Oligomeric Flavanoids. Part 6. Evidence Supporting the Inversion of Absolute Configuration at 3-C Associated with Base Catalyzed A-/B-Ring Interchange of Precursors Having 2,3-trans-3,4-cis-Flavan-3-ol Constituent Units-Reference-Cited by-同舟云学术

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Oligomeric Flavanoids. Part 6. Evidence Supporting the Inversion of Absolute Configuration at 3-C Associated with Base Catalyzed A-/B-Ring Interchange of Precursors Having 2,3-trans-3,4-cis-Flavan-3-ol Constituent Units

Published:1989 Issue:2 Volume:28 Page:923
ISSN:0385-5414
Container-title:HETEROCYCLES
language:en
Short-container-title:HETEROCYCLES

Author:

Ferreira Daneel,P. Steynberg Jan,F. W. Burger Johann,A. Young Desmond,V. Brandt Edward

Publisher

The Japan Institute of Heterocyclic Chemistry

Subject

Organic Chemistry,Pharmacology,Analytical Chemistry

Cited by 23 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. Seco B-Type Oligomers from Pinus massoniana Expand the Procyanidin Chemical Space and Exhibit Dental Bioactivity;Journal of Natural Products;2022-11-16

2. 4-Arylflavan-3-ols as Proanthocyanidin Models: Absolute Configuration via Density Functional Calculation of Electronic Circular Dichroism;Journal of Natural Products;2009-11-30

3. Flavans and Proanthocyanidins;Flavonoids;2005-12-09

4. Circular dichroism, a powerful tool for the assessment of absolute configuration of flavonoids;Phytochemistry;2005-09

5. Condensed Tannins;Comprehensive Natural Products Chemistry;1999

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