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Cerium chloride-promoted nucleophilic addition of Grignard reagents to ketones an efficient method for the synthesis of tertiary alcohols

Author
IMAMOTO, T; TAKIYAMA, N; NAKAMURA, K
Chriba univ., fac. sci., dep. chemistry
Source

Tetrahedron letters. 1985, Vol 26, Num 39, pp 4763-4766 ; ref : 9 ref

CODEN
TELEAY
ISSN
0040-4039
Scientific domain
Biochemistry, molecular biology, biophysics; Organic chemistry
Publisher
Elsevier, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Addition nucléophile Alcool tertiaire Composé aliphatique Composé allylique Composé aromatique Composé benzénique Composé bicyclique Composé homoallylique Composé monocyclique Composé saturé Cyclohexène-2ol(isopropyl-1) Cyclohexène-2one Cyclopentanol(isopropyl-1) Cyclopentanone Cyclopentène-2one Cyclopentène-3ol(phényl-1) Cérium III Chlorure Cétone Enone Heptanol-3(benzyl-3 phényl-1) Naphtalénone-2(tétrahydro-1,2,3,4) Naphtol-2(éthyl-2 tétrahydro-1,2,3,4) Pentanone-3(diméthyl-2,4) Pentanone-3(diphényl-1,5) Pentène-1ol-3(benzyl-3 phényl-5) Réactif Grignard
Keyword (en)
Nucleophilic addition Tertiary alcohol Aliphatic compound Allylic compound Aromatic compound Benzenic compound Bicyclic compound Homoallylic compound Monocyclic compound Saturated compound Cerium III Chlorides Ketone Enone Grignard reagent
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
8468752

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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