Asymmetric synthesis of a 3,4-substituted pyrrolidine by l-proline catalyzed direct enolexo aldolization
摘要：
The asymmetric synthesis of a 3,4-substituted N-tosyl pyrrolidine has been achieved by using l-proline catalyzed 5-enolexo aldolization with high enantio and diastereoselectivity.
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DOI：
10.1016/j.tetasy.2007.05.004
被引量：
年份：
2007
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