Tetrahedron Letters p. 465 - 469 (2000)
Update date:2022-07-30
Topics: Synthesis Antagonist Total synthesis
Katoh, Tadashi
Ohmori, Osamu
An efficient synthesis of (±)-geodin [(±)-2] corresponding to the spirocoumaranone subunit of Sch 202596 (1) was accomplished in a convergent manner by utilizing coupling reaction of the aryl aldehyde 5 with the aryl bromide 6 and oxidative spirocyclization of the benzophenone 4 as the key steps. The aromatic segments 5 and 6 were prepared from commercially available methyl 3,5-dihydroxybenzoate (7) and 5-methylresorcinol (8), respectively.
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Doi:10.1021/ol005585g
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(2000)