First Asymmetric Total Synthesis and Insight into the Structure of Laurenidificin
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences; Osaka University; 1-6, Yamada-oka 565-0871 Suita, Osaka Japan
2. Graduate School of Science and Engineering; Yamaguchi University; 2-16-1 Tokiwadai 755-8611 Ube Japan
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference13 articles.
1. Laurenidificin, a new brominated C15-acetogenin from the marine red alga Laurencia nidifica
2. Structures of Halogenated Chamigrene Derivatives, Minor Constituents from the Red AlgaLaurencia nipponicaYamadan
3. A c-15 non-terpenoid from the red alga Laurencia okamurai
4. Stereocontrolled Synthesis of a Possible Stereoisomer of Laurenidificin and a Formal Total Synthesis of (+)-Aplysiallene Featuring a Stereospecific Ring Contraction
5. Synthesis of a Tetradehydro-Disorazole C1
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