Asymmetric C(sp3)–H functionalization of unactivated alkylarenes such as toluene enabled by chiral Brønsted base catalysts
Benzylic functionalisation of unactivated toluenes remains a challenge in asymmetric catalysis. Here a chiral Brønsted base catalyses the enantioselective C(sp3)-H functionalization of unactivated alkylarenes, enabling carbon-carbon bond formation at benzylic positions of toluene derivatives.
Guardado en:
Autores principales: | , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/9539fd65b1104cd5b231246152e7078f |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:9539fd65b1104cd5b231246152e7078f |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:9539fd65b1104cd5b231246152e7078f2021-12-02T16:30:39ZAsymmetric C(sp3)–H functionalization of unactivated alkylarenes such as toluene enabled by chiral Brønsted base catalysts10.1038/s42004-021-00459-52399-3669https://doaj.org/article/9539fd65b1104cd5b231246152e7078f2021-03-01T00:00:00Zhttps://doi.org/10.1038/s42004-021-00459-5https://doaj.org/toc/2399-3669Benzylic functionalisation of unactivated toluenes remains a challenge in asymmetric catalysis. Here a chiral Brønsted base catalyses the enantioselective C(sp3)-H functionalization of unactivated alkylarenes, enabling carbon-carbon bond formation at benzylic positions of toluene derivatives.Tsubasa HirataIo SatoYasuhiro YamashitaShū KobayashiNature PortfolioarticleChemistryQD1-999ENCommunications Chemistry, Vol 4, Iss 1, Pp 1-8 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Chemistry QD1-999 |
spellingShingle |
Chemistry QD1-999 Tsubasa Hirata Io Sato Yasuhiro Yamashita Shū Kobayashi Asymmetric C(sp3)–H functionalization of unactivated alkylarenes such as toluene enabled by chiral Brønsted base catalysts |
description |
Benzylic functionalisation of unactivated toluenes remains a challenge in asymmetric catalysis. Here a chiral Brønsted base catalyses the enantioselective C(sp3)-H functionalization of unactivated alkylarenes, enabling carbon-carbon bond formation at benzylic positions of toluene derivatives. |
format |
article |
author |
Tsubasa Hirata Io Sato Yasuhiro Yamashita Shū Kobayashi |
author_facet |
Tsubasa Hirata Io Sato Yasuhiro Yamashita Shū Kobayashi |
author_sort |
Tsubasa Hirata |
title |
Asymmetric C(sp3)–H functionalization of unactivated alkylarenes such as toluene enabled by chiral Brønsted base catalysts |
title_short |
Asymmetric C(sp3)–H functionalization of unactivated alkylarenes such as toluene enabled by chiral Brønsted base catalysts |
title_full |
Asymmetric C(sp3)–H functionalization of unactivated alkylarenes such as toluene enabled by chiral Brønsted base catalysts |
title_fullStr |
Asymmetric C(sp3)–H functionalization of unactivated alkylarenes such as toluene enabled by chiral Brønsted base catalysts |
title_full_unstemmed |
Asymmetric C(sp3)–H functionalization of unactivated alkylarenes such as toluene enabled by chiral Brønsted base catalysts |
title_sort |
asymmetric c(sp3)–h functionalization of unactivated alkylarenes such as toluene enabled by chiral brønsted base catalysts |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/9539fd65b1104cd5b231246152e7078f |
work_keys_str_mv |
AT tsubasahirata asymmetriccsp3hfunctionalizationofunactivatedalkylarenessuchastolueneenabledbychiralbrønstedbasecatalysts AT iosato asymmetriccsp3hfunctionalizationofunactivatedalkylarenessuchastolueneenabledbychiralbrønstedbasecatalysts AT yasuhiroyamashita asymmetriccsp3hfunctionalizationofunactivatedalkylarenessuchastolueneenabledbychiralbrønstedbasecatalysts AT shukobayashi asymmetriccsp3hfunctionalizationofunactivatedalkylarenessuchastolueneenabledbychiralbrønstedbasecatalysts |
_version_ |
1718383942372950016 |