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Tetraethylphosphorodiamidate-Directed Metalation Group: Directed Ortho and Remote Metalation, Cross Coupling, and Remote Phospha Anionic Fries Rearrangement Reactions.
Patel, Jignesh J; Blackburn, Thomas; Alessi, Manlio; Sawinski, Hannah; Snieckus, Victor.
Afiliação
  • Patel JJ; Department of Chemistry, Queen's University, Kingston K7L 3N6, ON, Canada.
  • Blackburn T; Department of Chemistry, Queen's University, Kingston K7L 3N6, ON, Canada.
  • Alessi M; Department of Chemistry, Queen's University, Kingston K7L 3N6, ON, Canada.
  • Sawinski H; Department of Chemistry, Queen's University, Kingston K7L 3N6, ON, Canada.
  • Snieckus V; Department of Chemistry, Queen's University, Kingston K7L 3N6, ON, Canada.
Org Lett ; 22(10): 3860-3864, 2020 May 15.
Article em En | MEDLINE | ID: mdl-32319779
ABSTRACT
The linked directed ortho and remote metalation (DoM and DreM) and cross-coupling reactions of aryl phosphorodiamidates (Ar-OP(O)(NEt2)2) is reported. The o-iodo and o-boronato aryl tetraethylphosphorodiamidates 3, prepared by DoM, undergo orthogonal Ni- and Pd-catalyzed Suzuki-Miyaura cross coupling to furnish biaryls 4 and 5 in good to excellent yields. Silicon group protection of biaryl 4 via DoM followed by previously unobserved DreM phospha anionic Fries rearrangement affords biaryls 11 which, under acidic conditions, furnish oxaphosphorine oxides 12.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Ano de publicação: 2020 Tipo de documento: Article