Synthetic study toward the total synthesis of solanoeclepin A
2017
Liu, Gang | Han, Jing-Chun | Li, Chuang-Chuang
A concise approach for the stereoselective construction of the oxa-pentacyclic core of solanoeclepin A has been developed by using the intramolecular Diels-Alder (IMDA) reaction from the furan-tethered dienophile.
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Bibliographic information
Tetrahedron
ISSN
0040-4020
Publisher
American Chemical Society
Other Subjects
Solanoeclepin a; Cycloaddition reactions; Stereochemistry; Oxabicyclo[2.2.1]heptane; Intramolecular diels-alder reaction
Language
English
Note
Pre-press version
Type
Journal Article; Text
2024-02-27
MODS
Data Provider
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