65189-93-7Relevant academic research and scientific papers
Fast oxidation of secondary alcohols by the bromate-bromide system using cyclic microwave heating in acidic water
P??kk?nen, Sanna,Pursiainen, Jouni,Lajunen, Marja
scheme or table, p. 6695 - 6699 (2011/02/23)
We report an improved, gentle, cyclic microwave activation technique for the oxidation of secondary alcohols using nonhazardous hypobromous acid (BrOH) as the reagent in acidic water. Several aliphatic and aromatic secondary alcohols were successfully oxidized to the corresponding ketones using this technique in high yields and with only minor amounts of side products.
Polystyrene-supported palladacycle catalysts
-
Page/Page column 3; 4, (2010/02/15)
This invention relates to a recyclable palladacycle catalyst of formula in which each is a single bond or a double bond, provided that if one is a double bond, its neighboring is not a double bond; each of X and Z, independently, is —P(R′)—, —S—, —N(R′)—,
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.
Polystyrene-supported recyclable palladacycle catalyst for Heck, Suzuki and Sonogashira reactions
Lin, Chih-An,Luo, Fen-Tair
, p. 7565 - 7568 (2007/10/03)
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.
