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

Alkali Metal-mediated Synthesis of 1- and 4-Substituted N-Alkyl-1,2,3,4-tetraidroisoquinolines / Azzena, Ugo Gavino; Pisano, L.; Pittalis, M.. - In: HETEROCYCLES. - ISSN 0385-5414. - 63:2(2004), pp. 401-409.

Alkali Metal-mediated Synthesis of 1- and 4-Substituted N-Alkyl-1,2,3,4-tetraidroisoquinolines

UGO AZZENA;L. PISANO;
2004-01-01

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
2004
Alkali Metal-mediated Synthesis of 1- and 4-Substituted N-Alkyl-1,2,3,4-tetraidroisoquinolines / Azzena, Ugo Gavino; Pisano, L.; Pittalis, M.. - In: HETEROCYCLES. - ISSN 0385-5414. - 63:2(2004), pp. 401-409.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11388/57510
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