Your browser doesn't support javascript.
loading
Visible-Light-Driven N-Heterocyclic Carbene Catalyzed γ- and ϵ-Alkylation with Alkyl Radicals.
Dai, Lei; Xia, Zi-Hao; Gao, Yuan-Yuan; Gao, Zhong-Hua; Ye, Song.
Afiliação
  • Dai L; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
  • Xia ZH; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Gao YY; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
  • Gao ZH; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Ye S; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
Angew Chem Int Ed Engl ; 58(50): 18124-18130, 2019 Dec 09.
Article em En | MEDLINE | ID: mdl-31595644
ABSTRACT
The merging of photoredox catalysis and N-heterocyclic carbene (NHC) catalysis for γ- and ϵ-alkylation of enals with alkyl radicals was developed. The alkylation reaction of γ-oxidized enals with alkyl halides worked well for the synthesis γ-multisubstituted-α,ß-unsaturated esters, including those with challenging vicinal all-carbon quaternary centers. The synthesis of ϵ-multisubstituted-α,ß-γ,δ-diunsaturated esters by an unprecedented NHC-catalyzed ϵ-functionalization was also established.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article