A unified, RCM anchored approach to spiro[4.5]decane-based sesquiterpenoids: Collective synthesis of (±)-α & β-vetispirenes, (±)-β-vetivone, (±)-agarospirol and (±)-hinesol
Author:
Funder
University Grants Commission
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference70 articles.
1. Synthesis of sesquiterpenes
2. Sesquiterpene biogenesis
3. Biogenetic implications of the antipodal sesquiterpenes of vetiver oil
4. Cationic rearrangements and cyclizations of diterpenoid olefins
5. Biosynthesis of sesquiterpenes
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1. Synthesis of Spiro[4.5]ecanes by Au(I)‐Catalyzed Vinylogous Conia Ene Reaction;European Journal of Organic Chemistry;2023-12-14
2. Construction of Spiro[4.5]decanes via Annulations of Azadienes with Nazarov Reagent and DFT Studies;Asian Journal of Organic Chemistry;2023-05-09
3. Recent Progress in the Synthesis of Sesquiterpenoid Involving Spirocyclic Carbon Framework;Natural Product Communications;2023-02
4. A Gold(I)‐Catalyzed Cyclization/Semipinacol Rearrangement Cascade of 1,6‐Enynes to Access Spiro[4.5]decanes and 7‐Azaspiro[4.5]decanes;Advanced Synthesis & Catalysis;2023-01-24
5. Spirocyclic Compounds in Fragrance Chemistry: Synthesis and Olfactory Properties;ChemPlusChem;2022-11
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