ScholarMate
客服热线:400-1616-289

Access to Polycyclic Thienoindolines via Formal [2+2+1] Cyclization of Alkynyl Indoles with S8 and K2S

Ma, Jinhui; Luo, Jiajun; Jiang, Kai; Zhang, Guangwen*; Liu, Shubin; Yin, Biaolin*
Science Citation Index Expanded
-

摘要

The syntheses of polycyclic thienoindolines bearing a dihydrothiophene or tetrahydrothiophene subunit have not been reported, despite the fact that such compounds may have interesting medicinal properties. Herein, we report a protocol for accessing polycyclic dihydrothiophenes by means of formal [2+2+1] intramolecular dearomatizing cyclization of alkynyl indoles with K2S and S-8 as the sources of sulfide. In addition, tetrahydrothienoindolines were stereoselectively synthesized via a one-pot, two-step protocol involving AgNO3-catalyzed alkenyl dearomatization followed by two nucleophilic addition reactions involving K2S.

关键词

TRISULFUR RADICAL-ANION TETRACYCLIC INDOLINES 3+2 CYCLOADDITION CASCADE REACTIONS C-C ARYLATION CONSTRUCTION ECONOMY SULFUR PYRROLOINDOLINES