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Synthesis of spiro[4.4]thiadiazole derivatives via double 1,3-dipolar cycloaddition of hydrazonyl chlorides with carbon disulfide
An operationally simple and convenient synthesis method toward a series of diverse spiro[4.4]thiadiazole derivatives via double [3 + 2] 1,3-dipolar cycloaddition of nitrilimines generated in situ from hydrazonyl chlorides with carbon disulfide has been achieved under mild reaction conditions.
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033500/ https://www.ncbi.nlm.nih.gov/pubmed/35480901 http://dx.doi.org/10.1039/d1ra03229a |
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author | Wang, Kai-Kai Li, Yan-Li Guo, Dong-Guang Pan, Peng-Tao Sun, Aili Chen, Rongxiang |
author_facet | Wang, Kai-Kai Li, Yan-Li Guo, Dong-Guang Pan, Peng-Tao Sun, Aili Chen, Rongxiang |
author_sort | Wang, Kai-Kai |
collection | PubMed |
description | An operationally simple and convenient synthesis method toward a series of diverse spiro[4.4]thiadiazole derivatives via double [3 + 2] 1,3-dipolar cycloaddition of nitrilimines generated in situ from hydrazonyl chlorides with carbon disulfide has been achieved under mild reaction conditions. |
format | Online Article Text |
id | pubmed-9033500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90335002022-04-26 Synthesis of spiro[4.4]thiadiazole derivatives via double 1,3-dipolar cycloaddition of hydrazonyl chlorides with carbon disulfide Wang, Kai-Kai Li, Yan-Li Guo, Dong-Guang Pan, Peng-Tao Sun, Aili Chen, Rongxiang RSC Adv Chemistry An operationally simple and convenient synthesis method toward a series of diverse spiro[4.4]thiadiazole derivatives via double [3 + 2] 1,3-dipolar cycloaddition of nitrilimines generated in situ from hydrazonyl chlorides with carbon disulfide has been achieved under mild reaction conditions. The Royal Society of Chemistry 2021-05-21 /pmc/articles/PMC9033500/ /pubmed/35480901 http://dx.doi.org/10.1039/d1ra03229a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Wang, Kai-Kai Li, Yan-Li Guo, Dong-Guang Pan, Peng-Tao Sun, Aili Chen, Rongxiang Synthesis of spiro[4.4]thiadiazole derivatives via double 1,3-dipolar cycloaddition of hydrazonyl chlorides with carbon disulfide |
title | Synthesis of spiro[4.4]thiadiazole derivatives via double 1,3-dipolar cycloaddition of hydrazonyl chlorides with carbon disulfide |
title_full | Synthesis of spiro[4.4]thiadiazole derivatives via double 1,3-dipolar cycloaddition of hydrazonyl chlorides with carbon disulfide |
title_fullStr | Synthesis of spiro[4.4]thiadiazole derivatives via double 1,3-dipolar cycloaddition of hydrazonyl chlorides with carbon disulfide |
title_full_unstemmed | Synthesis of spiro[4.4]thiadiazole derivatives via double 1,3-dipolar cycloaddition of hydrazonyl chlorides with carbon disulfide |
title_short | Synthesis of spiro[4.4]thiadiazole derivatives via double 1,3-dipolar cycloaddition of hydrazonyl chlorides with carbon disulfide |
title_sort | synthesis of spiro[4.4]thiadiazole derivatives via double 1,3-dipolar cycloaddition of hydrazonyl chlorides with carbon disulfide |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033500/ https://www.ncbi.nlm.nih.gov/pubmed/35480901 http://dx.doi.org/10.1039/d1ra03229a |
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