ISSN:
1573-8353
Source:
Springer Online Journal Archives 1860-2000
Topics:
Chemistry and Pharmacology
Notes:
Abstract Amides IV, which are converted to 1-diphenylmethyl-4,6,7-substituted 1,2,3,4-tetrahydroisoquinolines (II) by cyclization and subsequent reduction with lithium aluminum hydride, were obtained by condensation of diphenylacetyl chloride with the corresponding substituted phenylethylamines (III). Amines VI, the open analogs of the tetrahydroisoquinolines, were synthesized by reduction of IV.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00522582
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