Unexpected course of the reaction of aromatic aldehydes on lithiatedN,N-dimethyl o-(3-quinolyl)carbamate
Author:
Publisher
Wiley
Subject
Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.5570240553/fullpdf
Reference5 articles.
1. The directed ortho lithiation of O-aryl carbamates. An anionic equivalent of the Fries rearrangement
2. Directed ortho metalation of O-pyridyl carbamates. Regiospecific entries into polysubstituted pyridines
3. A. Godard and G. Queguiner, next publication.
4. The 1H nmr signal of CH-O appears at 5.8 ppm in benzhydrol and at 6.8 ppm in benzhydrol acetate.
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3. Solvent-Free Synthesis of 1-(Hydroxyquinolyl)- and 1-(Hydroxyisoquinolyl)-1,2,3,4-tetrahydroisoquinolines by Modified Mannich Reaction;Synthesis;2011-02-03
4. Directed ortho-lithiation of chloroquinolines. Application to synthesis of 2,3-disubstituted quinolines;Journal of Heterocyclic Chemistry;2009-03-12
5. Microwave-Assisted One-Pot Synthesis of (Aminoalkyl)naphthols and (Aminoalkyl)quinolinols by Using Ammonium Carbamate or Ammonium Hydrogen Carbonate as Solid Ammonia Source;Synthesis;2009-02-02
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