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

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:2003-01-07 Issue:4 Volume:68 Page:1216-1224
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yamashita Masayuki¹,Ohta Nobukazu¹,Shimizu Takashi¹,Matsumoto Kayoko¹,Matsuura Yoko¹,Kawasaki Ikuo¹,Tanaka Tetsuaki¹,Maezaki Naoyoshi¹,Ohta Shunsaku¹

Affiliation:

1. Kyoto Pharmaceutical University, Misasagi-Nakauchicho 5, Yamashinaku, Kyoto 607-8414, Japan, and Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo020619e

Reference16 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 novel tandem reaction of 3-substituted coumarins with two equivalents of dimethylsulfoxonium ylide to 2-substituted cyclopenta[b]benzofuran-3-ol derivatives

4. 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

5. Reductions via Boranes: A New, Convenient Method for the Preparation of 3-Substituted Esters and Thioesters of 3,4-Dihydrocoumarin

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