X = Y - ZH systems as potential 1,3-dipoles. XXXV: Generation of nitrones from oximes. Class 3 processes. Tandem intramolecular Michael addition (1,3-azaprotio cyclotransfer) : intermolecular 1,3-dipolar cycloaddition reactions
- Author
- GRIGG, R; MARKANDU, J; PERRIOR, T; SIVAGNANASUNDRAM SURENDRAKUMAR; WARNOCK, W. J
Leeds univ., school chemistry, Leeds West Yorks. LS2 9JT, United Kingdom - Source
Tetrahedron (Oxford. Print). 1992, Vol 48, Num 33, pp 6929-6952 ; ref : 33 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 Michaël Composé éthylénique Cycloaddition dipolaire 1,3 Mécanisme réaction Nitrone Réaction concertée Réaction thermique Acétone oxime Amine(isopropylidène 1,1,2-triméthylpropyl) oxyde But-2-ène(2,3-diméthyl) Réaction tandem
- Keyword (en)
- Michael addition Ethylenic compound 1,3-Dipolar cycloaddition Reaction mechanism Nitrone Concerted reaction Thermal reaction Tandem reaction
- Keyword (es)
- Adición Michael Compuesto etilénico 1,3-Dipolar cicloadición Mecanismo reacción Nitrona Reacción concertada Reacción térmica
- 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
- 5564741
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)89883-5 
https://dx.doi.org/10.1016/S0040-4020(01)89883-5
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