Autor: |
Zhang, Z., Yin, Z., Meanwell, N. A., Kadow, J. F., Wang, T. |
Zdroj: |
Organic Letters; September 2003, Vol. 5 Issue: 19 p3399-3402, 4p |
Abstrakt: |
Pretreatment of a symmetrical primary or secondary diamine with 9-BBN prior to the addition of an acyl chloride significantly suppressed undesired diacylation, and the product of monoacylation predominated. The reactive preference is interpreted as the result of a selective deactivation of one nitrogen atom of the diamine by 9-BBN. |
Databáze: |
Supplemental Index |
Externí odkaz: |
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