Ruthenium-catalyzed oxidative C-H alkenylation of aryl carbamates
A cationic ruthenium(ii) catalyst enabled highly efficient oxidative alkenylations of electron-rich arenes bearing removable, weakly coordinating carbamates, and allowed for cross-dehydrogenative C-H bond functionalization in an aerobic manner. This journ
Li, Jie,Kornhaass, Christoph,Ackermann, Lutz
supporting information
p. 11343 - 11345,3
(2012/12/12)
Intramolecular acylation during acid chloride formation of some o-styryl phenoxyacetic acids
o-Isopropenyl phenoxyacetic acids 1 and 8 on treatment with thionyl chloride followed by aqueous workup furnished the acylated products 4 and 9 in moderate yields. The corresponding acid chlorides could also be cyclised with stannic chloride. The acid chl
Biswas,Ghosh,Venkateswaran
p. 1865 - 1874
(2007/10/02)
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