...
首页> 外文期刊>Journal of natural products >Xestoproxamines A-C from Neopetrosia proxima. Assignment of absolute stereostructure of bis-piperidine alkaloids by integrated degradation-CD analysis.
【24h】

Xestoproxamines A-C from Neopetrosia proxima. Assignment of absolute stereostructure of bis-piperidine alkaloids by integrated degradation-CD analysis.

机译:来自近新石楠的Xestoproxamines A-C。通过整合降解-CD分析确定双哌啶生物碱的绝对立体结构。

获取原文
获取原文并翻译 | 示例

摘要

The complete stereostructures of xestoproxamines A-C, from the Bahamian sponge Neopetrosia proxima, were assigned from spectroscopic analysis, including MS, 2D NMR, and integrated degradation-CD analysis. Two new CD application protocols are described for defining absolute configuration: one for allylic methyl groups in branched chains and a second for the heterocyclic core bis-piperidine with specific applicability to other members of this class alkaloids--known for their stereoheterogeneity--and tertiary cyclic amines in general.
机译:通过光谱分析,包括质谱,2D NMR和集成的降解CD分析,确定了来自巴哈马海绵Neopetrosia proxima的xestoproxamines A-C的完整立体结构。描述了两种用于定义绝对构型的新的CD应用方案:一种用于支链中的烯丙基甲基,另一种用于杂环核心双哌啶,这些化合物对此类生物碱的其他成员具有特殊的应用性(以立体异构性而著称),而三级环胺一般。

著录项

相似文献

  • 外文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号