Dearomative Iodocyclization of N-(o-Alkynyl)aryl Isoindole

Zhiqiong Tang; Fang Zhang; Tengfei Yao; Xun Shen Liu; Yuanyuan Liu; Lu Liu

doi:10.1021/acs.joc.2c00424

Dearomative Iodocyclization of N-(o-Alkynyl)aryl Isoindole

Zhiqiong Tang
, Fang Zhang
, Tengfei Yao
, Xun Shen Liu
, Yuanyuan Liu
, Lu Liu^*

^*此作品的通讯作者

化学与分子工程学院

East China Normal University

科研成果: 期刊稿件 › 文章 › 同行评审

5 引用（Scopus）

摘要

We present a dearomative iodocyclization of N-(o-alkynyl)aryl isoindole here, which affords various biologically active benzoindoleazine skeletons containing alkenyl iodine. The products can further undergo cycloaddition or coupling reactions to afford a series of highly functionalized N-fused polycyclic scaffolds.

源语言	英语
页（从-至）	7531-7535
页数	5
期刊	Journal of Organic Chemistry
卷	87
期	11
DOI	https://doi.org/10.1021/acs.joc.2c00424
出版状态	已出版 - 3 6月 2022

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10.1021/acs.joc.2c00424

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@article{98f63faeeff249b0bfebccc330870080,

title = "Dearomative Iodocyclization of N-(o-Alkynyl)aryl Isoindole",

abstract = "We present a dearomative iodocyclization of N-(o-alkynyl)aryl isoindole here, which affords various biologically active benzoindoleazine skeletons containing alkenyl iodine. The products can further undergo cycloaddition or coupling reactions to afford a series of highly functionalized N-fused polycyclic scaffolds.",

author = "Zhiqiong Tang and Fang Zhang and Tengfei Yao and Liu, \{Xun Shen\} and Yuanyuan Liu and Lu Liu",

year = "2022",

month = jun,

day = "3",

doi = "10.1021/acs.joc.2c00424",

language = "英语",

volume = "87",

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journal = "Journal of Organic Chemistry",

issn = "0022-3263",

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T1 - Dearomative Iodocyclization of N-(o-Alkynyl)aryl Isoindole

AU - Tang, Zhiqiong

AU - Zhang, Fang

AU - Yao, Tengfei

AU - Liu, Xun Shen

AU - Liu, Yuanyuan

AU - Liu, Lu

PY - 2022/6/3

Y1 - 2022/6/3

N2 - We present a dearomative iodocyclization of N-(o-alkynyl)aryl isoindole here, which affords various biologically active benzoindoleazine skeletons containing alkenyl iodine. The products can further undergo cycloaddition or coupling reactions to afford a series of highly functionalized N-fused polycyclic scaffolds.

AB - We present a dearomative iodocyclization of N-(o-alkynyl)aryl isoindole here, which affords various biologically active benzoindoleazine skeletons containing alkenyl iodine. The products can further undergo cycloaddition or coupling reactions to afford a series of highly functionalized N-fused polycyclic scaffolds.

UR - https://www.scopus.com/pages/publications/85131434070

U2 - 10.1021/acs.joc.2c00424

DO - 10.1021/acs.joc.2c00424

M3 - 文章

AN - SCOPUS:85131434070

SN - 0022-3263

VL - 87

SP - 7531

EP - 7535

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 11

ER -

Dearomative Iodocyclization of N-(o-Alkynyl)aryl Isoindole

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