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Reductive C2-Alkylation of Pyridine and Quinoline N-Oxides Using Wittig Reagents.
Han, Sangil; Chakrasali, Prashant; Park, Jihye; Oh, Hyunjung; Kim, Saegun; Kim, Kyuneun; Pandey, Ashok Kumar; Han, Sang Hoon; Han, Soo Bong; Kim, In Su.
Afiliação
  • Han S; School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
  • Chakrasali P; Bio and Drug Discovery Division, Korea Research Institute of Chemical Technology, Daejeon, 34114, Republic of Korea.
  • Park J; Department of Medicinal and Pharmaceutical Chemistry, University of Science and Technology, Daejeon, 34113, Republic of Korea.
  • Oh H; School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
  • Kim S; School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
  • Kim K; School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
  • Pandey AK; Bio and Drug Discovery Division, Korea Research Institute of Chemical Technology, Daejeon, 34114, Republic of Korea.
  • Han SH; Department of Medicinal and Pharmaceutical Chemistry, University of Science and Technology, Daejeon, 34113, Republic of Korea.
  • Han SB; School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
  • Kim IS; School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Angew Chem Int Ed Engl ; 57(39): 12737-12740, 2018 09 24.
Article em En | MEDLINE | ID: mdl-30070744
ABSTRACT
The ability to alkylate pyridines and quinolines is important for their further development as pharmaceuticals and agrochemicals, and for other purposes. Herein we describe the unprecedented reductive alkylation of pyridine and quinoline N-oxides using Wittig reagents. A wide range of pyridine and quinoline N-oxides were converted into C2-alkylated pyridines and quinolines with excellent site selectivity and functional-group compatibility. Sequential C-H functionalization reactions of pyridine and quinoline N-oxides highlight the utility of the developed method. Detailed labeling experiments were performed to elucidate the mechanism of this process.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2018 Tipo de documento: Article