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N-Substituted S-Alkyl Carbamothioates in the Synthesis of Nitrogen-containing Functional Derivatives of the Adamantane Series
A series of new asymmetric ureas, urethanes, and other derivatives of the framework structure have been synthesized by the reactions of adamantan-1-yl isocyanate generated in situ by the thermolysis of carbamothioates with nitrogen-containing nucleophiles and alcohols.
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pleiades Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473989/ http://dx.doi.org/10.1134/S1070428021080078 |
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author | Klimochkin, Yu. N. Ivleva, E. A. |
author_facet | Klimochkin, Yu. N. Ivleva, E. A. |
author_sort | Klimochkin, Yu. N. |
collection | PubMed |
description | A series of new asymmetric ureas, urethanes, and other derivatives of the framework structure have been synthesized by the reactions of adamantan-1-yl isocyanate generated in situ by the thermolysis of carbamothioates with nitrogen-containing nucleophiles and alcohols. |
format | Online Article Text |
id | pubmed-8473989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Pleiades Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-84739892021-09-27 N-Substituted S-Alkyl Carbamothioates in the Synthesis of Nitrogen-containing Functional Derivatives of the Adamantane Series Klimochkin, Yu. N. Ivleva, E. A. Russ J Org Chem Article A series of new asymmetric ureas, urethanes, and other derivatives of the framework structure have been synthesized by the reactions of adamantan-1-yl isocyanate generated in situ by the thermolysis of carbamothioates with nitrogen-containing nucleophiles and alcohols. Pleiades Publishing 2021-09-27 2021 /pmc/articles/PMC8473989/ http://dx.doi.org/10.1134/S1070428021080078 Text en © Pleiades Publishing, Ltd. 2021 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 Klimochkin, Yu. N. Ivleva, E. A. N-Substituted S-Alkyl Carbamothioates in the Synthesis of Nitrogen-containing Functional Derivatives of the Adamantane Series |
title | N-Substituted S-Alkyl Carbamothioates in the Synthesis of Nitrogen-containing Functional Derivatives of the Adamantane Series |
title_full | N-Substituted S-Alkyl Carbamothioates in the Synthesis of Nitrogen-containing Functional Derivatives of the Adamantane Series |
title_fullStr | N-Substituted S-Alkyl Carbamothioates in the Synthesis of Nitrogen-containing Functional Derivatives of the Adamantane Series |
title_full_unstemmed | N-Substituted S-Alkyl Carbamothioates in the Synthesis of Nitrogen-containing Functional Derivatives of the Adamantane Series |
title_short | N-Substituted S-Alkyl Carbamothioates in the Synthesis of Nitrogen-containing Functional Derivatives of the Adamantane Series |
title_sort | n-substituted s-alkyl carbamothioates in the synthesis of nitrogen-containing functional derivatives of the adamantane series |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473989/ http://dx.doi.org/10.1134/S1070428021080078 |
work_keys_str_mv | AT klimochkinyun nsubstitutedsalkylcarbamothioatesinthesynthesisofnitrogencontainingfunctionalderivativesoftheadamantaneseries AT ivlevaea nsubstitutedsalkylcarbamothioatesinthesynthesisofnitrogencontainingfunctionalderivativesoftheadamantaneseries |