| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1388128 | Carbohydrate Research | 2016 | 42 Pages |
Abstract
Conformationally constrained sphingolipids such as anhydrophytosphingosines represented by jaspine B (also known as pachastrissamine) and its stereoisomers have become an attractive and timely target for total synthesis due to their significant biological activity as well as the unique structures. This review article describes the biological activity and chemistry of the natural jaspine B and its seven stereoisomers.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Miroslava Martinková, Jozef Gonda,