Protecting-Group-Free Syntheses of ent-Kaurane Diterpenoids: [3+2+1] Cycloaddition/Cycloalkenylation Approach-Reference-Cited by-同舟云学术

Protecting-Group-Free Syntheses of ent-Kaurane Diterpenoids: [3+2+1] Cycloaddition/Cycloalkenylation Approach

Published:2020-01-22 Issue:5 Volume:142 Page:2238-2243
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wang Jin¹²,Hong Benke¹²,Hu Dachao¹²,Kadonaga Yuichiro¹²^ORCID,Tang Ruyao¹²,Lei Xiaoguang¹²³^ORCID

Affiliation:

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

2. Department of Chemical Biology, Synthetic and Functional Biomolecules Center, Peking University, Beijing 100871, China

3. Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, China

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.9b13722

Reference75 articles.

1. Occurrence, Biological Activities and Synthesis of Kaurane Diterpenes and their Glycosides

2. Diterpenoids from Isodon species and their biological activities

3. Diterpenoids from Isodon species: an update

4. OPTICAL ROTATORY DISPERSION STUDIES. LVIII.1 THE COMPLETE ABSOLUTE CONFIGURATIONS OF STEVIOL, KAURENE AND THE DITERPENE ALKALOIDS OF THE GARRYFOLINE AND ATISINE GROUPS2

5. 1-Hydroxyditerpenes from Two New Zealand Liverworts, Paraschistochila pinnatifolia and Trichocolea mollissima

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