Enantioselective total synthesis of doliculide, a potent cytotoxic cyclodepsipeptide of marine origin and structure-cytotoxicity relationships of synthetic doliculide congeners-Reference-Cited by-同舟云学术

Enantioselective total synthesis of doliculide, a potent cytotoxic cyclodepsipeptide of marine origin and structure-cytotoxicity relationships of synthetic doliculide congeners

Published:1994-01 Issue:45 Volume:50 Page:12853-12882
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Hiroyuki Ishiwata,Hiroki Sone,Hideo Kigoshi,Kiyoyuki Yamada

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference29 articles.

1. Isolation and stereostructure of doliculide, a cytotoxic cyclodepsipeptide from the Japanese sea hare Dolabella auricularia

2. Total Synthesis of Doliculide, a Potent Cytotoxic Cyclodepsipeptide from the Japanese Sea Hare Dolabella auricularia

3. Stereostructures of geodiamolides A and B, novel cyclodepsipeptides from the marine sponge Geodia sp

4. Geodiamolides C to F, new cytotoxic cyclodepsipeptides from the marine sponge Pseudaxinyssa sp.

5. Jaspamide, a modified peptide from a Jaspis sponge, with insecticidal and antifungal activity

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