An efficient and convenient formal synthesis of Jaspine B from d-xylose
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference50 articles.
1. Pachastrissamine, a Cytotoxic Anhydrophytosphingosine from a Marine Sponge, Pachastrissa sp.
2. Jaspines A and B: two new cytotoxic sphingosine derivatives from the marine sponge Jaspis sp.
3. Synthesis and biological properties of Pachastrissamine (jaspine B) and diastereoisomeric jaspines
4. The natural marine anhydrophytosphingosine, Jaspine B, induces apoptosis in melanoma cells by interfering with ceramide metabolism
5. Flexible and enantioselective access to jaspine B and biologically active chain-modified analogues thereof
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3. Research and Application of 2-Iodoxybenzoic Acid in Organic Synthesis;Chinese Journal of Organic Chemistry;2021
4. Synthetic analogues of marine cytotoxic jaspine B and its stereoisomers;Carbohydrate Research;2019-08
5. Enantioselective Stereodivergent Synthesis of Jaspine B and 4-epi-Jaspine B from Axially Chiral Allenols;Synlett;2018-12-06
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