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-Reference-Cited by-同舟云学术

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

Published:2001-04-06 Issue:9 Volume:3 Page:1359-1362
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yamashita Masayuki¹,Ohta Nobukazu¹,Kawasaki Ikuo¹,Ohta Shunsaku¹

Affiliation:

1. Kyoto Pharmaceutical University, Misasagi-Nakauchicho 5, Yamashinaku, Kyoto 607-8414, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0157398

Reference8 articles.

1. A novel hexahydrodibenzofuran derivative with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells from Lindera umbellata bark.

2. One-Step Synthesis of 2-Substituted Cyclopenta[b]benzofuran-3-ol Derivatives from 3-Substituted Coumarins

3. A convenient synthesis of prenylated isoflavones : Synthesis of licoricone and related compounds.

4. Organoselenium chemistry. Conversion of ketones to enones by selenoxide syn elimination

5. Stereocontrolled synthesis of (±)-debromoaplysin and (±)-aplysin

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