Abstract
The condensation reaction of modified Reissert compounds with aldehydes was investigated. In the reaction of the N-ethoxycarbonyl Reissert analog 1b, ethoxycarbonyl group migration takes place and carbonates of 1-isoquinolylphenylcarbinols (2b, c) are formed. No alkoxycarbonyl group migration was observed in the case of the dihydro-Reissert derivative 6, but the cyclic urethane 7 and the amide 8 were obtained.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
19 articles.
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1. Heterocyclic monomers via reissert chemistry;Journal of Polymer Science Part A: Polymer Chemistry;2011-06-28
2. Reissert Compound;Comprehensive Organic Name Reactions and Reagents;2010-09-15
3. Synthesis of heterocyclic monomers via Reissert chemistry;Journal of Polymer Science Part A: Polymer Chemistry;2010-07-15
4. Isoquinoline Carboxylic Acids and Their Hydrogenated Derivatives;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
5. Organocatalytic asymmetric destruction of 1-benzylated Reissert compounds catalysed by quaternary cinchona alkaloids;Organic & Biomolecular Chemistry;2007