摘要
A divergent strategy for the synthesis of 1-aryl- and 2-aryl-2-iminoimidazolidines is presented. Cyclization of N-Boc-N%26apos;-aryl-N %26apos;%26apos;-(2-hydroxyethyl)guanidines in the presence of methanesulfonyl chloride and triethylamine or sodium hydride at 0 degrees C affords the corresponding 2-iminoimidazolidines in good yields.
- 出版日期2012-8-22