5317-80-6Relevant articles and documents
Iron-Catalyzed Electrophilic Amination of Sodium Sulfinates with Anthranils
Liang, Baihui,Huang, Junjie,Zhu, Weidong,Li, Yawen,Jiang, Lanping,Gao, Yang,Xie, Feng,Li, Yibiao,Chen, Xiuwen,Zhu, Zhongzhi
, p. 1466 - 1473 (2021/02/09)
A practical method for the synthesis of N-(2-carbonylaryl) benzenesulfonamides via an iron-catalyzed electrophilic amination of sodium sulfinates with anthranils is described. This redox-neutral transformation has high atom efficiency and is achieved under simple and mild reaction conditions. A wide range of anthranils and sodium sulfinates were compatible in this transformation. Moreover, the synthetic potential of this methodology was further demonstrated by the synthesis of various useful N-heterocycles and derivatives.
Diastereoselective synthesis of 2,4-substituted tetrahydroquinolines via hf(otf)4-catalyzed substitution/cyclization of 2-aminobenzyl alcohols with styrenes
Noji, Masahiro,Kadowaki, Hiroto,Kubota, Yuuki,Yoshida, Tomomi,Saito, Noriko,Yamaguchi, Subaru,Ohata, Ren,Ishii, Keitaro,Takanami, Toshikatsu
, p. 1041 - 1073 (2017/07/27)
An efficient and convenient stereoselective synthetic approach to 2,4-substituted 1,2,3,4-tetrahydroquinoline has been developed. This catalytic procedure involves a sequential reaction of 2-aminobenzyl alcohol with styrenes in the presence of Hf(OTf)4 ca
Synthesis and antioxidant activity of a new series of 2,1-benzothiazine 2,2-dioxide hydrazine derivatives
Shafiq, Muhammad,Khan, Islam Ullah,Zia-Ur-Rehman, Muhammad,Asghar, Muhammad Nadeem,Asiri, Abdullah M.,Arshad, Muhammad Nadeem
scheme or table, p. 4799 - 4803 (2012/08/08)
A convenient synthesis of a series of new N-benzylidene-N'-(1-ethyl-2, 2-dioxo-2,3-dihydro-1H-2λ6-benzo[c][1,2]thiazin-4-ylidene) -hydrazines is reported. The starting compound methyl anthranilate was reacted with methane sulfonyl chloride, fol
