Hydrogen-Transfer-Mediated N-Arylation of Naphthols Using Indolines as Hydrogen Donors-Reference-Cited by-同舟云学术

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Hydrogen-Transfer-Mediated N-Arylation of Naphthols Using Indolines as Hydrogen Donors

Published:2019-11-29 Issue:2 Volume:85 Page:508-514
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chen Xiuwen¹^ORCID,Yang Zhihai¹,Chen Xuyan¹,Liang Wanyi¹,Zhu Zhongzhi¹,Xie Feng¹,Li Yibiao¹^ORCID

Affiliation:

1. School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, China

Funder

National innovation and entrepreneurship training program for college students

Jiangmen City Science and Technology Basic Research Project

Science Foundation for Young Teachers of Wuyi University

Foundation for Young Talents

Foundation of the Department of Education of Guangdong Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b02558

Reference50 articles.

1. An efficient, mild and selective Ullmann-type N -arylation of indoles catalysed by Pd immobilized on amidoxime-functionalized mesoporous SBA-15 as heterogeneous and recyclable nanocatalyst

2. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit (July 1997 to December 1998)

3. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit

4. Novel Antipsychotic Agents with Dopamine Autoreceptor Agonist Properties: Synthesis and Pharmacology of 7-[4-(4-Phenyl-1-piperazinyl)butoxy]-3,4-dihydro-2(1H)-quinolinone Derivatives

5. 1,2- and 1,4-Additions of 2-Alkynylcyclohexadienimines with Aromatic Amines To Access 4-Amino-N-arylindoles and -azepinoindoles

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