Passerini-type reaction of boronic acids enables α-hydroxyketones synthesis
Multicomponent reactions enable the rapid construction of diverse molecular scaffolds with modularity and step economy. In this work, the authors report the use of boronic acids as carbon nucleophiles in a Passerini-type three-component coupling reaction towards an expanded inventory of α-hydroxyket...
Guardado en:
Autores principales: | , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/633cce68c78741b99add99a0e30b21be |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:633cce68c78741b99add99a0e30b21be |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:633cce68c78741b99add99a0e30b21be2021-12-02T14:19:04ZPasserini-type reaction of boronic acids enables α-hydroxyketones synthesis10.1038/s41467-020-20727-72041-1723https://doaj.org/article/633cce68c78741b99add99a0e30b21be2021-01-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-20727-7https://doaj.org/toc/2041-1723Multicomponent reactions enable the rapid construction of diverse molecular scaffolds with modularity and step economy. In this work, the authors report the use of boronic acids as carbon nucleophiles in a Passerini-type three-component coupling reaction towards an expanded inventory of α-hydroxyketones.Kai YangFeng ZhangTongchang FangChaokun LiWangyang LiQiuling SongNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-9 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Science Q |
spellingShingle |
Science Q Kai Yang Feng Zhang Tongchang Fang Chaokun Li Wangyang Li Qiuling Song Passerini-type reaction of boronic acids enables α-hydroxyketones synthesis |
description |
Multicomponent reactions enable the rapid construction of diverse molecular scaffolds with modularity and step economy. In this work, the authors report the use of boronic acids as carbon nucleophiles in a Passerini-type three-component coupling reaction towards an expanded inventory of α-hydroxyketones. |
format |
article |
author |
Kai Yang Feng Zhang Tongchang Fang Chaokun Li Wangyang Li Qiuling Song |
author_facet |
Kai Yang Feng Zhang Tongchang Fang Chaokun Li Wangyang Li Qiuling Song |
author_sort |
Kai Yang |
title |
Passerini-type reaction of boronic acids enables α-hydroxyketones synthesis |
title_short |
Passerini-type reaction of boronic acids enables α-hydroxyketones synthesis |
title_full |
Passerini-type reaction of boronic acids enables α-hydroxyketones synthesis |
title_fullStr |
Passerini-type reaction of boronic acids enables α-hydroxyketones synthesis |
title_full_unstemmed |
Passerini-type reaction of boronic acids enables α-hydroxyketones synthesis |
title_sort |
passerini-type reaction of boronic acids enables α-hydroxyketones synthesis |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/633cce68c78741b99add99a0e30b21be |
work_keys_str_mv |
AT kaiyang passerinitypereactionofboronicacidsenablesahydroxyketonessynthesis AT fengzhang passerinitypereactionofboronicacidsenablesahydroxyketonessynthesis AT tongchangfang passerinitypereactionofboronicacidsenablesahydroxyketonessynthesis AT chaokunli passerinitypereactionofboronicacidsenablesahydroxyketonessynthesis AT wangyangli passerinitypereactionofboronicacidsenablesahydroxyketonessynthesis AT qiulingsong passerinitypereactionofboronicacidsenablesahydroxyketonessynthesis |
_version_ |
1718391609736822784 |