Study of Diels–Alder Reactions of Purpurogallin Tetraacetate with Various Dienophiles

ECSOC-25 Pub Date : 2021-11-14 DOI:10.3390/ecsoc-25-11707
Salima Dib, B. Mostefa-Kara, D. Villemin, N. Bar
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Abstract

: Purpurogallin or (6 E ,8 Z )-2,3,4,6-tetrahydroxy-5H-benzo[7]annulen-5-one is a benzotropo-lone possessing a dienic system and is known to inhibit TLR1/TLR2 activation pathway. We have recently described the easy green synthesis of purpurogallin from pyrogallol catalyzed by a copper complex or by vegetable oxidases. The purpurogalline was acetylated and the tetraacetate derivative thus obtained was engaged in a Diels Alder reaction with various dienophiles (benzoquinone, maleic anhydride, ethylmaleimide, phenylmaleimide, etc.). The results obtained will be presented and discussed.
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四乙酸紫癜没食子素与多种亲二酚反应的研究
: Purpurogallin或(6e, 8z)-2,3,4,6- tetra羟基- 5h -benzo[7]annulen-5-one是一种具有二烯系的苯并二酚类化合物,已知可抑制TLR1/TLR2激活途径。我们最近描述了用铜络合物或植物氧化酶催化邻苯三酚合成紫癜胆碱的简单绿色方法。将嘌呤没食碱乙酰化,得到的四乙酸酯衍生物与各种亲二酚(苯醌、马来酸酐、乙基马来酰亚胺、苯基马来酰亚胺等)进行Diels Alder反应。本文将介绍和讨论所得结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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