The efficient stereoselective synthesis of (2S,3R,4S,5S,6S,11E)-3-amino-6-methyl-12-(4-methoxyphenyl)-2,4,5-trihydroxydodec-11-enoic acid (AMMTD), a component of microsclerodermins of marine sponge origin, as its protected form-Reference-Cited by-同舟云学术

The efficient stereoselective synthesis of (2S,3R,4S,5S,6S,11E)-3-amino-6-methyl-12-(4-methoxyphenyl)-2,4,5-trihydroxydodec-11-enoic acid (AMMTD), a component of microsclerodermins of marine sponge origin, as its protected form

Published:1999-04 Issue:16 Volume:40 Page:3187-3190
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sasaki Shigekazu,Hamada Yasumasa,Shioiri Takayuki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference9 articles.

1. Microsclerodermins A and B. Antifungal Cyclic Peptides from the Lithistid Sponge Microscleroderma sp.

2. Microsclerodermins C - E, antifungal cyclic peptides from the lithistid marine sponges Theonella sp. and Microscleroderma sp.

3. Total Synthesis of Antillatoxin, an Ichthyotoxic Cyclic Lipopeptide, Having the Proposed Structure. What Is the Real Structure of Antillatoxin?

4. A part of this work was presented at the First International Peptide Symposium held in Kyoto, Japan,1997

5. at the 35th Japanese Peptide Symposium held in Saga, Japan,1998

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