Rearrangements of 14-mesyloxy-ent-beyer-15-enes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Ring c functionalised diterpenoids. Part V. Preparation and formolysis of (16S)-ent-12β-p-tolylsulphonyloxykaurane and the (16S)-ent-13-p-tolylsulphonyloxyatisanes
2. Ring c functionalised diterpenoids. Part VII. Formolysis of (16S)-ent-12α-p-tolylsulphonyloxykaurane
3. Biogenetic-like rearrangements of tetracyclic diterpenes
4. RingCfunctionalised diterpenoids. Part VI. Solvolysis of ent-methyl 12β-p-tolylsulphonyloxybeyeran-19-oate
5. Interconversion between hibaene and kaurene
Cited by 6 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. Skeletal Rearrangements of Rings C and D of the Kaurene and Beyerene Tetracyclic Diterpenoids;Journal of Chemical Research;2018-04
2. ChemInform Abstract: Rearrangements of 14-Mesyloxy-ent-beyer-15-enes.;ChemInform;2010-08-18
3. Connectivities in molecules by INADEQUATE: recent developments;Magnetic Resonance in Chemistry;2001
4. Ruthenium-Catalyzed Rearrangement of ent-14-(Benzoyloxy)-15,16-epoxybeyerane Diterpenes;Journal of Natural Products;1996-01-01
5. Diterpenoids;Natural Product Reports;1996
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