Synthesis of 6-Trichloromethylphenanthridines by Transition Metal-Free Radical Cyclization of 2-Isocyanobiphenyls-Reference-Cited by-同舟云学术

Synthesis of 6-Trichloromethylphenanthridines by Transition Metal-Free Radical Cyclization of 2-Isocyanobiphenyls

Published:2016-05-31 Issue:12 Volume:81 Page:5202-5208
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Zhou Yuhan¹,Wu Changpeng¹,Dong Xiaoliang¹,Qu Jingping¹

Affiliation:

1. State Key Laboratory of Fine Chemicals, School of Pharmaceutical Science and Technology, Dalian University of Technology, Dalian 116024, P.R. China

Funder

Ministry of Education of the People's Republic of China

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b00885

Reference65 articles.

1. Synthesis of derivatives of NK109, 7-OH Benzo[c]phenanthridine alkaloid, and evaluation of their cytotoxicities and reduction-resistant properties

2. Structural Considerations of NK109, an Antitumor Benzo[c]phenanthridine Alkaloid

3. Revision of the Structure of Fagaridine Based on the Comparison of UV and NMR Data of Synthetic Compounds

4. Structure−Activity Relationship Studies of Phenanthridine-Based Bcl-XL Inhibitors

5. Esters and amides of 2,3-dimethoxy-8,9-methylenedioxy-benzo[i]phenanthridine-12-carboxylic acid: Potent cytotoxic and topoisomerase I-targeting agents

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