Modular Tandem Mizoroki‐Heck/Reductive Heck Reactions to Construct Fluorenes from Cyclic Diaryliodoniums-Reference-Cited by-同舟云学术

Modular Tandem Mizoroki‐Heck/Reductive Heck Reactions to Construct Fluorenes from Cyclic Diaryliodoniums

Published:2020-11-19 Issue:1 Volume:363 Page:222-226
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Peng Xiaopeng¹²,Yang Yang²³,Luo Bingling²,Wen Shijun²,Huang Peng²

Affiliation:

1. School of Pharmaceutical Sciences Zhaoqing Medical College Zhaoqing 526000 People's Republic of China

2. Sun Yat-sen University Cancer Center State Key Laboratory of Oncology in South China Collaborative innovation Center for Cancer Medicine Sun Yat-sen University Guangzhou 510060 People's Republic of China

3. School of Pharmaceutical Science Sun Yat-sen University Guangzhou 510006 People's Republic of China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202001080

Reference57 articles.

1. An investigation into the formation of N- [2-(dimethylamino)ethyl]acridine-4-carboxamide (DACA) and 6-[2-(dimethylamino)ethylamino]- 3-hydroxy-7H-indeno[2,1-C]quinolin-7-one dihydrochloride (TAS-103) stabilised DNA topoisomerase I and II cleavable complexes in human leukaemia cells

3. Candidate anti-Aβ fluorene compounds selected from analogs of amyloid imaging agents

4. A fluorene-core-based electron acceptor for fullerene-free BHJ organic solar cells—towards power conversion efficiencies over 10%

5. A New Mechanism of 6-((2-(Dimethylamino)ethyl)amino)-3-hydroxy-7H-indeno(2,1-c)quinolin-7-one Dihydrochloride (TAS-103) Action Discovered by Target Screening with Drug-Immobilized Affinity Beads

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