Reactivity of Chiral Sesquiterpene Synthons Obtained by the Degradation of Maslinic Acid from Olive‐Pressing Residues
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397910600773858
Reference19 articles.
1. Terpenoid precursors via steroid degradation: synthesis of (–)-warburganal
2. Chemistry of zamoranic acid. Part V Homochiral semisyntheses of active drimanes: Pereniporin B, polygodial and warburganal
3. Synthesis of wiedendiol-A and wiedendiol-B from labdane diterpenes
4. The synthesis of Ambrox®-like compounds starting from (+)-larixol. Part 2
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1. (+)-Larixol and Larixyl Acetate: Syntheses, Phytochemical Studies and Biological Activity Assessments;Chemistry Journal of Moldova;2021-06
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3. Maslinic acid derivatives induce significant apoptosis in b16f10 murine melanoma cells;European Journal of Medicinal Chemistry;2011-12
4. Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry;Chemistry & Biodiversity;2010-02
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