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

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.

Detalles Bibliográficos
Autores principales: Smolobochkin, A. V., Yakhshilikova, L. J., Bekrenev, D. D., Gazizov, A. S., Burilov, A. R., Pudovik, M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pleiades Publishing 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921706/
https://www.ncbi.nlm.nih.gov/pubmed/35308085
http://dx.doi.org/10.1134/S1070363222020049
_version_ 1784669379050340352
author Smolobochkin, A. V.
Yakhshilikova, L. J.
Bekrenev, D. D.
Gazizov, A. S.
Burilov, A. R.
Pudovik, M. A.
author_facet Smolobochkin, A. V.
Yakhshilikova, L. J.
Bekrenev, D. D.
Gazizov, A. S.
Burilov, A. R.
Pudovik, M. A.
author_sort Smolobochkin, A. V.
collection PubMed
description 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.
format Online
Article
Text
id pubmed-8921706
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Pleiades Publishing
record_format MEDLINE/PubMed
spelling pubmed-89217062022-03-15 Reactions of Aminoacetals with C-Nucleophiles as a New Method for the Synthesis of Di(het)arylmethane Derivatives with a Taurine Fragment Smolobochkin, A. V. Yakhshilikova, L. J. Bekrenev, D. D. Gazizov, A. S. Burilov, A. R. Pudovik, M. A. Russ J Gen Chem Article 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. Pleiades Publishing 2022-03-14 2022 /pmc/articles/PMC8921706/ /pubmed/35308085 http://dx.doi.org/10.1134/S1070363222020049 Text en © Pleiades Publishing, Ltd. 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Smolobochkin, A. V.
Yakhshilikova, L. J.
Bekrenev, D. D.
Gazizov, A. S.
Burilov, A. R.
Pudovik, M. A.
Reactions of Aminoacetals with C-Nucleophiles as a New Method for the Synthesis of Di(het)arylmethane Derivatives with a Taurine Fragment
title Reactions of Aminoacetals with C-Nucleophiles as a New Method for the Synthesis of Di(het)arylmethane Derivatives with a Taurine Fragment
title_full Reactions of Aminoacetals with C-Nucleophiles as a New Method for the Synthesis of Di(het)arylmethane Derivatives with a Taurine Fragment
title_fullStr Reactions of Aminoacetals with C-Nucleophiles as a New Method for the Synthesis of Di(het)arylmethane Derivatives with a Taurine Fragment
title_full_unstemmed Reactions of Aminoacetals with C-Nucleophiles as a New Method for the Synthesis of Di(het)arylmethane Derivatives with a Taurine Fragment
title_short Reactions of Aminoacetals with C-Nucleophiles as a New Method for the Synthesis of Di(het)arylmethane Derivatives with a Taurine Fragment
title_sort reactions of aminoacetals with c-nucleophiles as a new method for the synthesis of di(het)arylmethane derivatives with a taurine fragment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921706/
https://www.ncbi.nlm.nih.gov/pubmed/35308085
http://dx.doi.org/10.1134/S1070363222020049
work_keys_str_mv AT smolobochkinav reactionsofaminoacetalswithcnucleophilesasanewmethodforthesynthesisofdihetarylmethanederivativeswithataurinefragment
AT yakhshilikovalj reactionsofaminoacetalswithcnucleophilesasanewmethodforthesynthesisofdihetarylmethanederivativeswithataurinefragment
AT bekrenevdd reactionsofaminoacetalswithcnucleophilesasanewmethodforthesynthesisofdihetarylmethanederivativeswithataurinefragment
AT gazizovas reactionsofaminoacetalswithcnucleophilesasanewmethodforthesynthesisofdihetarylmethanederivativeswithataurinefragment
AT burilovar reactionsofaminoacetalswithcnucleophilesasanewmethodforthesynthesisofdihetarylmethanederivativeswithataurinefragment
AT pudovikma reactionsofaminoacetalswithcnucleophilesasanewmethodforthesynthesisofdihetarylmethanederivativeswithataurinefragment

Ejemplares similares