1127335-86-7Relevant academic research and scientific papers
Solvent-free copper-catalyzed oxidative S-arylation of 1,2-diaryldisulfides with aryltrimethoxysilane
Luo, Pei-Song,Yu, Ming,Tang, Ri-Yuan,Zhong, Ping,Li, Jin-Heng
, p. 1066 - 1070 (2009)
A novel and solvent-free protocol for the synthesis of diarylsulfides by the copper-catalyzed oxidative S-arylation of 1,2-diaryldisulfides with aryltrimethoxysilanes is reported. In the presence of CuI, 2-(di-tert-butylphosphino)biphenyl, and TBAF (n-Bu
Substrate-Controlled [5+1] Annulation of 5-Amino-1H-phenylpyrazoles with Alkenes: Divergent Synthesis of Multisubstituted 4,5-Dihydropyrazolo[1,5-a]quinazolines
Jiang, Xunyuan,Wei, Xiaoyi,Lin, Fei,Zhang, Zhixiang,Yao, Guangkai,Yang, Shuai,Zhao, Weijing,Zhao, Chen,Xu, Hanhong
supporting information, p. 3997 - 4003 (2020/06/17)
A new and efficient [5+1] annulation reaction for the first synthesis of 5,5-disubstituted 4,5-dihydropyrazolo[1,5-a]quinazolines is described. This transition-metal-free tandem cyclization was performed with 5-amino-1H-phenylpyrazole and readily availabl
Iron-catalyzed direct sulfenylation and selenylations of phenylpyrazoles: Synthesis of fipronil derivatives with disulfides promoted by a catalytic amount of iodine
Xu, Mei,Zhang, Xiao Hong,Zhong, Ping
experimental part, p. 3472 - 3481 (2012/09/22)
The direct thiolation of phenylpyrazole with disulfide using the FeBr 3/I2 complex as the catalyst in MeCN at 80 °C was reported. With the optimum conditions, several fipronil derivatives of 4-sulfenylpyrazole were synthesized by the reaction of 5-amino-1-[2,6-dichloro- 4-(trifluoromethyl)phenyl-lH-pyrazole-3-arbonitrile (1a) with disulfides (2) in moderate to good yields. The coupling reaction with diaryl diselane also occurred under similar conditions.
Copper-catalyzed selective S-arylation of 1,2-bis(o-amino-1H-pyrazolyl) disulfides with arylboronic acids
Luo, Pei-Song,Wang, Feng,Li, Jin-Heng,Tang, Ri-Yuan,Zhong, Ping
scheme or table, p. 921 - 928 (2009/10/14)
Copper-catalyzed oxidative S-arylation of 1,2-bis(o-amino-1H-pyrazolyl) disulfides with arylboronic acids for the synthesis of (o-amino-1H-pyrazolyl) aryl sulfides has been developed in the presence of CuI, 1,10-phenanthroline, and O2. A variet
