期刊
CHEMISTRYSELECT
卷 5, 期 48, 页码 15175-15179出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202003580
关键词
diastereoselective synthesis; C− H activation; fish; immunostimulant; spiro compounds
Filifolinol is a natural occurring spirodihydrobenzofuran isolated from the resinous exudates of Heliotropium filifolium, a Chilean endemic shrub. Filifolinol and some of its derivatives have shown interesting biological activities against pathogens that attack salmonid species. Whereas the synthesis of spirodihydrobenzofurans has been limited to the use of an ortho allylphenol unit herein we report a different approach based on a C-H activation/C-O cyclization reaction for the synthesis of analogues of Filifolinol. Moreover, a diastereoselective approach was developed using the different facial preference of hydride species and organolithium compounds towards cyclic ketones.
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