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Studies on the Total Synthesis of Lactonamycin: Synthesis of the CDEF Ring System

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https://figshare.com/articles/dataset/Studies_on_the_Total_Synthesis_of_Lactonamycin_Synthesis_of_the_CDEF_Ring_System/3053797
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资源简介:
A concise and efficient synthesis of the tetracyclic CDEF ring system of lactonamycin (1) is described. The key step involved the Lewis acid mediated, intramolecular Friedel−Crafts acylation of carboxylic acid 6 to produce the tetracyclic CDEF core structure of target 1. The synthesis of 6 was carried out using a high-yielding Negishi coupling of benzyl bromide 7 with triflate 8, which was accessible in 11 steps and 31% overall yield on a multigram scale starting from trihydroxy acid 9.
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2006-10-13
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