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Retracted: Enantioselective Radical Addition to Ketimines: A Synthetic Route Towards α,α‐Disubstituted α‐Amino Acids
Author(s) -
Kim Sang Yoon,
Kim Sung Jun,
Jang Doo Ok
Publication year - 2010
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201002071
Subject(s) - enantioselective synthesis , chemistry , nucleophile , stereocenter , imine , combinatorial chemistry , radical cyclization , aldehyde , addition reaction , alkene , reactivity (psychology) , chiral lewis acid , organic chemistry , protonation , nucleophilic addition , catalysis , medicine , ion , alternative medicine , pathology
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.