One-pot synthesis of N-protected β-chiral amino alcohols

Research output: Contribution to journalArticle

10 Citations (Scopus)


N-tert-butyloxycarbonyl-S-benzyl-cysteine, N-fluorenylmethyloxycarbonyl-alanine-, S-trityl-cysteine-, O-tert-butyl-serine- and O-tertbutyl-tyrosine were converted to the corresponding alcohols via sodium borohydride reduction of their in situ formed methyl esters. Enantiopurity of the products was checked by chiral HPLC method.

Original languageEnglish
Pages (from-to)1815-1820
Number of pages6
JournalSynthetic Communications
Issue number11
Publication statusPublished - Jan 1 2003


  • Amino alcohols
  • Enantiopurity
  • Reduction

ASJC Scopus subject areas

  • Organic Chemistry

Fingerprint Dive into the research topics of 'One-pot synthesis of N-protected β-chiral amino alcohols'. Together they form a unique fingerprint.

  • Cite this