mannich cyclization
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2022 ◽  
Author(s):  
Bei-Bei Zhang ◽  
Shuo Peng ◽  
Feiyi Wang ◽  
Cuifen Lu ◽  
Junqi Nie ◽  
...  

An unprecedented redox-neutral annulation of tertiary anilines with electron-deficient alkynes was developed that proceeds through a cascade Friedel-Crafts alkylation/[1,5]-hydride transfer/Mannich cyclization sequence. Under B(C6F5)3 catalysis, a range of functionalized 1,2,3,4-tetrahydroquinolines...


Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3617
Author(s):  
Yueteng Zhang ◽  
Peng Ji ◽  
Xiang Meng ◽  
Feng Gao ◽  
Fanxun Zeng ◽  
...  

A simple arylamine-catalyzed Mannich-cyclization cascade reaction was developed for facile synthesis of substituted 2H-benzo[h]chromenes. The notable feature of the process included the efficient generation of ortho-quinone methides (o-QMs) catalyzed by a simple aniline. The mild reaction conditions allowed for a broad spectrum of 1- and 2-naphthols and trans-cinnamaldehydes to engage in the cascade sequence with high efficiency.


2020 ◽  
Vol 11 (22) ◽  
pp. 5716-5723 ◽  
Author(s):  
Egor M. Larin ◽  
Joachim Loup ◽  
Iuliia Polishchuk ◽  
Rachel J. Ross ◽  
Andrew Whyte ◽  
...  

Copper-catalyzed enantio- and diastereoselective conjugate borylation across Michael acceptors, with subsequent Mannich-type cyclization, was utilized to construct tetrahydroquinoline scaffolds containing three contiguous stereocenters.


2018 ◽  
Vol 16 (25) ◽  
pp. 4641-4649 ◽  
Author(s):  
Mei-Xin Zhao ◽  
Zhi-Wen Dong ◽  
Guang-Yu Zhu ◽  
Xiao-Li Zhao ◽  
Min Shi

This reaction provides facile access to a variety of optically active imidazoline-fused sulfahydantoin derivatives in excellent yields and good to excellent stereoselectivities.


2017 ◽  
Vol 359 (24) ◽  
pp. 4267-4273 ◽  
Author(s):  
Wenzhong Zhang ◽  
Xin Wang ◽  
Biqing Zhu ◽  
Di Zhu ◽  
Jianlin Han ◽  
...  

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