Visible-Light-Mediated Dearomatization/Cyanation Cascade Reaction of Indoles: Access to Highly Functionalized Spiro-γ-lactam Indolines with Two Contiguous Sterically Congested Quaternary Carbon Stereocenters

2018 ◽  
Vol 360 (15) ◽  
pp. 2879-2884 ◽  
Author(s):  
Qiang Wang ◽  
Yi Qu ◽  
Qing Xia ◽  
Hongjian Song ◽  
Haibin Song ◽  
...  
2021 ◽  
Vol 187 ◽  
pp. 109113
Author(s):  
Xin Zheng ◽  
Jingwei Wang ◽  
Duoduo Xiao ◽  
Huan Chen ◽  
Zhenghuan Lin ◽  
...  

Synthesis ◽  
2018 ◽  
Vol 51 (02) ◽  
pp. 522-529 ◽  
Author(s):  
Deqing Shi ◽  
Lingna Wang ◽  
Tiancong Ma ◽  
Mingming Qiao ◽  
Qiangxian Wu ◽  
...  

A visible-light photoredox-catalyzed oxidation/[3+2] cycloaddition/oxidative aromatization cascade reaction of [(3,4-dihydroisoquinolin-2(1H)-yl)methyl]phosphonates and activated olefins or alkynes for the efficient synthesis of potentially biological active pyrrolo[2,1-a]isoquinoline-substituted phosphonates was developed. This transformation features mild reaction conditions (i.e., visible light irradiation, room temperature), molecular oxygen (O2) as a green oxidant, simple ‘one-pot’ operation.


2017 ◽  
Vol 15 (41) ◽  
pp. 8820-8826 ◽  
Author(s):  
Shangbiao Feng ◽  
Jinlai Li ◽  
Zaimin Liu ◽  
Haiyu Sun ◽  
Hongliang Shi ◽  
...  

The development of a visible-light mediated bromo radical addition/spirocyclization/ester migration cascade reaction to generate 3-bromocoumarins from alkynoates is reported.


2017 ◽  
Vol 53 (33) ◽  
pp. 4585-4588 ◽  
Author(s):  
Shangbiao Feng ◽  
Tao Li ◽  
Chenglong Du ◽  
Peng Chen ◽  
Dengpeng Song ◽  
...  

The development of a visible-light promoted radical insertion/cyclization cascade reaction to generate phenanthridines and isoquinolines from isocyanides under mild reaction conditions is reported.


ChemInform ◽  
2015 ◽  
Vol 46 (38) ◽  
pp. no-no
Author(s):  
Cheng-Wei Lin ◽  
Bor-Cherng Hong ◽  
Wan-Chen Chang ◽  
Gene-Hsiang Lee

Author(s):  
Yuan Huang ◽  
Fanglin Xue ◽  
Hengmao Liu ◽  
Fei Xue ◽  
Xiao-Yu Liu ◽  
...  

Abstract An asymmetric total synthesis of (+)-21-epi-eburnamonine has been achieved. Key features of the synthesis include a visible-light photocatalytic intra-/intramolecular radical cascade reaction to assemble the tetracyclic ABCD ring system, and a highly diastereoselective Johnson-Claisen rearrangement to establish the C20 all-carbon quaternary stereocenter. Graphic Abstract


2019 ◽  
Vol 7 (22) ◽  
pp. 18542-18546 ◽  
Author(s):  
Kuili Zhang ◽  
Rui Ma ◽  
Yanxia Wang ◽  
Zhihao Shi ◽  
Tao Lu ◽  
...  

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