4.8 Article

Kinetic Resolution of 2-Substituted Indolines by N-Sulfonylation using an Atropisomeric 4-DMAP-N-oxide Organocatalyst

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 56, 期 21, 页码 5760-5764

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201700977

关键词

asymmetric catalysis; indoline; kinetic resolution; organocatalysis; sulfonylation

资金

  1. EPSRC
  2. Institute of Chemical Biology (ICB, Imperial College London)
  3. SCI (Messel Scholarship)

向作者/读者索取更多资源

The first catalytic kinetic resolution by N-sulfonylation is described. 2-Substituted indolines are resolved (s=2.6-19) using an atropisomeric 4-dimethylaminopyridine-N-oxide (4-DMAP-N-oxide) organocatalyst. Use of 2-isopropyl-4-nitrophenylsulfonyl chloride is critical to the stereodiscrimination and enables facile deprotection of the sulfonamide products with thioglycolic acid. A qualitative model that accounts for the stereodiscrimination is proposed.

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