Fujita Ken-Ichi, Fujii Takeshi, Yamaguchi Ryohei
Graduate School of Human and Environmental Studies, Kyoto University, Kyoto 606-8501, Japan.
Org Lett. 2004 Sep 30;6(20):3525-8. doi: 10.1021/ol048619j.
[reaction: see text] A new efficient method for the N-heterocyclization of primary amines with diols catalyzed by a CpIr complex was developed. A variety of five-, six-, and seven-membered cyclic amines were synthesized in good to excellent yields with the formation of only water as a byproduct. A two-step asymmetric synthesis of (S)-2-phenylpiperidine was also achieved using (R)-1-phenylethylamine as a starting primary amine.
[反应:见正文] 开发了一种由CpIr配合物催化的伯胺与二醇进行N-杂环化反应的新高效方法。合成了多种五元、六元和七元环胺,产率良好至优异,且仅以水作为副产物生成。还使用(R)-1-苯乙胺作为起始伯胺实现了(S)-2-苯基哌啶的两步不对称合成。