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Platinum complex catalyzed reductive N-acylation of nitro compounds

Author
WATANABE, Y1 ; TSUJI, Y; KONDO, T; TAKEUCHI, R
[1] Kyoto univ., fac. eng., dep. hydrocarbon chemistry, Sakyo-ku Kyoto 606, Japan
Source

Journal of organic chemistry. 1984, Vol 49, Num 23, pp 4451-4455 ; ref : dissem

CODEN
JOCEAH
ISSN
0022-3263
Scientific domain
Biochemistry, molecular biology, biophysics; Organic chemistry
Publisher
American Chemical Society, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Acide Lewis Activité catalytique Acylation Acétique acide Amine primaire Carboxamide Complexe chloro Composé aliphatique Composé nitro Composé saturé Intermédiaire réaction Isocyanate organique Nitrène Phosphine tertiaire Platine Complexe Réaction catalytique Réduction chimique Température Acétamide(N-alkyl) Acétamide(N-aryl) Acétamide(N-phényl) Alcane(nitro-1) Benzène(chloro-1 nitro-4) Benzène(nitro) Coordinat organique Triphénylphosphine
Keyword (en)
Lewis acid Catalyst activity Acylation Acetic acid Primary amine Carboxamide Chloro complex Aliphatic compound Nitro compound Saturated compound Reaction intermediate Organic isocyanate Nitrene Tertiary phosphine Platinum Complexes Catalytic reaction Chemical reduction Temperature
Keyword (es)
Actividad catalitica Temperatura
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
8950452

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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