One-pot synthesis of tetrahydro-pyrrolobenzodiazepines and tetrahydro-pyrrolobenzodiazepinones through sequential 1,3-dipolar cycloaddition/N-alkylation (N-acylation)/Staudinger/aza-Wittig reactions

2019 ◽  
Vol 21 (16) ◽  
pp. 4489-4494 ◽  
Author(s):  
Xiaoming Ma ◽  
Xiaofeng Zhang ◽  
John Mark Awad ◽  
Guoshu Xie ◽  
Weiqi Qiu ◽  
...  

A new diastereoselective synthesis of benzodiazepines and diazepinones is developed. This one-pot and three-step synthesis of four components gave two different heterocyclic scaffolds. Green chemistry metrics analysis of the reaction processes provided favorable results.

Author(s):  
Romana Pajkert ◽  
Henryk Koroniak ◽  
Pawel Kafarski ◽  
Gerd Volker Roeschenthaler

A one-pot, regioselective 1,3-dipolar cycloaddition of in situ generated (diethoxyphosphoryl)difluoromethyl nitrile oxide toward selected alkenes and alkynes is reported. This protocol enables facile access to 3,5-disubstituted isoxazolines and isoxazoles bearing...


2009 ◽  
Vol 11 (22) ◽  
pp. 5246-5249 ◽  
Author(s):  
Bor-Cherng Hong ◽  
Rei-Hau Jan ◽  
Chih-Wei Tsai ◽  
Roshan Y. Nimje ◽  
Ju-Hsiou Liao ◽  
...  

2016 ◽  
Vol 22 (4) ◽  
Author(s):  
Khaoula Hajlaoui ◽  
Ahlem Guesmi ◽  
Naoufel Ben Hamadi ◽  
Moncef Msaddek

AbstractReadily prepared copper nanoparticles are an effective catalyst for 1,3-dipolar cycloaddition of carbohydrate azide and a variety of alkynes that furnishes the corresponding 1,2,3-triazole-sucrose derivatives in excellent yields. Products were screened for their antimycobacterial activity against


ChemInform ◽  
2009 ◽  
Vol 40 (30) ◽  
Author(s):  
Lidia S. Konstantinova ◽  
Kirill A. Lysov ◽  
Stanislav A. Amelichev ◽  
Natalia V. Obruchnikova ◽  
Oleg A. Rakitin

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