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The activating effects of arylazo groups on a double bond. Preparation and properties of some bis(dialkylamino)arylazoethenes and related compounds

Author
GILCHRIST, T. L1 ; STEVENS, J. A; PARTON, B
[1] Robert Robinson Laboratories, Liverpool L69 3BX, United Kingdom
Source

Journal of the Chemical Society. Perkin transactions. I. 1985, Num 8, pp 1737-1740 ; 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)
Aminal Amine Chlore Composé organique Composé benzénique Composé conjugué Composé géminé Effet substituant Orthoester Réactivité Spectre IR Spectre RMN Spectre UV visible Tautomérie azo hydrazono Thioester Thiol Cétène dérivé Diazène(aryl dichloro-2,2 vinyl) Diazène(bis-dialkylamino-2,2 vinyl dinitro-2,4 phényl) Hydrogène 1 Orthoacétique acide(dinitro-2p,4p phénylhydrazono) ester tris-[chloro-4 phényle] Trithioorthoacétique acide(dinitro-2p,4p phénylhydrazono) ester triphényle
Keyword (en)
Aminal Amine Chlorine Organic compounds Benzenic compound Conjugated compound Geminal compound Substituent effect Orthoester Reactivity Infrared spectrum NMR spectrum Ultraviolet visible spectrum Azo hydrazono tautomerism Thioester Thiol
Keyword (es)
Cloro
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
9248344

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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