Preparation of helioporin D from the seco-pseudopterosin aglycone:: Revision of the stereostructure of helioporin D

被引：20

作者：

Geller, T ^{[1
]}

Jakupovic, J ^{[1
]}

Schmalz, HG ^{[1
]}

机构：

[1] Tech Univ Berlin, Inst Organ Chem, D-10623 Berlin, Germany

来源：

TETRAHEDRON LETTERS | 1998年 / 39卷 / 12期

关键词：

D O I：

10.1016/S0040-4039(98)00020-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A revised stereostructure for helioporin D was unequivocally established by its synthesis from the seco-pseudopterosin aglycone and by careful analysis of NMR data. As the corresponding benzodioxole derived from the pseudopterosin A aglycone was not identical with helioporin E, it was proven that helioporin D and E do not belong to the same stereochemical series. (C) 1998 Elsevier Science Ltd. All rights reserved.

引用

页码：1541 / 1544

页数：4

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