[4 + 2] Cyclization or Lossen Rearrangement: Rhodium-Catalyzed Divergent Synthesis of Carboline Derivatives with Anticancer Activity-Reference-Cited by-同舟云学术

[4 + 2] Cyclization or Lossen Rearrangement: Rhodium-Catalyzed Divergent Synthesis of Carboline Derivatives with Anticancer Activity

Published:2024-05-14 Issue:20 Volume:26 Page:4212-4217
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Lv Lijie¹,Zheng Jia¹,Xiao Yijie¹,Ni Dan¹,Luo Zhangshun¹,Gao Yunyun¹,Wei Yue¹^ORCID,He Yi¹,Nie Shenyou¹²^ORCID

Affiliation:

1. Basic Medicine Research and Innovation Center for Novel Target and Therapeutic Intervention (Ministry of Education), Institute of Life Sciences, Chongqing 400016, China

2. Department of Urology, the Second Affiliated Hospital, Chongqing Medical University, Chongqing 400016, China

Funder

Ministry of Science and Technology of the People's Republic of China

Natural Science Foundation of Chongqing Municipality

Chongqing Medical University

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c01050

Reference30 articles.

1. β-Carboline Alkaloids from the Seeds of Peganum harmala and Their Anti-HSV-2 Virus Activities

2. Design, Synthesis, and Biological Activity of Marinacarboline Analogues as STAT3 Pathway Inhibitors for Docetaxel-Resistant Triple-Negative Breast Cancer

3. A short entry into the pyrido[2,3-b]indole ring system. Synthesis of the tetracyclic segment of the marine antitumor agents: Grossularines-1 and -2

4. α-Carboline derivative TJY-16 inhibits tumor growth by inducing G2/M cell cycle arrest in glioma cells

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