Difluorocarbene enables to access 2-fluoroindoles from ortho-vinylanilines

2-Fluoroindoles are an important structural scaffold in many bioactive or therapeutic agents, but efficient constructions of 2-fluoroindole derivatives are very sparce. Here the authors report an efficient and general strategy for the construction of 2-fluoroindoles in which a wide variety of 2-fluo...

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Main Authors: Jianke Su, Xinyuan Hu, Hua Huang, Yu Guo, Qiuling Song
Format: Article
Language:English
Published: Nature Portfolio 2021-08-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-021-25313-z
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author Jianke Su
Xinyuan Hu
Hua Huang
Yu Guo
Qiuling Song
author_facet Jianke Su
Xinyuan Hu
Hua Huang
Yu Guo
Qiuling Song
author_sort Jianke Su
collection DOAJ
description 2-Fluoroindoles are an important structural scaffold in many bioactive or therapeutic agents, but efficient constructions of 2-fluoroindole derivatives are very sparce. Here the authors report an efficient and general strategy for the construction of 2-fluoroindoles in which a wide variety of 2-fluoroindoles were accessed with high efficiency and chemoselectivity.
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spelling doaj.art-b4f06b0e23554d8d98d302d48e9c40542022-12-21T22:59:56ZengNature PortfolioNature Communications2041-17232021-08-0112111010.1038/s41467-021-25313-zDifluorocarbene enables to access 2-fluoroindoles from ortho-vinylanilinesJianke Su0Xinyuan Hu1Hua Huang2Yu Guo3Qiuling Song4Institute of Next Generation Matter Transformation, College of Material Sciences Engineering, Huaqiao UniversityInstitute of Next Generation Matter Transformation, College of Material Sciences Engineering, Huaqiao UniversityInstitute of Next Generation Matter Transformation, College of Material Sciences Engineering, Huaqiao UniversityInstitute of Next Generation Matter Transformation, College of Material Sciences Engineering, Huaqiao UniversityInstitute of Next Generation Matter Transformation, College of Material Sciences Engineering, Huaqiao University2-Fluoroindoles are an important structural scaffold in many bioactive or therapeutic agents, but efficient constructions of 2-fluoroindole derivatives are very sparce. Here the authors report an efficient and general strategy for the construction of 2-fluoroindoles in which a wide variety of 2-fluoroindoles were accessed with high efficiency and chemoselectivity.https://doi.org/10.1038/s41467-021-25313-z
spellingShingle Jianke Su
Xinyuan Hu
Hua Huang
Yu Guo
Qiuling Song
Difluorocarbene enables to access 2-fluoroindoles from ortho-vinylanilines
Nature Communications
title Difluorocarbene enables to access 2-fluoroindoles from ortho-vinylanilines
title_full Difluorocarbene enables to access 2-fluoroindoles from ortho-vinylanilines
title_fullStr Difluorocarbene enables to access 2-fluoroindoles from ortho-vinylanilines
title_full_unstemmed Difluorocarbene enables to access 2-fluoroindoles from ortho-vinylanilines
title_short Difluorocarbene enables to access 2-fluoroindoles from ortho-vinylanilines
title_sort difluorocarbene enables to access 2 fluoroindoles from ortho vinylanilines
url https://doi.org/10.1038/s41467-021-25313-z
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AT xinyuanhu difluorocarbeneenablestoaccess2fluoroindolesfromorthovinylanilines
AT huahuang difluorocarbeneenablestoaccess2fluoroindolesfromorthovinylanilines
AT yuguo difluorocarbeneenablestoaccess2fluoroindolesfromorthovinylanilines
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