Método ab initio Radical libre orgánico catiónico
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03B Reactivity and mechanisms / 001C03B04 Free radicals chemistry
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 8162969
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
10.1016/S0040-4020(01)88077-7 
https://dx.doi.org/10.1016/S0040-4020(01)88077-7
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