Enantioselective radical addition to ketimines

A synthetic route towards α,α-disubstituted α-amino acids

Sang Yoon Kim, Sung Jun Kim, Doook Jang

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

A radical attack: In the presence of a protonated cinchonine derivative, radical addition reactions proceeded efficiently, providing a general approach to the synthesis of a diverse range of enantioenriched α,α- disubstituted α-amino acids.

Original languageEnglish
Pages (from-to)13046-13048
Number of pages3
JournalChemistry - A European Journal
Volume16
Issue number44
DOIs
Publication statusPublished - 2010 Nov 22

Fingerprint

Addition reactions
Amino acids
Derivatives
Amino Acids
cinchonine
ketimine

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)
  • Organic Chemistry

Cite this

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abstract = "A radical attack: In the presence of a protonated cinchonine derivative, radical addition reactions proceeded efficiently, providing a general approach to the synthesis of a diverse range of enantioenriched α,α- disubstituted α-amino acids.",
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Enantioselective radical addition to ketimines : A synthetic route towards α,α-disubstituted α-amino acids. / Kim, Sang Yoon; Kim, Sung Jun; Jang, Doook.

In: Chemistry - A European Journal, Vol. 16, No. 44, 22.11.2010, p. 13046-13048.

Research output: Contribution to journalArticle

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