Chemie und Stereochemie der Iridoide, XIV. Aucubin und Scandosid aus Catalpol-Reference-Cited by-同舟云学术

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Chemie und Stereochemie der Iridoide, XIV. Aucubin und Scandosid aus Catalpol

Published:1990-07-12 Issue:7 Volume:1990 Page:715-717
ISSN:0170-2041
Container-title:Liebigs Annalen der Chemie
language:de
Short-container-title:Liebigs Ann. Chem.

Author:

Weinges Klaus,Ziegler Hans Jürgen

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Reference11 articles.

1. (6R,7R)−(−)-7-Hydroxy-3-oxabicyclo[4.3.0]non-1-en-9-on, ein leicht zugängliches und vielseitig verwendbares Zwischenprodukt

2. (6R, 7R)-(–)-7-Hydroxy-3-oxabicyclo[4.3.0]non-1-en-9-one, A Readily Accessible and Highly Versatile Intermediate

3. Application of the vilsmeier formylation in the synthesis of 11-13C labelled iridoids

4. Iridoids. A Review

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Iridoid Glycosides Isolated from Bellardia trixago Identified as Inhibitors of Orobanche cumana Radicle Growth;Toxins;2022-08-17

2. Anti-HIV Agents From Nature: Natural Compounds From Hypericum hircinum and Carbocyclic Nucleosides From Iridoids;Studies in Natural Products Chemistry;2018

3. The Vilsmeier Reaction of Non-Aromatic Compounds;Organic Reactions;2000-09-05

4. Preparation of Kingiside from Aucubin;European Journal of Organic Chemistry;2000-04

5. Ozonolysis of Protected Iridoid Glucosides;European Journal of Organic Chemistry;1998-02

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