Tetrahedron Letters p. 9627 - 9628 (1998)
Update date:2022-07-29
Topics:
Evans, P. Andrew
Murthy, V. Srinivasa
The 4-hydroxy buteneolide terminus 3, applicable to mucocin 1 and related annonaceous acetogenins, was prepared in an expeditious manner from the selenocarbonate 2 via an intramolecular acyl radical cyclization followed by an enantioselective Lewis-acid catalyzed Keck-allylation reaction.
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