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Total synthesis of oxynitidine via lithiated toluamide-imine cycloaddition

Author
CLARK, R. D1 ; JAHANGIR
[1] Syntex Research, Palo Alto CA 94304, United States
Source

Journal of organic chemistry. 1988, Vol 53, Num 10, pp 2378-2381 ; ref : 17 ref

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)
Acétal Alcaloïde Aldimine Carboxamide Composé aromatique Composé pentacyclique Condensation chimique Cycloaddition Hétérocycle oxygène azote Lactame Lithiation Acétaldéhyde(bromo) diméthylacétal Benzodioxole-1,3carbaldéhyde-5,méthylimine Benzodioxolo phénanthridine dérivé Isoquinoléineacétique-4 acide([benzodioxole-«1,3»yl-«5»]-«3» diméthoxy-«6,7» méthyl-«2» oxo-«1» tétrahydro-«1,2,3,4») Oxiranne Oxynitidine «o»-Toluique acide(diméthoxy-«4,5») diéthylamide
Keyword (en)
Acetal Alkaloid Aldimine Carboxamide Aromatic compound Pentacyclic compound Condensation reaction Cycloaddition Oxygen nitrogen heterocycle Lactam Lithiation
Keyword (es)
Acetal Alcaloide Aldimina Carboxamida Compuesto aromático Compuesto pentacíclico Condensación química Cicloadición Heterociclo oxígeno nitrógeno Lactamo Litiación
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06D Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
7144149

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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