Selective Aromatic  N ‐Substitution with  N ‐(4‐Tolyl)hydroxylamine by Addition of Polar Aprotic or Diethereal Solvent | Zendy

Takeuchi Hiroshi | Zendy; Tateiwa Junichi | Zendy; Hata Suguru | Zendy; Tsutsumi Keisuke | Zendy; Osaki Yoshinori | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Selective Aromatic N ‐Substitution with N ‐(4‐Tolyl)hydroxylamine by Addition of Polar Aprotic or Diethereal Solvent

Author(s) -

Takeuchi Hiroshi,

Tateiwa Junichi,

Hata Suguru,

Tsutsumi Keisuke,

Osaki Yoshinori

Publication year - 2003

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.200200576

Subject(s) - chemistry , trifluoroacetic acid , hydroxylamine , anisole , toluene , solvent , organic chemistry , amination , polar , electrophilic aromatic substitution , medicinal chemistry , catalysis , physics , astronomy

Amination of anisole and toluene with N ‐(4‐tolyl)hydroxylamine in trifluoroacetic acid was tuned to regioselectively provide the corresponding diarylamine by partial replacement of trifluoroacetic acid with a polar aprotic or a diethereal solvent. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research