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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...

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Autores principales: Męcik, Patrycja, Pigulski, Bartłomiej, Szafert, Sławomir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
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.
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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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