Synthesis of 8α–Acetoxy–2β,3β–dihydroxy–13,14,15,16–tetranorlabdan–12–oic Acid
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919808005938
Reference7 articles.
1. Chemistry of the Podocarpaceae. LXXVI. 8,13-Epoxy-3-β-hydroxylabd-14-en-2-one and 8,13-Epoxy-2-hydroxylabda-1,14-dien-3-one, New Diterpenoids From Lagarostrobus colensoi
2. Chemistry of the Podocarpaceae. LXXV. The Conversion of 2-Oxomanoyl Oxide Into 2-oxo-γ-bicyclohomofarnesal
3. Synthetic microbial chemistry, XVII. Synthesis of the complement inhibitor (−)-K-76 and of related compounds
4. An Efficient Protocol for the Epoxidation of Acid-and Acid/Base-Sensitive Alkenes Withm-Chloroperoxybenzoic Acid
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. ChemInform Abstract: Synthesis of 8α-Acetoxy-2β,3β-dihydroxy-13,14,15,16-tetranorlabdan-12 -oic Acid.;ChemInform;2010-06-21
2. RECENT PROGRESS IN THE SYNTHESIS OF LABDANE DITERPENOIDS. A REVIEW;Organic Preparations and Procedures International;2008-08
3. Strategies and approaches for constructing 1-oxadecalins;Tetrahedron;2006-11
4. Diterpenoids (1998);Natural Product Reports;2000
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