Convergent Route to ent-Kaurane Diterpenoids: Total Synthesis of Lungshengenin D and 1α,6α-Diacetoxy-ent-kaura-9(11),16-dien-12,15-dione
Author:
Affiliation:
1. State Key Laboratory of Bioorganic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China
Funder
National Natural Science Foundation of China
Chinese Academy of Sciences
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.7b00140
Reference68 articles.
1. OPTICAL ROTATORY DISPERSION STUDIES. LVIII.1 THE COMPLETE ABSOLUTE CONFIGURATIONS OF STEVIOL, KAURENE AND THE DITERPENE ALKALOIDS OF THE GARRYFOLINE AND ATISINE GROUPS2
2. Occurrence, Biological Activities and Synthesis of Kaurane Diterpenes and their Glycosides
3. Diterpenoids from Isodon species and their biological activities
4. The Total Synthesis ofIsodonDiterpenes
5. Constructive innovation of approaching bicyclo[3.2.1]octane in ent-kauranoids
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