Synthesis of sphingosine relatives, VII. Synthesis of anti-ulcerogenic cerebrosides isolated fromTetragonia tetragonoides
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Reference15 articles.
1. Synthesis of sphingosine relatives. Part VI. Stereocontrolled synthesis of (2R,3R,5R,13S,14R)-(+)-aplisiasphingosine, a marine terpenoid.
2. The Principles of Tetragonia tetragonoides Having an Antiulcerogenic Activity. I. Isolation and Identification of Sterylglucoside Mixture (Compound A)
3. The principles of Tetragonia tetragonoides having anti-ulcerogenic activity. II. Isolation and structure of cerebrosides.
4. Total synthesis and determination of absolute configuration of cerebroside B1b and its stereoisomers
5. Synthesis of (4,8,2,3,2')--2' -hydroxyhexadecanoyl-9-methyl-4,8-sphingadiemine, the ceramide portion of the fruiting-inducing cerebroside in a basidiomycete , and its (2,3)-isomer
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4. Efficient stereocontrolled synthesis of sphingadienine derivatives;Tetrahedron;2005-09
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