Cargando…
Formal Enone α-Arylation via I(III)-Mediated Aryl Migration/Elimination
[Image: see text] A formal enone α-arylation is described. This metal-free transformation relies on the I(III)-mediated skeletal reorganization of silyl enol ethers and features mild conditions, good yields, and high stereoselectivities for β-substituted enones.
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2021
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985840/ https://www.ncbi.nlm.nih.gov/pubmed/33635665 http://dx.doi.org/10.1021/acs.orglett.1c00251 |
_version_ | 1783668329042411520 |
---|---|
author | Martins, Bruna S. Kaiser, Daniel Bauer, Adriano Tiefenbrunner, Irmgard Maulide, Nuno |
author_facet | Martins, Bruna S. Kaiser, Daniel Bauer, Adriano Tiefenbrunner, Irmgard Maulide, Nuno |
author_sort | Martins, Bruna S. |
collection | PubMed |
description | [Image: see text] A formal enone α-arylation is described. This metal-free transformation relies on the I(III)-mediated skeletal reorganization of silyl enol ethers and features mild conditions, good yields, and high stereoselectivities for β-substituted enones. |
format | Online Article Text |
id | pubmed-7985840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-79858402021-03-23 Formal Enone α-Arylation via I(III)-Mediated Aryl Migration/Elimination Martins, Bruna S. Kaiser, Daniel Bauer, Adriano Tiefenbrunner, Irmgard Maulide, Nuno Org Lett [Image: see text] A formal enone α-arylation is described. This metal-free transformation relies on the I(III)-mediated skeletal reorganization of silyl enol ethers and features mild conditions, good yields, and high stereoselectivities for β-substituted enones. American Chemical Society 2021-02-26 2021-03-19 /pmc/articles/PMC7985840/ /pubmed/33635665 http://dx.doi.org/10.1021/acs.orglett.1c00251 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Martins, Bruna S. Kaiser, Daniel Bauer, Adriano Tiefenbrunner, Irmgard Maulide, Nuno Formal Enone α-Arylation via I(III)-Mediated Aryl Migration/Elimination |
title | Formal Enone α-Arylation via I(III)-Mediated
Aryl Migration/Elimination |
title_full | Formal Enone α-Arylation via I(III)-Mediated
Aryl Migration/Elimination |
title_fullStr | Formal Enone α-Arylation via I(III)-Mediated
Aryl Migration/Elimination |
title_full_unstemmed | Formal Enone α-Arylation via I(III)-Mediated
Aryl Migration/Elimination |
title_short | Formal Enone α-Arylation via I(III)-Mediated
Aryl Migration/Elimination |
title_sort | formal enone α-arylation via i(iii)-mediated
aryl migration/elimination |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985840/ https://www.ncbi.nlm.nih.gov/pubmed/33635665 http://dx.doi.org/10.1021/acs.orglett.1c00251 |
work_keys_str_mv | AT martinsbrunas formalenoneaarylationviaiiiimediatedarylmigrationelimination AT kaiserdaniel formalenoneaarylationviaiiiimediatedarylmigrationelimination AT baueradriano formalenoneaarylationviaiiiimediatedarylmigrationelimination AT tiefenbrunnerirmgard formalenoneaarylationviaiiiimediatedarylmigrationelimination AT maulidenuno formalenoneaarylationviaiiiimediatedarylmigrationelimination |