Total Synthesis of (−)-Oridonin: An Interrupted Nazarov Approach-Reference-Cited by-同舟云学术

Total Synthesis of (−)-Oridonin: An Interrupted Nazarov Approach

Published:2019-12-05 Issue:51 Volume:141 Page:20048-20052
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Kong Lingran¹,Su Fan¹,Yu Hang¹,Jiang Zhe¹,Lu Yandong¹,Luo Tuoping¹²^ORCID

Affiliation:

1. Key Laboratory of Bioorganic Chemistry and Molecular Engineering, Ministry of Education and Beijing National Laboratory for Molecular Science, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China

2. Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China

Funder

Peking University

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

National Natural Science Foundation of China

Center for Life Sciences

Beijing National Laboratory for Molecular Sciences

College of Chemistry and Molecular Engineering, Peking University

PKUAIC

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.9b12034

Reference60 articles.

1. Diterpenoids from Isodon species: an update

2. Oridonin, a new diterpenoid from Isodon species

3. Therapeutic Potential of Oridonin and Its Analogs: From Anticancer and Antiinflammation to Neuroprotection

4. Enmein-type diterpenoid analogs from natural kaurene-type oridonin: Synthesis and their antitumor biological evaluation

5. Novel Nitrogen-Enriched Oridonin Analogues with Thiazole-Fused A-Ring: Protecting Group-Free Synthesis, Enhanced Anticancer Profile, and Improved Aqueous Solubility

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