Rapid access to 9-arylfluorene and spirobifluorene through Pd-catalysed C–H arylation/deaminative annulation-Reference-Cited by-同舟云学术

Rapid access to 9-arylfluorene and spirobifluorene through Pd-catalysed C–H arylation/deaminative annulation

Published:2022 Issue:43 Volume:58 Page:6280-6283
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Wu Yu¹,Wu Feng-Wei¹,Zhou Kun¹,Li Yiming²^ORCID,Chen Lei¹,Wang Shuang¹,Xu Zhen-Yuan¹,Lou Shao-Jie¹^ORCID,Xu Dan-Qian¹^ORCID

Affiliation:

1. Catalytic Hydrogenation Research Center, State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology, Key Laboratory of Green Pesticides and Cleaner Production Technology of Zhejiang Province, Zhejiang University of Technology, Hangzhou 310014, P. R. China

2. College of Biological, Chemical Sciences and Engineering, Jiaxing University, Jiaxing, 314001, China

Abstract

A rapid construction of 9-arylfluorenes and spirobifluorenes was developed through the tandem Pd-catalysed C–H arylation/demaminative annulation of 1,1-diarylmethylamines with aromatic iodides.

Funder

National Key Research and Development Program of China

Zhejiang University of Technology

Science and Technology Department of Zhejiang Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/CC/D2CC01355J

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