167960-11-4Relevant articles and documents
Polystyrene-supported recyclable palladacycle catalyst for Heck, Suzuki and Sonogashira reactions
Lin, Chih-An,Luo, Fen-Tair
, p. 7565 - 7568 (2003)
A new type of soluble polystyrene-supported palladium complex as an excellent and recyclable palladacycle catalyst was discovered for carbon-carbon bond formation in Heck, Suzuki and Sonogashira reactions. Precipitation and filtration process for recycling the catalyst was also achieved.
The Catalytic Asymmetric Intermolecular Prins Reaction
Diáz-Oviedo, C. David,Maji, Rajat,List, Benjamin
supporting information, p. 20598 - 20604 (2021/12/14)
Despite their significant potential, catalytic asymmetric reactions of olefins with formaldehyde are rare and metal-free approaches have not been previously disclosed. Here we describe an enantioselective intermolecular Prins reaction of styrenes and paraformaldehyde to form 1,3-dioxanes, using confined imino-imidodiphosphate (iIDP) Br?nsted acid catalysts. Isotope labeling experiments and computations suggest a concerted, highly asynchronous addition of an acid-activated formaldehyde oligomer to the olefin. The enantioenriched 1,3-dioxanes can be transformed into the corresponding optically active 1,3-diols, which are valuable synthetic building blocks.
Preparation of polystyrene-supported soluble palladacycle catalyst for Heck and Suzuki reactions
Luo, Fen-Tair,Xue, Cuihua,Ko, Sheng-Li,Shao, Yu-Der,Wu, Chien-Jung,Kuo, Yang-Ming
, p. 6040 - 6045 (2007/10/03)
A polystyrene-supported palladium complex soluble in tetrahydrofuran and N,N-dimethylacetamide and precipitated in diethyl ether or acetonitrile was prepared from two routes as an excellent and recyclable palladacycle catalyst for carbon-carbon bond formation in Heck and Suzuki reactions to give high yields of the desired products.