Synthesis of 4-epi-Parviflorons A, C, and E: Structure–Activity Relationship Study of Antiproliferative Abietane Derivatives-Reference-Cited by-同舟云学术

Synthesis of 4-epi-Parviflorons A, C, and E: Structure–Activity Relationship Study of Antiproliferative Abietane Derivatives

Published:2019-02-22 Issue:6 Volume:84 Page:3239-3248
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Miyajima Yui¹,Saito Yohei¹,Takeya Munehisa¹,Goto Masuo²^ORCID,Nakagawa-Goto Kyoko¹²^ORCID

Affiliation:

1. School of Pharmaceutical Sciences, College of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, 920-1192, Japan

2. Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina 27599-7568, United States

Funder

Eshelman Institute for Innovation, University of North Carolina

Ministry of Education, Culture, Sports, Science and Technology

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b02832

Reference14 articles.

1. Diterpenoide Drüsenfarbstoffe aus Labiaten: 6 neuep-Chinomethane aus Plectranthus parviflorus WILLD

2. Drüsenfarbstoffe aus tropischen Labiaten: Parviflorone ausPlectranthus strigosusBENTH.

3. Total Synthesis of Antiproliferative Parvifloron F

4. An overview of triple-negative breast cancer

5. Synthesis of (+)-Hanagokenol A, (+)-Fortunins E, G, H, and (-)-Sugikurojin A from Abietic Acid

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