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The Journal of organic chemistry

Intramolecular imino Diels− Alder reaction: progress toward the synthesis of Uncialamycin

S Desrat, P van de Weghe

文献索引:Desrat, Sandy; Van De Weghe, Pierre Journal of Organic Chemistry, 2009 , vol. 74, # 17 p. 6728 - 6734

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被引用次数: 32

摘要

In 2005, Davies, Andersen, and co-workers disclosed the uncialamycin 1, a new “enediyne” natural product isolated from an undescribed streptomycete obtained from the surface of a lichen Cladonia uncialis.(1) The first biological evaluations showed that 1 possesses potent in vitro antibacterial activity against Staphylococcus aurens, Escheridia coli, and Burkholderia apia. Despite the small amount of product available (∼300 μg were isolated) the structure of 1 ...