Triflic Acid-Catalyzed Chemo- and Site-Selective C−H Bond Functionalization of Phenols With 1,3-Dienes

Zhenli Liu; Guanghui Li; Tengfei Yao; Junliang Zhang; Lu Liu

doi:10.1002/adsc.202100181

Triflic Acid-Catalyzed Chemo- and Site-Selective C−H Bond Functionalization of Phenols With 1,3-Dienes

Zhenli Liu, Guanghui Li, Tengfei Yao, Junliang Zhang^*, Lu Liu^*

^*Corresponding author for this work

School of Chemistry and Molecular Engineering

Research output: Contribution to journal › Article › peer-review

14 Scopus citations

Abstract

Herein, a Brønsted acid-catalyzed C(sp²)−H functionalization of free phenols with 1,3-dienes has been developed. In this transformation, triflic acid promoted C−H bond functionalization under mild conditions in a site-selective manner. (Figure presented.).

Original language	English
Pages (from-to)	2740-2745
Number of pages	6
Journal	Advanced Synthesis and Catalysis
Volume	363
Issue number	11
DOIs	https://doi.org/10.1002/adsc.202100181
State	Published - 8 Jun 2021

Keywords

1,3-diene
Allylic alkylation
C−H bond functionalization
Phenols
Site-selective

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10.1002/adsc.202100181

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title = "Triflic Acid-Catalyzed Chemo- and Site-Selective C−H Bond Functionalization of Phenols With 1,3-Dienes",

abstract = "Herein, a Br{\o}nsted acid-catalyzed C(sp2)−H functionalization of free phenols with 1,3-dienes has been developed. In this transformation, triflic acid promoted C−H bond functionalization under mild conditions in a site-selective manner. (Figure presented.).",

keywords = "1,3-diene, Allylic alkylation, C−H bond functionalization, Phenols, Site-selective",

author = "Zhenli Liu and Guanghui Li and Tengfei Yao and Junliang Zhang and Lu Liu",

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T1 - Triflic Acid-Catalyzed Chemo- and Site-Selective C−H Bond Functionalization of Phenols With 1,3-Dienes

AU - Liu, Zhenli

AU - Li, Guanghui

AU - Yao, Tengfei

AU - Zhang, Junliang

AU - Liu, Lu

PY - 2021/6/8

Y1 - 2021/6/8

N2 - Herein, a Brønsted acid-catalyzed C(sp2)−H functionalization of free phenols with 1,3-dienes has been developed. In this transformation, triflic acid promoted C−H bond functionalization under mild conditions in a site-selective manner. (Figure presented.).

AB - Herein, a Brønsted acid-catalyzed C(sp2)−H functionalization of free phenols with 1,3-dienes has been developed. In this transformation, triflic acid promoted C−H bond functionalization under mild conditions in a site-selective manner. (Figure presented.).

KW - 1,3-diene

KW - Allylic alkylation

KW - C−H bond functionalization

KW - Phenols

KW - Site-selective

UR - https://www.scopus.com/pages/publications/85103417643

U2 - 10.1002/adsc.202100181

DO - 10.1002/adsc.202100181

M3 - 文章

AN - SCOPUS:85103417643

SN - 1615-4150

VL - 363

SP - 2740

EP - 2745

JO - Advanced Synthesis and Catalysis

JF - Advanced Synthesis and Catalysis

IS - 11

ER -

Triflic Acid-Catalyzed Chemo- and Site-Selective C−H Bond Functionalization of Phenols With 1,3-Dienes

Abstract

Keywords

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