4.6 Article

Enantioselective Friedel-Crafts Alkylation Reaction of Heteroarenes with N-Unprotected Trifluoromethyl Ketimines by Means of Chiral Phosphoric Acid

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 25, 期 22, 页码 5677-5681

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201901020

关键词

chiral phosphoric acid; indoles; nucleophilic addition; pyrroles; trifluoromethyl ketimine

资金

  1. MEXT, Japan
  2. JSPS [17H03060]
  3. Grants-in-Aid for Scientific Research [17H03060] Funding Source: KAKEN

向作者/读者索取更多资源

An enantioselective Friedel-Crafts alkylation reaction of pyrroles and indoles with N-unprotected trifluoromethyl ketimines by use of chiral phosphoric acid provided alpha-trifluoromethylated primary amines bearing chiral tetrasubstituted carbon centers in high yields and with high to excellent enantioselectivities. The present reaction is unique to N-unprotected trifluoromethyl ketimines. No reaction took place with N-p-methoxyphenyl (PMP)-substituted ketimine. Corresponding alpha-trifluoromethylated amines were transformed without loss of enantioselectivity.

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