Reactions of Aminoacetals with C-Nucleophiles as a New Method for the Synthesis of Di(het)arylmethane Derivatives with a Taurine Fragment

A V Smolobochkin; L J Yakhshilikova; D D Bekrenev; A S Gazizov; A R Burilov; M A Pudovik

doi:10.1134/S1070363222020049

Reactions of Aminoacetals with C-Nucleophiles as a New Method for the Synthesis of Di(het)arylmethane Derivatives with a Taurine Fragment

Russ J Gen Chem. 2022;92(2):161-165. doi: 10.1134/S1070363222020049. Epub 2022 Mar 14.

Authors

A V Smolobochkin¹, L J Yakhshilikova², D D Bekrenev², A S Gazizov¹, A R Burilov¹, M A Pudovik¹

Affiliations

¹ Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, 420088 Kazan, Russia.
² Kazan National Research Technological University, 420015 Kazan, Russia.

Abstract

Based on the acid-catalyzed reaction of functionalized aminoacetals with C-nucleophiles, a series of new diarylmethane derivatives with a taurine fragment were synthesized, the structure of which was established by NMR spectroscopy method.

Keywords: C-nucleophiles; diarylmethanes; taurine.