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Diastereoselective Ritter reactions of chiral secondary benzylic alcohols

  • Technical University of Munich

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

An acid-catalysed Ritter reaction of chiral secondary benzylic alcohols enables diastereoselective access to chiral amides, which represent inter alia valuable intermediates for the synthesis of chiral 1,2-diamines and β-amino acids.

Original languageEnglish
Pages (from-to)2130-2132
Number of pages3
JournalChemical Communications
Issue number16
DOIs
StatePublished - 2009

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