Synthesis of α-C-Galactosylceramide via Diastereoselective Aziridination: The New Immunostimulant 4′-epi-C-Glycoside of KRN7000
Author:
Affiliation:
1. Institute of Biomedical Sciences, Academia Sinica, No. 128 Academia Road, Section 2, Nankang, Taipei, Taiwan 11529
2. Department of Chemistry, National Central University, No. 300 Jhong-Da Road, Jhong-li, Taoyuan, Taiwan 32001
Funder
National Science Council Taiwan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b00090
Reference55 articles.
1. Agelasphins, novel α-galactosylceramides from the marine sponge Agelas mauritianus
2. Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus
3. Structure-Activity Relationship of .alpha.-Galactosylceramides against B16-Bearing Mice
4. Synthesis and stereochemistry of agelasphin-9b
5. CD1d-Restricted and TCR-Mediated Activation of V α 14 NKT Cells by Glycosylceramides
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