摘要
Three structurally defined QS-21-based immune adjuvant candidates (2a-2c) have been synthesized. Application of the two-stage activation glycosylation approach utilizing allyl glycoside building blocks improved the synthetic accessibility of the new adjuvants. The efficient synthesis and establishment of the stand-alone adjuvanticity of the examined synthetic adjuvant (2b) open the door to the pursuit of a new series of structurally defined QS-saponin-based synthetic adjuvants.
源语言 | 英语 |
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页(从-至) | 11525-11534 |
页数 | 10 |
期刊 | Journal of Organic Chemistry |
卷 | 78 |
期 | 22 |
DOI | |
出版状态 | 已出版 - 15 11月 2013 |
已对外发布 | 是 |