4.8 Article

Direct asymmetric synthesis of β-amino ketones from sulfinimines (N-sulfinylimines).: Synthesis of (-)-indolizidine 209B

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卷 5, 期 26, 页码 5011-5014

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AMER CHEMICAL SOC
DOI: 10.1021/ol035981+

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  1. NIGMS NIH HHS [GM 51982] Funding Source: Medline

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[GRAPHICS] N-Sulfinyl beta-amino ketones, prepared directly from the potassium enolates of methyl ketones and enantiopure sulfinimines, are transformed in one pot to protected amino ketones, which are valuable chiral building blocks for the assembly of piperidines. The utility of this methodology is illustrated in a concise asymmetric synthesis of (-)-indolizidine 209B.

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