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Synthesis of tetrasubstituted ozonides by the Griesbaum coozonolysis reaction: Diastereoselectivity and functional group transformations by post-ozonolysis reactions

Author
YUANQING TANG1 ; YUXIANG DONG1 ; KARLE, Jean M2 ; DITUSA, Charles A2 ; VENNERSTROM, Jonathan L1
[1] Department of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, Nebraska 68198-6025, United States
[2] Division of Experimental Therapeutics, Walter Reed Army Institute of Research, Silver Spring, Maryland 20910-7500, United States
Source

Journal of organic chemistry. 2004, Vol 69, Num 19, pp 6470-6473, 4 p

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)
Adamantane Alcool Amine Diastéréosélectivité Ester Ether Groupe fonctionnel Hétérocycle oxygène Oxime Ozonide organique Ozonolyse Stabilité chimique Stéréoisomère cis Sulfone Sulfure organique Synthèse chimique 1,2,4-Trioxolane dérivé Adamantan-2-one oxime dérivé Cyclohexanone dérivé
Keyword (en)
Alcohol Amine Diastereoselectivity Ester Ether Functional group Oxygen heterocycle Oxime Organic ozonide Ozonolysis Chemical stability Cis stereoisomer Sulfone Organic sulfide Chemical synthesis
Keyword (es)
Alcohol Amina Diastereoselectividad Ester Eter Grupo funcional Heterociclo oxígeno Oxima Ozonido orgánico Ozonolisis Estabilidad química Estereoisómero cis Sulfona Sulfuro orgánico Síntesis química
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
16123504

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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