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The use of lithium borohydride for deprotecting acetylated alcohols and phenols in the presence of N-acetylated guanidines

Author
HUBER, D1 ; LECLERC, G; ANDERMANN, G
[1] Inst. pharmacologie, Strasbourg 67000, France
Source

Tetrahedron letters. 1986, Vol 27, Num 47, pp 5731-5734 ; ref : 10 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)
Composé benzénique Cycle 5 chaînons Déprotection Guanidines Hétérocycle azote Lithium Chlorure Lithium Tétrahydroborate Sodium Tétrahydroborate Diglyme Imidazolidone-2(acétoxyméthyl-4 diacétyl-«1,3») dichloro-«2p,6p» phénylimine Imidazolidone-2(diacétyl-«1,3» hydroxyméthyl-«4») dichloro-«2p,6p» phénylimine Imidazolidone-2(diacétyl-«1,3»)[acétoxy-«4p» dichloro-«2p,6p»] phénylimine
Keyword (en)
Benzenic compound Five membered ring Deprotection Guanidines Nitrogen heterocycle Lithium Chlorides Lithium Tetrahydroborates Sodium Tetrahydroborates
Keyword (es)
Compuesto bencénico Ciclo 5 eslabones Desprotección Guanidinas Heterociclo nitrógeno Litio Litio Sodio
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06C Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
7940203

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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