Organic heterocyclothiazenes. XVIII : 1,3,2-dithiazolium salts and 1,3,2-dithiazolethiones
- Author
- GRAY, M. A; REES, C. W
Imperial coll. sci. technology medicine, dep. chemistry, London SW7 2AY, United Kingdom - Source
Journal of the Chemical Society. Perkin transactions. I. 1993, Num 24, pp 3077-3080 ; ref : 11 ref
- CODEN
- JCPRB4
- ISSN
- 0300-922X
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- Royal Society of Chemistry, Cambridge
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Azide Cation organique Cycle 5 chaînons Cyclisation Halogénure sulfényle Hétérocycle soufre azote Réactivité chimique Thione λ4-Sulfane organique 1,3,2-Dithiazol-1-ium chlorure 1,3,2-Dithiazol-1-ium(5-chloro) chlorure 1S↑IV,3,2-Dithiazol-4-one Ethane-1,2-disulfénique acide(chloro) dichlorure Ethane-1,2-disulfénique acide(dichloro) dichlorure Silane(azido triméthyl)
- Keyword (en)
- Organic azide Organic cation Five membered ring Cyclization Sulfenyl halide Sulfur nitrogen heterocycle Chemical reactivity Thione Organic λ4-sulfane
- Keyword (es)
- Azida orgánica Catión orgánico Ciclo 5 eslabones Ciclización Halogenuro sulfenilo Heterociclo azufre nitrógeno Reactividad química Tiona Sulfurano orgánico
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06D Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3901066
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
10.1039/p19930003077 
https://dx.doi.org/10.1039/p19930003077
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