158503-49-2Relevant articles and documents
Direct arylation of substituted pyridines with arylboronic acids catalyzed by iron(II) oxalate
Huang, Yibo,Guan, Dan,Wang, Liang
, p. 1294 - 1298 (2015/02/05)
The direct arylation of substituted pyridines with several arylboronic acids has been developed. This transformation could proceed readily at ambient temperature using inexpensive reagents: iron(II) oxalate as a catalyst, potassium persulfate as a co-oxidant, which can afford the arylated products in mild to good yields. The mechanism is presumed to proceed through a nucleophilic radical addition to the pyridines with in situ reoxidation.
SYNTHESIS AND BIOLOGICAL ACTIVITIES OF NEW HMG-COA SYNTHASE INHIBITORS: 2-OXETANONES WITH A SIDE CHAIN CONTAINING BIPHENYL, TERPHENYL OR PHENYLPYRIDINE
Hashizume, Hirokazu,Ito, Hajime,Kanaya, Naoaki,Nagashima, Hajime,Usui, Hiroyuki,et al.
, p. 1551 - 1572 (2007/10/02)
A series of 1233A analogs containing biphenylyl, terphenylyl or phenylpyridyl groups in their side chain were synthesized and tested for the inhibitory activities against 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase and inhibition for the chol
