One-pot synthesis of 1,5-benzodiazepine-2,3-dicarboxylates via three-component domino reactions in the presence of γ-Fe2O3@SiO2/Ce(OTf)3

2021 ◽  
Vol 57 (7-8) ◽  
pp. 806-816
Author(s):  
Xiaoying An ◽  
Lei Gao ◽  
Mingliang Wang ◽  
Haitao Wu ◽  
Lanzhi Wang
2016 ◽  
Vol 42 (6) ◽  
pp. 5915-5926 ◽  
Author(s):  
Razieh Mohebat ◽  
Afshin Yazdani Elah Abadi ◽  
Malek-Taher Maghsoodlou ◽  
Mohsen Mohammadi

2009 ◽  
Vol 74 (20) ◽  
pp. 7618-7626 ◽  
Author(s):  
Chan Woo Huh ◽  
Gagandeep K. Somal ◽  
Christopher E. Katz ◽  
Huaxing Pei ◽  
Yibin Zeng ◽  
...  

2020 ◽  
Vol 44 (25) ◽  
pp. 10428-10440
Author(s):  
Hai-tao Wu ◽  
Lan-zhi Wang

Unique green-chemistry approaches have been developed for the one-pot synthesis of two series of novel 1,5-benzodiazepines 4 and 5.


2018 ◽  
Vol 42 (24) ◽  
pp. 20032-20040 ◽  
Author(s):  
Yue-Wei Sun ◽  
Lan-Zhi Wang

A simple and highly efficient protocol for the one-pot synthesis of novel benzodiazepines, which fused tricyclic or tetracyclic systems containing aryl, carboxyl, ester and acyl groups, was developed. Libraries of 40 new compounds were successfully synthesized via three-component or domino reactions by using a mild catalyst (γ-Fe2O3@SiO2/CeCl3) in good to excellent yields (82–97%).


RSC Advances ◽  
2015 ◽  
Vol 5 (30) ◽  
pp. 23291-23302 ◽  
Author(s):  
Koorathota Suman ◽  
Sathiah Thennarasu

A method for construction of three classes of densely functionalized dispirocyclopentaneoxindoles with multiple chiral stereocenters is developed using base promoted self-domino and domino reactions with/without the presence of nucleophilic solvents.


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