Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/119757
Title: Radical Cyclization of Trichloroacetamides: Synthesis of Lactams
Author: Coussanes, Guilhem
Vila, X.
Diaba, Faïza
Bonjoch i Sesé, Josep
Keywords: Lactames
Hidrurs
Lactams
Hydrides
Issue Date: Jan-2017
Publisher: Georg Thieme Verlag Stuttgart · New York
Abstract: Trichloroacetamides can act as radical precursors to synthesize nitrogen-containing heterocycles in a variety of processes, mainly involving atom transfer radical cyclizations (ATRC), mediated by Cu(I) or Ru(II) catalysts, and the hydride reductive method, employing either Bu3SnH or (Me3Si)3SiH, or recently NaBH3CN. Additionally, amine-mediated single-electron transfer cyclizations, as well as radical processes promoted by Ni, Fe, Mn, Ti, and Ag, have been developed.
Note: Reproducció del document publicat a: https://doi.org/10.1055/s-0036-1588383
It is part of: Synthesis, 2017, vol. 49, num. 07, p. 1481-1499
URI: http://hdl.handle.net/2445/119757
Related resource: https://doi.org/10.1055/s-0036-1588383
ISSN: 0039-7881
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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