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Application of chiral cationic catalysts to several classical syntheses of racemic natural products transforms them into highly enantioselective pathways

Author
HU, Qi-Ying1 ; GANG ZHOU1 ; COREY, E. J1
[1] Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States
Source

Journal of the American Chemical Society. 2004, Vol 126, Num 42, pp 13708-13713, 6 p

CODEN
JACSAT
ISSN
0002-7863
Scientific domain
Biochemistry, molecular biology, biophysics; Chemistry; Organic chemistry; Atomic molecular physics
Publisher
American Chemical Society, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Activité catalytique Addition Diels Alder Catalyse homogène Composé bicyclique Enantiosélectivité Etude expérimentale Hétérocycle oxygène azote bore Réaction catalytique Sélectivité catalyseur 1,3,2-Oxazaborolidinium dérivé
Keyword (en)
Catalyst activity Diels Alder addition Homogeneous catalysis Bicyclic compound Enantioselectivity Experimental study Oxygen nitrogen boron heterocycle Catalytic reaction Catalyst selectivity
Keyword (es)
Actividad catalítica Adición Diels Alder Catálisis homogénea Compuesto bicíclico Enantioselectividad Estudio experimental Heterociclo oxígeno nitrógeno boro Reacción catalítica Selectividad catalizador
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03B Reactivity and mechanisms / 001C03B01 Chemical reactivity

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
16218830

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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