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In situaminolysis of oxirane prepared from divinylacrbinol(1)via Sharpless asymmetricepoxidation was described where Ⅰ° and Ⅱ° amines were employed as nucleophiles.
In situaminolysis of oxirane prepared from divinylacrbinol (1) via Sharpless asymmetric oxidation was described where I ° and Ⅱ ° amines were employed as nucleophiles.