| Literature DB >> 30848851 |
Masamichi Miyagawa1, Masaru Yoshida1, Yuki Kiyota1, Takahiko Akiyama1.
Abstract
An enantioselective Friedel-Crafts alkylation reaction of pyrroles and indoles with N-unprotected trifluoromethyl ketimines by use of chiral phosphoric acid provided α-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 α-trifluoromethylated amines were transformed without loss of enantioselectivity.Entities:
Keywords: chiral phosphoric acid; indoles; nucleophilic addition; pyrroles; trifluoromethyl ketimine
Year: 2019 PMID: 30848851 DOI: 10.1002/chem.201901020
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236