Organic Letters 2001-05-03

The first total synthesis of (+/-)-linderol A, a tricyclic hexahydrodibenzofuran constituent of Lindera umbellata bark, with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells.

M Yamashita, N Ohta, I Kawasaki, S Ohta

Index: Org. Lett. 3(9) , 1359-62, (2001)

Full Text: HTML

Abstract

[reaction in text] The first total synthesis of (+/-)-linderol A, a hexahydrodibenzofuran isolated from Lindera umbellata bark, with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells was achieved via a 20-step of reaction in 7.64% overall yield starting from 4,6-dimethoxysalicylaldehyde.

Related Compounds

Structure Name/CAS No. Articles
2-Hydroxy-4,6-dimethoxybenzaldehyde Structure 2-Hydroxy-4,6-dimethoxybenzaldehyde
CAS:708-76-9