Alkali Metal-mediated Synthesis of 1- and 4-Substituted N-Alkyl-1,2,3,4-tetraidroisoquinolines
Academic Article
Publication Date:
2004
Short description:
Alkali Metal-mediated Synthesis of 1- and 4-Substituted N-Alkyl-1,2,3,4-tetraidroisoquinolines / Azzena, U.G., Pisano, L., Pittalis, M.. - In: HETEROCYCLES. - ISSN 0385-5414. - 63:2(2004), pp. 401-409.
abstract:
Reductive cleavage by electron transfer from Li or K metal of
1-alkoxy-substituted N-alkyltetrahydroisoquinolines led to the formation of
organometallic derivatives. Quenching of these intermediates with electrophilic
reagents afforded 1- or 4-substituted N-alkyl-1,2,3,4-tetrahydroisoquinolines,
depending upon the nature of the metal
1-alkoxy-substituted N-alkyltetrahydroisoquinolines led to the formation of
organometallic derivatives. Quenching of these intermediates with electrophilic
reagents afforded 1- or 4-substituted N-alkyl-1,2,3,4-tetrahydroisoquinolines,
depending upon the nature of the metal
Iris type:
1.1 Articolo in rivista
Keywords:
tetrahydroisoquinolines; reductive metalation; regioselectivity
List of contributors:
Azzena, Ugo Gavino; Pisano, L.; Pittalis, M.
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