A biomimetic type expedient approach to the tricyclic core of xyloketals. Application to a short, stereocontrolled synthesis of alboatrin and a remarkable epi to natural isomerisation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Five Unique Compounds: Xyloketals from Mangrove Fungus Xylaria sp. from the South China Sea Coast
2. Xyloketal F: A Strong L -Calcium Channel Blocker from the Mangrove Fungus Xylaria sp. (#2508) from the South China Sea Coast
3. New Advances in the Field of Calcium Channel Antagonists: Cardiovascular Effects and Structure-Activity Relationships
4. Synthesis of Xyloketals, Natural Products from the Mangrove FungusXylaria sp
5. Total synthesis of ()-xyloketal D and its enantiomer Confirmation of absolute stereochemistry
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1. Synthesis and structural anomaly of xyloketals‐unique benzoxacycles: A review;Journal of Heterocyclic Chemistry;2020-10-09
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3. Total Synthesis of Xyloketals and Related Natural Product Alboatrin: Strategies and Tactics;ChemistrySelect;2019-08-19
4. Radical-induced expeditious stereoselective synthesis of 2-alkyl 3-allyl trans-2,3-dihydrobenzofurans (TADHBs);Synthetic Communications;2018-01-24
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