Synthesis and Isolation of Enantiomerically Enriched Cyclopenta[b]benzofurans Based on Products from Anodic Oxidation of 2,4-Dimethylphenol-Reference-Cited by-同舟云学术

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Synthesis and Isolation of Enantiomerically Enriched Cyclopenta[b]benzofurans Based on Products from Anodic Oxidation of 2,4-Dimethylphenol

Published:2015-06-25 Issue:22 Volume:2015 Page:4876-4882
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Mirion Michael,Andernach Lars,Stobe Caroline,Barjau Joaquin,Schollmeyer Dieter,Opatz Till,Lützen Arne,Waldvogel Siegfried R.

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference54 articles.

1. Constituents of thai medicinal plants—I aglaiol

2. X-Ray crystal structure of rocaglamide, a novel antileulemic 1H-cyclopenta[b]benzofuran from Aglaia elliptifolia

3. Cytostatic mechanism and antitumor potential of novel 1H-cyclopenta[b]benzofuran lignans isolated from Aglaiaelliptica

4. Structure Activity Relationships of Antiproliferative Rocaglamide Derivatives from Aglaia Species (Meliaceae)

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