Stereoselective synthesis of (3S,4R)-3,4-dimethyl-(S)-glutamine and the absolute stereochemistry of the natural product from papuamides and callipeltin-Reference-Cited by-同舟云学术

Stereoselective synthesis of (3S,4R)-3,4-dimethyl-(S)-glutamine and the absolute stereochemistry of the natural product from papuamides and callipeltin

Published:2001-06 Issue:9 Volume:12 Page:1353-1358
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Okamoto Naoki,Hara Osamu,Makino Kazuishi,Hamada Yasumasa

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference17 articles.

1. Papuamides A−D, HIV-Inhibitory and Cytotoxic Depsipeptides from the Sponges Theonella mirabilis and Theonella swinhoei Collected in Papua New Guinea

2. Callipeltin A, an Anti-HIV Cyclic Depsipeptide from the New Caledonian Lithistida Sponge Callipelta sp.

3. Progress toward the Total Synthesis of Callipeltin A (I): Asymmetric Synthesis of (3S,4R)-3,4-Dimethylglutamine

4. New methods and reagents in organic synthesis. 83. Stereoselective total synthesis of AI-77-B, a gastroprotective substance from Bacillus pumilus AI-77

5. Efficient total synthesis of AI-77-B, A gastroprotective substance from bacillus pumilus AI-77

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