Iodine-Catalyzed Three-Component Cascade Reaction for the Synthesis of Substituted 2‑Phenylnaphtho[1,3]selenazoles under Transition-Metal-Free Conditions

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成果类型：

期刊论文

作者：

Chen, Wenqi;Zhu, Xiaoming;Wang, Fei;Yang, Yuan;Deng, Guobo*;...

通讯作者：

Deng, Guobo;Liang, Yun

作者机构：

[Wang, Fei; Yang, Yuan; Deng, Guobo; Liang, Yun; Chen, Wenqi] Hunan Normal Univ, Natl & Local Joint Engn Lab New Petrochem Mat & F, Key Lab Assembly & Applicat Organ Funct Mol Hunan, Minist Educ,Key Lab Chem Biol & Tradit Chinese Me, Changsha 410081, Hunan, Peoples R China.

[Zhu, Xiaoming] Hengyang Normal Univ, Coll Chem & Mat Sci, Hunan Prov Univ Key Lab Funct Organometall Mat, Key Lab Funct Met Organ Cpds Hunan Prov, Hengyang 421008, Hunan, Peoples R China.

通讯机构：

[Deng, GB; Liang, Y] H

Hunan Normal Univ, Natl & Local Joint Engn Lab New Petrochem Mat & F, Key Lab Assembly & Applicat Organ Funct Mol Hunan, Minist Educ,Key Lab Chem Biol & Tradit Chinese Me, Changsha 410081, Hunan, Peoples R China.

语种：

英文

期刊：

JOURNAL OF ORGANIC CHEMISTRY

ISSN：

0022-3263

年：

2020

卷：

期：

页码：

3349-3357

DOI：

10.1021/acs.joc.9b03154

基金类别：

National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21602057, 21572051, 21901071, 21971061]; Opening Fund of Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research (Ministry of Education of China)Ministry of Education, China; Hunan Normal University [KLCBTCMR201707, KLCBTCMR201708]; Science and Technology Planning Project of Hunan Province [2018TP1017]; Hong Kong Scholars program [XJ2017009]

机构署名：

本校为其他机构

院系归属：

化学与材料科学学院

摘要：

An efficient molecular iodine-catalyzed three-component cascade reaction for the construction of 2-phenylnaphtho[2,1-d]selenazoles from naphthalen-2-amine, aldehydes, and selenium powder has been developed. The present approach has the advantages of metal-free conditions, simple operation, and available raw materials. Moreover, the mechanism of the study pro...

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Iodine-Catalyzed Three-Component Cascade Reaction for the Synthesis of Substituted 2‑Phenylnaphtho[1,3]selenazoles under Transition-Metal-Free Conditions

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