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Biosci Biotechnol Biochem ; 88(7): 733-741, 2024 Jun 21.
Article in English | MEDLINE | ID: mdl-38653727

ABSTRACT

Synthesis of the A/D/E-ring core compounds of maoecrystal V was achieved. The key Diels-Alder reactions between tricyclic α-methylene lactones and Kitahara-Danishefsky dienes afforded the spirocyclic core compounds in a regioselective and stereoselective manner.


Subject(s)
Lactones , Stereoisomerism , Lactones/chemistry , Lactones/chemical synthesis , Cycloaddition Reaction , Chemistry Techniques, Synthetic , Diterpenes/chemical synthesis , Diterpenes/chemistry , Spiro Compounds/chemistry , Spiro Compounds/chemical synthesis , Molecular Structure
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