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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Библиографическая информация
Tetrahedron
ISSN
0040-4020
Издатель
American Chemical Society
Другие темы
Stereochemistry; Solanoeclepin a; Intramolecular diels-alder reaction; Oxabicyclo[2.2.1]heptane; Cycloaddition reactions
Язык
Английский
Примечание
Pre-press version
Тип
Journal Article; Text
2024-02-27
MODS
Поставщик данных
Эту запись предоставил National Agricultural Library
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