1607448-87-2Relevant academic research and scientific papers
Access to 3-Sulfonamidoquinolines by Gold-Catalyzed Cyclization of 1-(2′-Azidoaryl)propargylsulfonamides through 1,2- N Migration
Wu, Xiang,Zhao, Li-Ping,Xie, Jin-Ming,Fu, Yan-Ming,Zhu, Cheng-Feng,Li, You-Gui
, p. 801 - 812 (2022/01/03)
We describe a gold-catalyzed cyclization of 1-(2′-azidoaryl)propargylsulfonamides for the synthesis of 3-sulfonamidoquinolines, featuring a rare and highly selective 1,2-N migration. The key α-imino gold carbene intermediate is generated through an intram
Synthesis method of polysubstituted 3-sulfonamide quinoline compound
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Paragraph 0038-0041; 0074-0077, (2021/11/26)
The invention discloses a synthesis method of a polysubstituted 3-sulfonamide quinoline compound, which comprises the following steps: attacking alkynyl by an azide group under the catalysis of gold to form an alpha-imine gold carbene intermediate; and under the action of the alpha-imine intermediate, initiating 1,2-N migration, so as to form the polysubstituted 3-sulfonamide quinoline compound. The synthesis method disclosed by the invention has the advantages of high efficiency, high universality to substrates and the like.
Chiral phosphoric acid-catalyzed asymmetric transfer hydrogenation of quinolin-3-amines
Cai, Xian-Feng,Guo, Ran-Ning,Feng, Guang-Shou,Wu, Bo,Zhou, Yong-Gui
supporting information, p. 2680 - 2683 (2014/06/09)
A chiral phosphoric acid catalyzed asymmetric transfer hydrogenation of aromatic amines, quinolin-3-amines, was successfully developed with up to 99% ee. To supplement our previous work on the Ir-catalyzed asymmetric hydrogenation of 2-alkyl substituted q
