Synthetic study toward the total synthesis of solanoeclepin A
01 natural sciences
0104 chemical sciences
DOI:
10.1016/j.tet.2017.03.090
Publication Date:
2017-04-01T23:18:33Z
AUTHORS (3)
ABSTRACT
Abstract 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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