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Reactions of nitroso hetero-Diels-Alder cycloadducts with azides : Stereoselective formation of triazolines and aziridines

Author
BODNAR, Brian S1 ; MILLER, Marvin J1 2
[1] Department of Chemistry and Biochemistry, University of Notre Dame, 251 Nieuwland Science Hall, Notre Dame, Indiana 46556, United States
[2] Leibniz-Institute for Natural Product Research and Infection Biology, Hans Knöll Institute, Beutenbergstrasse 11a, 07745 Jena, Germany
Source

Journal of organic chemistry. 2007, Vol 72, Num 10, pp 3929-3932, 4 p ; ref : 30 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)
Alcène Azide Aziridine dérivé Composé nitroso Composé éthylénique Hétérocycle azote Hétérocycle oxygène azote Stéréosélectivité Triazole dérivé 6-Oxa-3,7-diazatricyclo[3.2.1.02,4]octane dérivé Addition hétéro Diels Alder Cyclopentadiène dérivé
Keyword (en)
Alkene Organic azide Aziridine derivatives Nitroso compound Ethylenic compound Nitrogen heterocycle Oxygen nitrogen heterocycle Stereoselectivity Triazole derivatives
Keyword (es)
Alqueno Azida orgánica Compuesto nitroso Compuesto etilénico Heterociclo nitrógeno Heterociclo oxígeno nitrógeno Estereoselectividad Triazol derivado
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
18747084

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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