The facile synthesis of 2-bromoindoles via Cs2CO3-promoted intramolecular cyclization of 2-(gem-dibromovinyl)anilines under transition-metal-free conditions

RSC Advances ◽  
2013 ◽  
Vol 3 (1) ◽  
pp. 73-78 ◽  
Author(s):  
Pinhua Li ◽  
Yong Ji ◽  
Wei Chen ◽  
Xiuli Zhang ◽  
Lei Wang
RSC Advances ◽  
2018 ◽  
Vol 8 (50) ◽  
pp. 28637-28641 ◽  
Author(s):  
Yong Liu ◽  
Tao Lu ◽  
Wei-Fang Tang ◽  
Jian Gao

An efficient and practical transition-metal-free synthesis of 2-substituted benzo[b]furans catalyzed by readily accessible base was developed with broad substrates scope.


2021 ◽  
Author(s):  
Xiaoli Huo ◽  
Xiaojuan Chen ◽  
Liya Yu ◽  
Chong Zhang ◽  
Linghui Zeng ◽  
...  

A transition-metal-free, facile and efficient method for the synthesis of 3-alkynylpyrrole-2, 4-dicarboxylates from methylene isocyanides and propiolaldehyde with moderate to good yields has been developed. The direct transformation process and...


2019 ◽  
Vol 17 (2) ◽  
pp. 380-387 ◽  
Author(s):  
Shuai Zou ◽  
Shu Geng ◽  
Lina Chen ◽  
Haitao Wang ◽  
Feng Huang

Visible light driven metal-free intramolecular cyclization: a facile synthesis of 3-position substituted 3,4-dihydroisoquinolin-1(2H)-one.


2018 ◽  
Vol 7 (5) ◽  
pp. 879-882 ◽  
Author(s):  
Dong Wang ◽  
Meng Shen ◽  
Yuxi Wang ◽  
Jianyong Hu ◽  
Junjie Zhao ◽  
...  

Synthesis ◽  
2018 ◽  
Vol 50 (14) ◽  
pp. 2761-2767 ◽  
Author(s):  
Chen Ma ◽  
Huanhuan Liu ◽  
Xinfeng Wang

A novel oxidative amination of sp3 C–H bonds was developed for the efficient synthesis of imidazo[1,5-a]quinolines from readily available α-amino acids and (2-azaaryl)methanes. This domino protocol, which was established in a TBAI-TBHP oxidation system, includes transition-metal-free decarboxylation and intramolecular cyclization. This method represented a new avenue for the synthesis of N-heterocycles using 2-methylquinolines as the synthon of quinoline-2-carbaldehydes.


2021 ◽  
Author(s):  
Ritiele Heck ◽  
Thiago Anjos ◽  
Maira R Giehl ◽  
Ricardo F Schumacher ◽  
Benhur Godoi

Flavone and analogues represent an important class of biologically and pharmacologically active substances commonly found in the composition of diverse plants as part of the class of secondary metabolites. Herein, we have demonstrated an efficient and regioselective synthetic strategy for the preparation of functionalized flavones through sequential demethylation/6-endo-dig intramolecular cyclization of propyn-1-ones, using catalytic amounts of base in the presence of a thiol, by employing NMP as the solvent. The reactions proceeded smoothly under transition-metal-free and open to air conditions, furnishing the desired six-membered heterocycles in moderate to excellent yields, in short reaction time.


2015 ◽  
Vol 56 (24) ◽  
pp. 3777-3781 ◽  
Author(s):  
Chao Huang ◽  
Jia-Hui Guo ◽  
Huang-Mei Fu ◽  
Ming-Long Yuan ◽  
Li-Juan Yang

Author(s):  
Mikhail Feofanov ◽  
Vladimir Akhmetov ◽  
Ryo Takayama ◽  
Konstantin Amsharov

Herein, we describe a facile synthesis of the N-arylated carbazoles via ladderization of fluorinated oligophenylenes. The reaction consists of two subsequent nucleophilic substitutions triggered by the electronic transfer from dimsyl...


2016 ◽  
Vol 14 (47) ◽  
pp. 11148-11153 ◽  
Author(s):  
Jia-hua Chen ◽  
Zi-cong Chen ◽  
Hong Zhao ◽  
Yong Zou ◽  
Xue-jing Zhang ◽  
...  

A facile synthesis of 3,4-disubstituted quinolinones had been developed via KOt-Bu/DMF promoted intramolecular addition of diarylmethanols to α,β-unsaturated amides.


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