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制备前列环素和前列腺素类似物的新型合成策略——不走寻常路。

Novel synthetic strategies for the preparation of prostacyclin and prostaglandin analogues--off the beaten track.

作者信息

Sheddan Neil A, Czybowski Michael, Mulzer Johann

机构信息

Institut für Organische Chemie, Währingerstrasse 38, A-1090 Wien, Austria.

出版信息

Chem Commun (Camb). 2007 Jun 7(21):2107-20. doi: 10.1039/b617693n. Epub 2007 Mar 14.

Abstract

The recent increase in activity in the fields of neuroscience and life sciences has been mirrored by the design and synthesis of novel chemically and metabolically stable prostaglandin and prostacyclin analogues. Consequently, convenient and practical access to these important classes of compounds is greatly coveted. Various strategies for the preparation of prostacyclin, prostaglandin and isoprostane analogues are discussed, with particular focus on novel approaches developed in our own laboratories.

摘要

神经科学和生命科学领域近期活动的增加,反映在新型化学和代谢稳定的前列腺素和前列环素类似物的设计与合成上。因此,人们极其渴望能够方便、实用地获得这些重要类别的化合物。本文讨论了制备前列环素、前列腺素和异前列腺素类似物的各种策略,特别关注了我们自己实验室开发的新方法。

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