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An Efficient Method for Selective Syntheses of Sodium Selenide and Dialkyl Selenides

The studies on the selective synthesis of dialkyl selenide compounds 1 were presented. Overcoming the complexity and difficulty of selenides (R-Se-R) and/or multiselenides (R-Se(n)-R; n ≥ 2), we aimed to optimize the reaction condition for the tolerable preparation of sodium selenide (Na(2)Se) by re...

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Autores principales: Shin, Na Hye, Lim, Yoo Jin, Kim, Chorong, Kim, Ye Eun, Jeong, Yu Ra, Cho, Hyunsung, Park, Myung-Sook, Lee, Sang Hyup
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414418/
https://www.ncbi.nlm.nih.gov/pubmed/36014475
http://dx.doi.org/10.3390/molecules27165224
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author Shin, Na Hye
Lim, Yoo Jin
Kim, Chorong
Kim, Ye Eun
Jeong, Yu Ra
Cho, Hyunsung
Park, Myung-Sook
Lee, Sang Hyup
author_facet Shin, Na Hye
Lim, Yoo Jin
Kim, Chorong
Kim, Ye Eun
Jeong, Yu Ra
Cho, Hyunsung
Park, Myung-Sook
Lee, Sang Hyup
author_sort Shin, Na Hye
collection PubMed
description The studies on the selective synthesis of dialkyl selenide compounds 1 were presented. Overcoming the complexity and difficulty of selenides (R-Se-R) and/or multiselenides (R-Se(n)-R; n ≥ 2), we aimed to optimize the reaction condition for the tolerable preparation of sodium selenide (Na(2)Se) by reducing Se with NaBH(4), and then to achieve selective syntheses of dialkyl selenides 1 by subsequently treating the obtained sodium selenide with alkyl halides (RX). Consequently, various dialkyl selenides 1 were efficiently synthesized in good-to-moderate yields. The investigations on reaction pathways and solvent studies were also described.
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spelling pubmed-94144182022-08-27 An Efficient Method for Selective Syntheses of Sodium Selenide and Dialkyl Selenides Shin, Na Hye Lim, Yoo Jin Kim, Chorong Kim, Ye Eun Jeong, Yu Ra Cho, Hyunsung Park, Myung-Sook Lee, Sang Hyup Molecules Article The studies on the selective synthesis of dialkyl selenide compounds 1 were presented. Overcoming the complexity and difficulty of selenides (R-Se-R) and/or multiselenides (R-Se(n)-R; n ≥ 2), we aimed to optimize the reaction condition for the tolerable preparation of sodium selenide (Na(2)Se) by reducing Se with NaBH(4), and then to achieve selective syntheses of dialkyl selenides 1 by subsequently treating the obtained sodium selenide with alkyl halides (RX). Consequently, various dialkyl selenides 1 were efficiently synthesized in good-to-moderate yields. The investigations on reaction pathways and solvent studies were also described. MDPI 2022-08-16 /pmc/articles/PMC9414418/ /pubmed/36014475 http://dx.doi.org/10.3390/molecules27165224 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shin, Na Hye
Lim, Yoo Jin
Kim, Chorong
Kim, Ye Eun
Jeong, Yu Ra
Cho, Hyunsung
Park, Myung-Sook
Lee, Sang Hyup
An Efficient Method for Selective Syntheses of Sodium Selenide and Dialkyl Selenides
title An Efficient Method for Selective Syntheses of Sodium Selenide and Dialkyl Selenides
title_full An Efficient Method for Selective Syntheses of Sodium Selenide and Dialkyl Selenides
title_fullStr An Efficient Method for Selective Syntheses of Sodium Selenide and Dialkyl Selenides
title_full_unstemmed An Efficient Method for Selective Syntheses of Sodium Selenide and Dialkyl Selenides
title_short An Efficient Method for Selective Syntheses of Sodium Selenide and Dialkyl Selenides
title_sort efficient method for selective syntheses of sodium selenide and dialkyl selenides
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414418/
https://www.ncbi.nlm.nih.gov/pubmed/36014475
http://dx.doi.org/10.3390/molecules27165224
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