The photochemical preparation of ozonides by electron-transfer photo-oxygenation of epoxides
- Author
- SCHAAP, A. P1 ; SHAHABUDDIN SIDDIQUI; GIRIJA PRASAD; PALOMINO, E; SANDISON, M
[1] Wayne state univ., dep. chemistry, Detroit MI 48202, United States - Source
Tetrahedron (Oxford. Print). 1985, Vol 41, Num 11, pp 2229-2235 ; ref : 26 ref
- CODEN
- TETRAB
- ISSN
- 0040-4020
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Cinétique Cycle 3 chaînons Cycle 5 chaînons Epoxyde Etat singulet Fluorescence Hétérocycle oxygène Mécanisme radicalaire Oxygène Oxygénation Ozonide organique Photosensibilisant Réaction photochimique Stéréoisomère Ylure Acétonitrile Anthracènedicarbonitrile-9,10 Biphényle Oxiranne dérivé Trioxolanne-1,2,4 dérivé
- Keyword (en)
- Kinetics Three membered ring Five membered ring Epoxide Singlet state Fluorescence Oxygen heterocycle Radical mechanism Oxygen Oxygenation Organic ozonide Photosensitizer Photochemical reaction Stereoisomer Ylide
- Keyword (es)
- Cinetica
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry / 001C01F Physical chemistry of induced reactions (with radiations, particles and ultrasonics) / 001C01F01 Photochemistry
- Discipline
- General chemistry and physical chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 9254539
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)96597-4 
https://dx.doi.org/10.1016/S0040-4020(01)96597-4
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