Oxidative versus vicarious nucleophilic substitution of hydrogen in the reaction of dithiane derivatives with nitroarenes
- Author
- MAKOSZA, M; SYPNIEWSKI, M
Polish acadd. sci., inst. organic chemistry, 01-224 Warsaw, Poland - Source
Tetrahedron (Oxford. Print). 1994, Vol 50, Num 16 ; X, 4913-4920 [9 p.] ; ref : 20 ref
- CODEN
- TETRAB
- ISSN
- 0040-4020
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Alkylation Composé benzénique Composé nitro Effet substituant Halogène Composé organique Réactivité chimique Substitution aromatique Substitution nucléophile 1,3-Dithiane-1,1-dioxyde 1,3-Dithianium(1-alkyl) 1,3-Dithione(2-[5-halogéno-2-nitrophényl])-1,1-dioxyde Benzène(1-halogéno-4-nitro) Benzène(2-[(3-[alkylthio] propylthio) méthyl]-4-halogéno-1-nitro)
- Keyword (en)
- Alkylation Benzenic compound Nitro compound Substituent effect Halogen Organic compounds Chemical reactivity Aromatic substitution Nucleophilic substitution
- Keyword (es)
- Alquilación Compuesto bencénico Compuesto nitro Efecto sustituyente Halógeno Compuesto orgánico Reactividad química Sustitución aromática Substitución nucleófila
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C03 Noncondensed benzenic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4052731
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)85026-2 
https://dx.doi.org/10.1016/S0040-4020(01)85026-2
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