Aza-henry reaction of substituted nitroalkanes using α-formamidoaryl sulfones as N-acylimino equivalents
摘要：
Base-promoted elimination of p-toluenesulfinic acid from N-formamidoaryl sulfones leads to the corresponding N-acylimines that react with primary and secondary nitronate anions giving anti-β-formamido nitroderivatives in good yields and high diastereoselectivity.
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DOI：
10.1016/j.tetlet.2006.03.114
被引量：
年份：
2006
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