4.7 Article

Synthesis of unsaturated organotrifluoroborates via Wittig and Horner-Wadsworth-Emmons olefination

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JOURNAL OF ORGANIC CHEMISTRY
卷 71, 期 16, 页码 6135-6140

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AMER CHEMICAL SOC
DOI: 10.1021/jo060863w

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  1. NIGMS NIH HHS [GM 35249] Funding Source: Medline

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The stereoselective synthesis of unsaturated organotrifluoroborates by using the Wittig and Horner-Wadsworth-Emmons olefination is described. These reactions were general for both alkyl- and aryltrifluoroborates. The synthesis of di- and trisubstituted olefins was achieved by using formyl- and acetyl-substituted organotrifluoroborates. The products were isolated in moderate to excellent yield. The Wittig reaction with nonstabilized ylides was performed under salt free conditions in most cases to obtain the Z-isomer. The E-isomer was accessed by using preformed stabilized ylides. The Horner-Wadsworth-Emmons reaction also gave the E-isomer as expected.

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