dc.contributor.author
Coussanes, Guilhem
dc.contributor.author
Vila, X.
dc.contributor.author
Diaba, Faïza
dc.contributor.author
Bonjoch i Sesé, Josep
dc.date.issued
2018-02-12T14:55:59Z
dc.date.issued
2018-02-12T14:55:59Z
dc.date.issued
2018-02-12T14:55:59Z
dc.identifier
https://hdl.handle.net/2445/119757
dc.description.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.
dc.format
application/pdf
dc.publisher
Georg Thieme Verlag Stuttgart · New York
dc.relation
Reproducció del document publicat a: https://doi.org/10.1055/s-0036-1588383
dc.relation
Synthesis, 2017, vol. 49, num. 07, p. 1481-1499
dc.relation
https://doi.org/10.1055/s-0036-1588383
dc.rights
cc-by-nc-nd (c) Coussanes, G. et al., 2017
dc.rights
http://creativecommons.org/licenses/by-nc-nd/3.0/es
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
dc.title
Radical Cyclization of Trichloroacetamides: Synthesis of Lactams
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion
