Synthesis of Trans ‐4 a ,12 b /3,4‐Dihydrodibenzo[ f , h ]quinolin‐2(1 H )‐Ones and Dibenzo[ f , h ]quinolin‐2(1 H )‐Ones via Irradiation of 6‐Biphenylpyridine‐2(1 H )‐Ones-Reference-Cited by-同舟云学术

Synthesis of Trans ‐4 a ,12 b /3,4‐Dihydrodibenzo[ f , h ]quinolin‐2(1 H )‐Ones and Dibenzo[ f , h ]quinolin‐2(1 H )‐Ones via Irradiation of 6‐Biphenylpyridine‐2(1 H )‐Ones

Published:2021-06-04 Issue:14 Volume:363 Page:3554-3559
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Sui Jingzhi¹,He Yun¹,Wang Tao¹^ORCID,Liang Yong¹²,Zhang Zunting¹

Affiliation:

1. Key Laboratory of Applied Surface and Colloid Chemistry (Ministry of Education), School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710119 People's Republic of China

2. Department of Molecular Medicine Beckman Research Institute of City of Hope Duarte California 91010 United States

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202100509

Reference23 articles.

1. Antitumor Agents. 272. Structure−Activity Relationships and In Vivo Selective Anti-Breast Cancer Activity of Novel Neo-tanshinlactone Analogues

2. Correction: Continuous flow photochemistry as an enabling synthetic technology: synthesis of substituted-6(5H)-phenanthridinones for use as poly(ADP-ribose) polymerase inhibitors