Heck reaction with heteroaryl halides in the presence of a palladium-tetraphosphine catalyst
- 17 July 2002
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 43 (32) , 5625-5628
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- A new efficient tetraphosphine/palladium catalyst for the Heck reaction of aryl halides with styrene or vinylether derivativesTetrahedron Letters, 2002
- Palladium/Tetraphosphine Catalysed Heck Reaction with ortho-Substituted Aryl BromidesSynlett, 2001
- Efficient Heck Vinylation of Aryl Halides Catalyzed by a New Air-Stable Palladium−Tetraphosphine ComplexThe Journal of Organic Chemistry, 2001
- A New Tetratertiary Phosphine Ligand and Its Use in Pd-Catalyzed Allylic SubstitutionThe Journal of Organic Chemistry, 2001
- Palladium–tetraphosphine catalysed cross coupling of aryl bromides with arylboronic acids: remarkable influence of the nature of the ligandChemical Communications, 2001
- Dramatic acceleration of the catalytic process of the amination of allyl acetates in the presence of a tetraphosphine/palladium systemChemical Communications, 2000
- SYNTHESIS OF POLYPODAL DIPHENYLPHOSPHINE LIGANDS. A REVIEWOrganic Preparations and Procedures International, 1999
- Palladacycles: Efficient New Catalysts for the Heck Vinylation of Aryl HalidesChemistry – A European Journal, 1997
- Studies on pyrimidine derivatives. XXX. The palladium-catalyzed cross-coupling reaction of iodopyrimidines with terminal olefinic compounds.Chemical and Pharmaceutical Bulletin, 1982