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佩尔廷啶 A-C:来自夹竹桃属的大酚碱-大酚碱双吲哚和佩尔廷碱与马卡罗宁的绝对构型。

Perhentidines A-C: macroline-macroline bisindoles from Alstonia and the absolute configuration of perhentinine and macralstonine.

机构信息

Department of Chemistry, University of Malaya , 50603 Kuala Lumpur, Malaysia.

出版信息

J Nat Prod. 2012 May 25;75(5):942-50. doi: 10.1021/np300120p. Epub 2012 May 4.

Abstract

Three new bisindole alkaloids of the macroline-macroline type, perhentidines A-C (1-3), were isolated from the stem-bark extract of Alstonia macrophylla and Alstonia angustifolia. The structures of these alkaloids were established on the basis of NMR and MS analyses. The absolute configurations of perhentinine (4) and macralstonine (5) were established by X-ray diffraction analyses, which facilitated assignment of the configuration at C-20 in the regioisomeric bisindole alkaloids perhentidines A-C (1-3). A potentially useful method for the determination of the configuration at C-20 based on comparison of the NMR chemical shifts of the bisindoles and their acetate derivatives, in these and related bisindoles with similar constitution and branching of the monomeric units, is also presented.

摘要

从大青属和青藤属茎皮提取物中分离得到三种新的马罗林-马罗林型双吲哚生物碱,分别为佩亨丁 A-C(1-3)。这些生物碱的结构是基于 NMR 和 MS 分析确定的。通过 X 射线衍射分析确定了佩亨汀(4)和马罗林(5)的绝对构型,这有助于确定在结构类似的双吲哚生物碱佩亨丁 A-C(1-3)中,20 位的构型。还提出了一种基于双吲哚及其乙酰化物衍生物的 NMR 化学位移比较,来确定这些和相关的双吲哚中单体单元的构型和支化相似的 20 位构型的有用方法。

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