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Parallel synthesis of 1,2,4-oxadiazoles using CDI activation

Author
DEEGAN, T. L1 ; NITZ, T. J2 ; CEBZANOV, D2 ; PUFKO, D. E2 ; PORCO, J. A1
[1] Argonaut Technologies, 887 Industrial Road, Suite G, San Carlos, CA 94070, United States
[2] Viropharma, Inc., 405 Eagleview Blvd., Exton, PA 19341-1117, United States
Source

Bioorganic & medicinal chemistry letters (Print). 1999, Vol 9, Num 2, pp 209-212 ; ref : 14 ref

ISSN
0960-894X
Scientific domain
Biochemistry, molecular biology, biophysics; Pharmacology drugs
Publisher
Elsevier, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Acylation Amidoxime Cyclodéshydratation DMF Hétérocycle oxygène azote Oxadiazole dérivé Synthèse chimique 1,1p-Carbonyldiimidazole 1,2,4-Oxadiazole(5-[4-méthoxyphényl]-3-[3-(trifluorométhyl)phényl]) Benzohydroximique acide(3-trifluorométhyl) amide Cyclopentanecarboxylique acide
Keyword (en)
Acylation Amidoxime Cyclodehydration N,N-Dimethylformamide Oxygen nitrogen heterocycle Oxadiazole derivatives Chemical synthesis
Keyword (es)
Acilación Amidoxima Ciclodeshidratación Dimetilformamida Heterociclo oxígeno nitrógeno Oxadiazol derivado Síntesis química
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
1684595

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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