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The reduction of tertiary N-styrylenamides

Author
AINSCOW, R. B1 ; BRETTLE, R; SHIBIB, S. M
[1] Univ. Sheffield, dep. chemistry, Sheffield S3 7HF, United Kingdom
Source

Journal of the Chemical Society. Perkin transactions. I. 1985, Num 8, pp 1781-1786 ; ref : 20 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)
Acétique acide Ammoniac Carboxamide Composé bicyclique Composé éthylénique Cycle 5 chaînons Etat liquide Hétérocycle azote Lactame Magnésium Méthanol Orientation réaction Réduction chimique Sodium Tétrahydroborate Sodium Stéréoisomère Acétamide(N-benzyl N-styryl) Cyclohexanecarboxylique acide(phénéthyl-2) benzylamide Effet milieu Isoindolinone-1(benzyl-2 benzylidène-3 perhydro) Isoindolinone-1(benzyl-2 benzylidène-3 tétrahydro-3a,4,7,7a) Isoindolinone-1(dibenzyl-2,3 dihydro-4,7) Isoindolinone-1(dibenzyl-2,3 perhydro) Isoindolinone-1(dibenzyl-2,3 tétrahydro-3a,4,7,7a) Isoindolinone-1(dibenzyl-2,3 tétrahydro-4,5,6,7) Pyrrolidone-2(styryl-1)
Keyword (en)
Acetic acid Ammonia Carboxamide Bicyclic compound Ethylenic compound Five membered ring Liquid state Nitrogen heterocycle Lactam Magnesium Methanol Reaction orientation Chemical reduction Sodium Tetrahydroborates Sodium Stereoisomer
Keyword (es)
Magnesio Sodio Sodio
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06B Heterocyclic compounds with only one n hetero atom and condensed derivatives

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
9256327

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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