The development of original methodologies of directed synthesis of le-Carbs their analogs and precursors base donacetylene and its derivatives

Author(s):  
Б. Трофимов ◽  
B. Trofimov ◽  
Н. Гусарова ◽  
N. Gusarova

New reactions, which have been discovered and continue to be developed in A.E. Favorsky Irkutsk institute of chemistry SB RAS on the basis of acetylene, a product of oil, gas and coal processing and multi-faceted building block for organic synthesis, have been considered. These reactions provide for the shortest routes to construction of fundamental heterocyclic scaffolds (pyrroles, imidazoles, pyrazoles, indoles, pyridines, dihydropyridines, etc.) with desirable and optimum combination of functional pharmacophoric groups and fragments, which are responsible for antiviral (HIV, flu), antitumor, tuberculostatic and hypotensive activities.

Synthesis ◽  
2022 ◽  
Author(s):  
Dishu Zeng ◽  
Tianbao Yang ◽  
Niu Tang ◽  
Wei Deng ◽  
Jiannan Xiang ◽  
...  

A simple, mild, green and efficient method for the synthesis of 2-aminobenzamides was highly desired in organic synthesis. Herein, we developed an efficient, one-pot strategy for the synthesis of 2-aminobenzamides with high yields irradiated by UV light. 32 examples proceeded successfully by this photo-induced protocol. The yield reached up to 92%. The gram scale was also achieved easily. This building block could be applied in the preparation of quinazolinones derivatives. Amino acid derivatives could be employed smoothly at room temperature. Finally, a plausible mechanism was proposed.


2014 ◽  
Vol 998-999 ◽  
pp. 15-18
Author(s):  
Сhao Hong Dong ◽  
Zhou Lu ◽  
Ping Zhu ◽  
Lei Wang

A novel building block in organic synthesis, poly (4-iodobutoxylmethylsiloxane)(PIBMS) with high reaction activity was prepared by poly (hydromethylsiloxane)(PHMS), methyl iodide and tetrahydrofuran (THF) in the presence of a catalytic amount of PdCl2. The structure of PIBMS was characterized by the FT-IR and NMR spectra. The reaction conditions were optimized.


ChemInform ◽  
2005 ◽  
Vol 36 (23) ◽  
Author(s):  
Dieter Enders ◽  
Matthias Voith ◽  
Achim Lenzen

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