Visible-light driven regioselective synthesis of 1H-tetrazoles from aldehydes through isocyanide-based [3 + 2] cycloaddition

2018 ◽  
Vol 20 (16) ◽  
pp. 3783-3789 ◽  
Author(s):  
Fooleswar Verma ◽  
Anjumala Sahu ◽  
Puneet K. Singh ◽  
Ankita Rai ◽  
Manorama Singh ◽  
...  

A novel and green Co@g-C3N4 catalyzed visible light driven direct regioselective synthesis of 1H-tetrazoles directly from various aldehydes and sodium azide is reported.

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ranjana Aggarwal ◽  
Naman Jain ◽  
Shilpa Sharma ◽  
Prince Kumar ◽  
Gyan Prakash Dubey ◽  
...  

AbstractIn recent times, fused azaheterocycles emerged as impressive therapeutic agents. Binding studies of such azaheterocycles with biomolecules is an important subject for pharmaceutical and biochemical studies aiming at the design and development of new drugs. Fused heterocyclic scaffolds, such as thiazolopyrmidines have long been used in the pharmaceutical industry for the treatment of various diseases. In this study, we have accomplished a regioselective synthesis of 2-aroyl-3-methyl-6,7-dihydro-5H-thiazolo[3,2-a]pyrimidines by the reaction of tetrahydropyrimidine-2(H)-thione with α-bromo-1,3-diketones, generated in situ from 1,3-diketones and NBS, using visible light as an inexpensive, green and renewable energy source under mild reaction conditions with wide-ranging substrate scope. The regioisomer was characterized unambiguously by 2D-NMR [1H-13C] HMBC and [1H-13C] HMQC spectroscopy. In silico toxicity data analysis showed the low toxicity risks of the synthesized compounds. Computational molecular docking studies were carried out to examine the interaction of thiazolo[3,2-a]pyrimidines with calf-thymus DNA (ct-DNA) and Bovine Serum Albumin (BSA). Moreover, different spectroscopic approaches viz. steady-state fluorescence, competitive displacement assay, UV–visible and circular dichroism (CD) along with viscosity measurements were employed to investigate the binding mechanisms of thiazolo[3,2-a]pyrimidines with DNA and BSA. The results thus obtained revealed that thiazolo[3,2-a]pyrimidines offer groove bindings with DNA and showed moderate bindings with BSA.


2019 ◽  
Vol 55 (35) ◽  
pp. 5151-5154 ◽  
Author(s):  
Ayyakkannu Ragupathi ◽  
Arunachalam Sagadevan ◽  
Vaibhav Pramod Charpe ◽  
Chun-Cheng Lin ◽  
Jih-Ru Hwu ◽  
...  

An intuitive visible-light-driven copper-catalyzed process can accomplish regioselective functionalized 3-arylcoumarins via oxidative annulation of simple N-tosylhydrazones with terminal alkynes under O2 (1 atm.) at room temperature.


2020 ◽  
Vol 7 (22) ◽  
pp. 3727-3733
Author(s):  
Han Luo ◽  
Zongyuan Tang ◽  
Tao Wang ◽  
Yi Tian ◽  
Yuan Zhang ◽  
...  

A tuneable and visible-light-driven three-component reaction between N1-sulfonyl-1,2,3-triazoles, saturated heterocycles, and N-bromosuccinimide for regioselective synthesis of N1- or N2-heterocycloalkylated 1,2,3-triazoles.


ACS Omega ◽  
2019 ◽  
Vol 4 (5) ◽  
pp. 7919-7930 ◽  
Author(s):  
Zhongyi Jiao ◽  
Zhendong Liu ◽  
Zhen Ma

Author(s):  
Cheng Cheng ◽  
Dongyun Chen ◽  
Najun Li ◽  
Hua Li ◽  
Qingfeng Xu ◽  
...  

A hollow constructed photocatalyst, In2S3/CdIn2S4, was synthesized for visible-light-driven Cr(vi) reduction.


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