Extension of the Bobbitt acetal cyclization to the elaboration of 1-hydroxymethyl-substituted simple tetrahydroisoquinolines. A new synthesis of calycotomine

Article abstract of DOI:10.1080/00397919308009802

Aromatic benzyloxymethyl ketones are convenient intermediates for the elaboration, via the Bobbitt acetal cyclization, of 1-hydroxymethyl-substituted simple tetrahydroisoquinolines, such as calycotomine and one bearing the 1,7,8-oxygenated substitution pa

Full text of DOI:10.1080/00397919308009802

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Synthetic Communications: An
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Organic Chemistry
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Extension of the Bobbitt Acetal
Cyclization to the Elaboration
of 1-Hydroxymethyl-
Substituted Simple
Tetrahydroisoquinolines. A New
Synthesis of Calycotomine
Teodoro S. Kaufman a
a Instituto de Química Orgánica de Síntesis
(CONICET-UNR), Facultad de Ciencias Bioquímicas y
Farmacéuticas, Casilla de Correo 991, 2000, Rosario,
Argentina
Published online: 23 Sep 2006.
To cite this article: Teodoro S. Kaufman (1993) Extension of the Bobbitt
Acetal Cyclization to the Elaboration of 1-Hydroxymethyl-Substituted
Simple Tetrahydroisoquinolines. A New Synthesis of Calycotomine, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 23:4, 473-486, DOI: 10.1080/00397919308009802
To link to this article: http://dx.doi.org/10.1080/00397919308009802
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