A metal-free method for facile synthesis of indanones via intramolecular hydroacylation of 2-vinylbenzaldehydes

2021 ◽  
Author(s):  
Guoxue He ◽  
Jinyu Ma ◽  
Jianhui Zhou ◽  
Chunpu Li ◽  
Hong Liu ◽  
...  

A facile method access to indanones was developed under metal- and additive-free conditions in which L-proline served as efficient and environmentally benign catalysts. Compared with previous indanones synthesis by transition-metal-catalyzed...

2022 ◽  
Author(s):  
Wang Xia ◽  
Zi-An Zhou ◽  
Jie Lv ◽  
Shao-Hua Xiang ◽  
Yong-Bin Wang ◽  
...  

N-aryl phenothiazines and phenoxazines are of significant importance in various disciplines throughout academia and industry. Conventional synthetic strategy for the construction of these structures centers on transition-metal-catalyzed cross-coupling of aryl...


RSC Advances ◽  
2016 ◽  
Vol 6 (99) ◽  
pp. 96762-96767 ◽  
Author(s):  
Krishna K. Sharma ◽  
Meenakshi Mandloi ◽  
Neha Rai ◽  
Rahul Jain

A transition metal-catalyzed, environmentally benign, rapid and cost-effective method for the N-(hetero)arylation of zwitterionic amino acids in water is reported.


2017 ◽  
Vol 15 (2) ◽  
pp. 285-300 ◽  
Author(s):  
K. Kubota ◽  
H. Iwamoto ◽  
H. Ito

Recent advances in borylations of organic halides, including both transition-metal-catalyzed and metal-free methods are summarized. Borylative cyclization is also discussed.


2021 ◽  
Author(s):  
Honggui Huang ◽  
Weishuang Li ◽  
Dayou Zhong ◽  
Hu-Chong Wang ◽  
Jing Zhao ◽  
...  

Vicinal trifluoromethyl azides have widespread applications in organic synthesis and drug development. However, their preparation is generally limited to transition-metal-catalyzed three-component reactions. We report a simple and metal-free method that...


2021 ◽  
Author(s):  
Kiran ◽  
Payal Rani ◽  
Sandhya Chahal ◽  
Jayant Sindhu ◽  
Sudhir Kumar ◽  
...  

A gradual shift from metal-catalyzed to metal-free methods is occurring, as the latter are more environmentally benign. This review discusses sustainable protocols for the construction of C–C, C–N, C–P, C–S, and C–O bonds via C–H functionalization of quinoxalin-2(1H)-ones.


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