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2000
Volume 5, Issue 6
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

A new, convenient and high yield route to luzindole, the most commonly used melatonin receptor antagonist, is described. The new method involves the Sonogashira coupling reaction between 2-iodoaniline and 3-phenyl-1-propyne followed by cyclisation of the adduct formed, C-3 indole nitroolefination with 1-(dimethylamino)-2-nitroethylene/TFA, reduction to the respective tryptamine and finally acetylation.

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/content/journals/loc/10.2174/157017808785740561
2008-09-01
2025-09-06
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