Aqueous C-H aminomethylation of phenols by iodine catalysis

Zhi Hua Zhou; Ben Wang; Yao Ding; Teck Peng Loh; Jie Sheng Tian

doi:10.1039/d2cc05746h

Aqueous C-H aminomethylation of phenols by iodine catalysis

Zhi Hua Zhou, Ben Wang, Yao Ding, Teck Peng Loh, Jie Sheng Tian

School of Chemistry and Moleculai Engineering

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

5 Scopus citations

Abstract

A transition-metal-free strategy regarding an iodine-sodium percarbonate catalysis to achieve the ortho-aminomethylation of phenols in aqueous media has been developed. This method can effectively broaden a wide range of phenols, tolerate sensitive functional groups, and achieve the late-stage functionalization of ten functional molecules that contain phenolic structures.

Original language	English
Pages (from-to)	223-226
Number of pages	4
Journal	Chemical Communications
Volume	59
Issue number	2
DOIs	https://doi.org/10.1039/d2cc05746h
State	Published - 30 Nov 2022

Access to Document

10.1039/d2cc05746h

Cite this

@article{6d826a6db9ac4669a91225a9649fedc9,

title = "Aqueous C-H aminomethylation of phenols by iodine catalysis",

abstract = "A transition-metal-free strategy regarding an iodine-sodium percarbonate catalysis to achieve the ortho-aminomethylation of phenols in aqueous media has been developed. This method can effectively broaden a wide range of phenols, tolerate sensitive functional groups, and achieve the late-stage functionalization of ten functional molecules that contain phenolic structures.",

author = "Zhou, {Zhi Hua} and Ben Wang and Yao Ding and Loh, {Teck Peng} and Tian, {Jie Sheng}",

note = "Publisher Copyright: {\textcopyright} 2023 The Royal Society of Chemistry.",

year = "2022",

month = nov,

day = "30",

doi = "10.1039/d2cc05746h",

language = "英语",

volume = "59",

pages = "223--226",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "2",

}

TY - JOUR

T1 - Aqueous C-H aminomethylation of phenols by iodine catalysis

AU - Zhou, Zhi Hua

AU - Wang, Ben

AU - Ding, Yao

AU - Loh, Teck Peng

AU - Tian, Jie Sheng

PY - 2022/11/30

Y1 - 2022/11/30

N2 - A transition-metal-free strategy regarding an iodine-sodium percarbonate catalysis to achieve the ortho-aminomethylation of phenols in aqueous media has been developed. This method can effectively broaden a wide range of phenols, tolerate sensitive functional groups, and achieve the late-stage functionalization of ten functional molecules that contain phenolic structures.

AB - A transition-metal-free strategy regarding an iodine-sodium percarbonate catalysis to achieve the ortho-aminomethylation of phenols in aqueous media has been developed. This method can effectively broaden a wide range of phenols, tolerate sensitive functional groups, and achieve the late-stage functionalization of ten functional molecules that contain phenolic structures.

UR - http://www.scopus.com/inward/record.url?scp=85144595155&partnerID=8YFLogxK

U2 - 10.1039/d2cc05746h

DO - 10.1039/d2cc05746h

M3 - 文章

C2 - 36484257

AN - SCOPUS:85144595155

SN - 1359-7345

VL - 59

SP - 223

EP - 226

JO - Chemical Communications

JF - Chemical Communications

IS - 2

ER -

Aqueous C-H aminomethylation of phenols by iodine catalysis

Abstract

Access to Document

Other files and links

Fingerprint

Cite this