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Serendipitous Formation of Various Selenium Heterocycles Hidden in the Classical Synthesis of Selenophene
[Image: see text] Synthesis of complex di(selenophen-3-yl)diselenides and 3-methylene-3H-1,2-diselenoles directly from 1-bromobutadiynes is described. The transformation is performed under conditions used before for the synthesis of simple selenophenes from butadiynes. The reaction is operationally...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874900/ https://www.ncbi.nlm.nih.gov/pubmed/33502204 http://dx.doi.org/10.1021/acs.orglett.0c04275 |
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author | Męcik, Patrycja Pigulski, Bartłomiej Szafert, Sławomir |
author_facet | Męcik, Patrycja Pigulski, Bartłomiej Szafert, Sławomir |
author_sort | Męcik, Patrycja |
collection | PubMed |
description | [Image: see text] Synthesis of complex di(selenophen-3-yl)diselenides and 3-methylene-3H-1,2-diselenoles directly from 1-bromobutadiynes is described. The transformation is performed under conditions used before for the synthesis of simple selenophenes from butadiynes. The reaction is operationally straightforward, and complex products were obtained in high yields. Structures of the final products were unambiguously confirmed by the means of (77)Se NMR and single-crystal X-ray diffraction. |
format | Online Article Text |
id | pubmed-7874900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-78749002021-02-11 Serendipitous Formation of Various Selenium Heterocycles Hidden in the Classical Synthesis of Selenophene Męcik, Patrycja Pigulski, Bartłomiej Szafert, Sławomir Org Lett [Image: see text] Synthesis of complex di(selenophen-3-yl)diselenides and 3-methylene-3H-1,2-diselenoles directly from 1-bromobutadiynes is described. The transformation is performed under conditions used before for the synthesis of simple selenophenes from butadiynes. The reaction is operationally straightforward, and complex products were obtained in high yields. Structures of the final products were unambiguously confirmed by the means of (77)Se NMR and single-crystal X-ray diffraction. American Chemical Society 2021-01-27 2021-02-05 /pmc/articles/PMC7874900/ /pubmed/33502204 http://dx.doi.org/10.1021/acs.orglett.0c04275 Text en © 2021 The Authors. Published by American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Męcik, Patrycja Pigulski, Bartłomiej Szafert, Sławomir Serendipitous Formation of Various Selenium Heterocycles Hidden in the Classical Synthesis of Selenophene |
title | Serendipitous Formation of Various Selenium Heterocycles
Hidden in the Classical Synthesis of Selenophene |
title_full | Serendipitous Formation of Various Selenium Heterocycles
Hidden in the Classical Synthesis of Selenophene |
title_fullStr | Serendipitous Formation of Various Selenium Heterocycles
Hidden in the Classical Synthesis of Selenophene |
title_full_unstemmed | Serendipitous Formation of Various Selenium Heterocycles
Hidden in the Classical Synthesis of Selenophene |
title_short | Serendipitous Formation of Various Selenium Heterocycles
Hidden in the Classical Synthesis of Selenophene |
title_sort | serendipitous formation of various selenium heterocycles
hidden in the classical synthesis of selenophene |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874900/ https://www.ncbi.nlm.nih.gov/pubmed/33502204 http://dx.doi.org/10.1021/acs.orglett.0c04275 |
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