Highly efficient syntheses of the phytoalexin-elicitor active beta-(1 -> 3)-branched beta-(1 -> 6)-linked heptaglucose and its dodecyl glycoside
文献类型：期刊论文
| 作者 | Yi, YT; Zhou, ZX; Ning, J; Kong, FZ; Li, JQ |
| 刊名 | SYNTHESIS-STUTTGART
 |
| 出版日期 | 2003 |
| 期号 | 4页码:491-496 |
| 关键词 | Oligosaccharides Phytoalexin-elicitor Synthesis Glycosides Glycosylations |
| 英文摘要 | A highly efficient method for the synthesis of 3,6-branched gluco-oligosaccharides was developed by using 1,2-5,6-di-O-isopropylidene-alpha-D-glucofuranose, 2,3,4,6-tetra-O-benzoyl-alpha-D-glucopyranosyl trichloroacetimidate, and 6-O-acetyl-2,3,4-tri-O-benzoyl-alpha-D-glucopyranosyl trichloroacetimidate through a regio- and stereoselective manner. The beta-(1 --> 3)-branched beta-(1 --> 6)linked heptaglucose 1 and its dodecyl glycoside 2 having phytoalexin-elicitor activity were prepared using the,developed strategy. Bioassays showed that the phytoalexin-elicitor activity of the dodecyl beta-(1 --> 3)-branched beta-(1 --> 6)-linked hexaglucoside 2 is slightly more than that of the corresponding reducing end free heptaglucose 1. |
| WOS研究方向 | Chemistry |
| WOS记录号 | WOS:000181727400004 |
| 源URL | [http://ir.rcees.ac.cn/handle/311016/23821]  |
| 专题 | 生态环境研究中心_中国科学院环境生物技术重点实验室 |
| 推荐引用方式 GB/T 7714 | Yi, YT,Zhou, ZX,Ning, J,et al. Highly efficient syntheses of the phytoalexin-elicitor active beta-(1 -> 3)-branched beta-(1 -> 6)-linked heptaglucose and its dodecyl glycoside[J]. SYNTHESIS-STUTTGART,2003(4):491-496. |
| APA | Yi, YT,Zhou, ZX,Ning, J,Kong, FZ,&Li, JQ.(2003).Highly efficient syntheses of the phytoalexin-elicitor active beta-(1 -> 3)-branched beta-(1 -> 6)-linked heptaglucose and its dodecyl glycoside.SYNTHESIS-STUTTGART(4),491-496. |
| MLA | Yi, YT,et al."Highly efficient syntheses of the phytoalexin-elicitor active beta-(1 -> 3)-branched beta-(1 -> 6)-linked heptaglucose and its dodecyl glycoside".SYNTHESIS-STUTTGART .4(2003):491-496. |
入库方式： OAI收割
来源：生态环境研究中心
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