4.8 Article

Enantioselective Total Synthesis of Spirofungins A and B

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ORGANIC LETTERS
卷 12, 期 19, 页码 4416-4419

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AMER CHEMICAL SOC
DOI: 10.1021/ol101961c

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  1. National Institute of General Medical Sciences [GM60567]

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The enantioselective total synthesis of spirofungins A (1) and B (2) is reported in 14 steps over the longest linear sequence. Key steps include the use of thiazolidinethione-mediated aldol reactions to assemble the major fragments and installation of the C1-C6 side chain using a cross metathesis reaction.

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