Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jeroen J. H. Diederen"'
Publikováno v:
Advanced Synthesis & Catalysis. 343:255-259
Highly regio- and stereoselective formation of allylamines has been achieved through a three-component reaction between iodobenzene, an allene, and an amine in acetonitrile, catalyzed by in situ formed and by isolated palladium-diphosphine catalysts.
Publikováno v:
Tetrahedron Letters, 40, 4255-4258. Elsevier
Various isoquinolines and pyridines were prepared from aryl- and vinyl halides by a method which involves insertion of an allene into the PdC bond and intramolecular nucleophilic attack of the imine.
Publikováno v:
Tetrahedron Letters. 39:4111-4114
1,1-Dimethylallene inserts into the σ PdC bond of cyclopalladated α-tetralone ketimines leading to stable new heterocycles after depalladation. Intramolecular attack of an imine on a Pd-allyl complex leads to the formation of iminium salts which
Publikováno v:
ChemInform. 29
Publikováno v:
ChemInform. 30
Autor:
J. P. Dorenbos, Jan Reedijk, Jeroen J. H. Diederen, Robert Jochem Heetebrij, Bernhard K. Keppler, Marieke J. Bloemink
Publikováno v:
ChemInform. 30
Publikováno v:
ChemInform. 32
Highly regio- and stereoselective formation of allylamines has been achieved through a three-component reaction between iodobenzene, an allene, and an amine in acetonitrile, catalyzed by in situ formed and by isolated palladium-diphosphine catalysts.
Autor:
Robert J. Heetebrij, J. P. Dorenbos, Jan Reedijk, Jeroen J. H. Diederen, Bernhard K. Keppler, Marieke J. Bloemink
Publikováno v:
European Journal of Inorganic Chemistry. 1999:1655-1657
Publikováno v:
Advanced Synthesis & Catalysis; 2001, Vol. 343 Issue 3, p255-259, 2p