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Application of chiral dipyridylmethane ligands in the enantioselective palladium-catalyzed allylic alkylation

Author
CHELUCCI, Giorgio1 ; CHESSA, Simona1 ; ORRU, Gianmauro1
[1] Dipartimento di Chimica, University di Sassari, via Vienna 2, 07100 Sassari, Italy
Source

Journal of molecular catalysis. A, Chemical. 2004, Vol 220, Num 2, pp 145-151, 7 p ; ref : 27 ref

ISSN
1381-1169
Scientific domain
General chemistry, physical chemistry
Publisher
Elsevier, Amsterdam
Publication country
Netherlands
Document type
Article
Language
English
Author keyword
Allylic alkylation Chiral dipyridylmethane Enantioselectivity Nitrogen heterocycles Palladium complex
Keyword (fr)
Alkylation Composé chiral Coordinat organique Enantiosélectivité Ester Hétérocycle azote Monoterpène Palladium complexe Platinoïde Complexe Réaction catalytique Terpène Acétique acide ester 1,3-diphénylprop-2-ényle Méthane(dipyridyl) dérivé Métal transition Complexe
Keyword (en)
Alkylation Chiral compound Organic ligand Enantioselectivity Ester Nitrogen heterocycle Monoterpene Palladium complex Platinoid Complexes Catalytic reaction Terpene Transition metal Complexes
Keyword (es)
Alquilación Compuesto quiral Ligando orgánico Enantioselectividad Ester Heterociclo nitrógeno Monoterpeno Paladio complejo Platinoide Complejo Reacción catalítica Terpeno Metal transición Complejo
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry / 001C01A Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry / 001C01A03 Catalysis

Discipline
General chemistry and physical chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
16016588

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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