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When SF(5) outplays CF(3): effects of pentafluorosulfanyl decorated scorpionates on copper
Polyfluorinated, electron-withdrawing, and sterically demanding supporting ligands are of significant value in chemistry. Here we report the assembly and use of a bis(pyrazolyl)borate, [Ph(2)B(3-(SF(5))Pz)(2)](−) that combines all such features, and involves underutilized pentafluorosulfanyl substit...
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/PMC8580053/ https://www.ncbi.nlm.nih.gov/pubmed/34881014 http://dx.doi.org/10.1039/d1sc04846e |
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author | Noonikara-Poyil, Anurag Muñoz-Castro, Alvaro Boretskyi, Andrii Mykhailiuk, Pavel K. Dias, H. V. Rasika |
author_facet | Noonikara-Poyil, Anurag Muñoz-Castro, Alvaro Boretskyi, Andrii Mykhailiuk, Pavel K. Dias, H. V. Rasika |
author_sort | Noonikara-Poyil, Anurag |
collection | PubMed |
description | Polyfluorinated, electron-withdrawing, and sterically demanding supporting ligands are of significant value in chemistry. Here we report the assembly and use of a bis(pyrazolyl)borate, [Ph(2)B(3-(SF(5))Pz)(2)](−) that combines all such features, and involves underutilized pentafluorosulfanyl substituents. The ethylene and carbonyl chemistry of copper(i) supported by [Ph(2)B(3-(SF(5))Pz)(2)](−), a comparison to the trifluoromethylated counterparts involving [Ph(2)B(3-(CF(3))Pz)(2)](−), as well as copper catalyzed cyclopropanation of styrene with ethyl diazoacetate and CF(3)CHN(2) are presented. The results from cyclopropanation show that SF(5) groups dramatically improved the yields and stereoselectivity compared to the CF(3). |
format | Online Article Text |
id | pubmed-8580053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-85800532021-12-07 When SF(5) outplays CF(3): effects of pentafluorosulfanyl decorated scorpionates on copper Noonikara-Poyil, Anurag Muñoz-Castro, Alvaro Boretskyi, Andrii Mykhailiuk, Pavel K. Dias, H. V. Rasika Chem Sci Chemistry Polyfluorinated, electron-withdrawing, and sterically demanding supporting ligands are of significant value in chemistry. Here we report the assembly and use of a bis(pyrazolyl)borate, [Ph(2)B(3-(SF(5))Pz)(2)](−) that combines all such features, and involves underutilized pentafluorosulfanyl substituents. The ethylene and carbonyl chemistry of copper(i) supported by [Ph(2)B(3-(SF(5))Pz)(2)](−), a comparison to the trifluoromethylated counterparts involving [Ph(2)B(3-(CF(3))Pz)(2)](−), as well as copper catalyzed cyclopropanation of styrene with ethyl diazoacetate and CF(3)CHN(2) are presented. The results from cyclopropanation show that SF(5) groups dramatically improved the yields and stereoselectivity compared to the CF(3). The Royal Society of Chemistry 2021-10-15 /pmc/articles/PMC8580053/ /pubmed/34881014 http://dx.doi.org/10.1039/d1sc04846e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Noonikara-Poyil, Anurag Muñoz-Castro, Alvaro Boretskyi, Andrii Mykhailiuk, Pavel K. Dias, H. V. Rasika When SF(5) outplays CF(3): effects of pentafluorosulfanyl decorated scorpionates on copper |
title | When SF(5) outplays CF(3): effects of pentafluorosulfanyl decorated scorpionates on copper |
title_full | When SF(5) outplays CF(3): effects of pentafluorosulfanyl decorated scorpionates on copper |
title_fullStr | When SF(5) outplays CF(3): effects of pentafluorosulfanyl decorated scorpionates on copper |
title_full_unstemmed | When SF(5) outplays CF(3): effects of pentafluorosulfanyl decorated scorpionates on copper |
title_short | When SF(5) outplays CF(3): effects of pentafluorosulfanyl decorated scorpionates on copper |
title_sort | when sf(5) outplays cf(3): effects of pentafluorosulfanyl decorated scorpionates on copper |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580053/ https://www.ncbi.nlm.nih.gov/pubmed/34881014 http://dx.doi.org/10.1039/d1sc04846e |
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