Enantioselective radical addition to ketimines: A synthetic route towards α,α-disubstituted α-amino acids

Sang Yoon Kim, Sung Jun Kim, Doo Ok Jang

Research output: Contribution to journalArticlepeer-review

19 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

Bibliographical note

Funding Information:
This research was partly supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (NRF-2014R1A1A1005969) and Institute for Information & communications Technology Promotion (IITP) grant funded by the Korea government (MSIP) (No. R0190-16-2012).

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Organic Chemistry

Fingerprint

Dive into the research topics of 'Enantioselective radical addition to ketimines: A synthetic route towards α,α-disubstituted α-amino acids'. Together they form a unique fingerprint.

Cite this