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Indium-Catalyzed Direct Conversion of Lactones into Thiolactones Using a Disilathiane as a Sulfur Source
An indium-catalyzed reaction of lactones and a disilathiane leading to thiolactones is described. The direct synthesis of thiolactones from lactones with an appropriate sulfur source is one of the most attractive approaches in organic and pharmaceutical chemistry. In this context, we found an indium...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100358/ https://www.ncbi.nlm.nih.gov/pubmed/29865263 http://dx.doi.org/10.3390/molecules23061339 |
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author | Ogiwara, Yohei Takano, Ken Horikawa, Shuhei Sakai, Norio |
author_facet | Ogiwara, Yohei Takano, Ken Horikawa, Shuhei Sakai, Norio |
author_sort | Ogiwara, Yohei |
collection | PubMed |
description | An indium-catalyzed reaction of lactones and a disilathiane leading to thiolactones is described. The direct synthesis of thiolactones from lactones with an appropriate sulfur source is one of the most attractive approaches in organic and pharmaceutical chemistry. In this context, we found an indium-catalyzed direct conversion of lactones into thiolactones in the presence of elemental sulfur and a hydrosilane via formation of the disilathiane in situ. On the basis of the previous reaction, the application utilizing the disilathiane as a sulfur source was performed herein for the efficient synthesis of a variety of thiolactone derivatives from lactones by an indium catalyst. |
format | Online Article Text |
id | pubmed-6100358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61003582018-11-13 Indium-Catalyzed Direct Conversion of Lactones into Thiolactones Using a Disilathiane as a Sulfur Source Ogiwara, Yohei Takano, Ken Horikawa, Shuhei Sakai, Norio Molecules Article An indium-catalyzed reaction of lactones and a disilathiane leading to thiolactones is described. The direct synthesis of thiolactones from lactones with an appropriate sulfur source is one of the most attractive approaches in organic and pharmaceutical chemistry. In this context, we found an indium-catalyzed direct conversion of lactones into thiolactones in the presence of elemental sulfur and a hydrosilane via formation of the disilathiane in situ. On the basis of the previous reaction, the application utilizing the disilathiane as a sulfur source was performed herein for the efficient synthesis of a variety of thiolactone derivatives from lactones by an indium catalyst. MDPI 2018-06-02 /pmc/articles/PMC6100358/ /pubmed/29865263 http://dx.doi.org/10.3390/molecules23061339 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ogiwara, Yohei Takano, Ken Horikawa, Shuhei Sakai, Norio Indium-Catalyzed Direct Conversion of Lactones into Thiolactones Using a Disilathiane as a Sulfur Source |
title | Indium-Catalyzed Direct Conversion of Lactones into Thiolactones Using a Disilathiane as a Sulfur Source |
title_full | Indium-Catalyzed Direct Conversion of Lactones into Thiolactones Using a Disilathiane as a Sulfur Source |
title_fullStr | Indium-Catalyzed Direct Conversion of Lactones into Thiolactones Using a Disilathiane as a Sulfur Source |
title_full_unstemmed | Indium-Catalyzed Direct Conversion of Lactones into Thiolactones Using a Disilathiane as a Sulfur Source |
title_short | Indium-Catalyzed Direct Conversion of Lactones into Thiolactones Using a Disilathiane as a Sulfur Source |
title_sort | indium-catalyzed direct conversion of lactones into thiolactones using a disilathiane as a sulfur source |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100358/ https://www.ncbi.nlm.nih.gov/pubmed/29865263 http://dx.doi.org/10.3390/molecules23061339 |
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