Amino-acids condensations in the preparation of N alpha-9-fluorenylmethyloxycarbonylamino-acids with 9-fluorenylmethylchloroformate

Int J Pept Protein Res. 1983 Jul;22(1):125-8. doi: 10.1111/j.1399-3011.1983.tb02076.x.

Abstract

Synthesis of N alpha-9-fluorenylmethyloxycarbonyl (Fmoc) amino-acids by reaction of free amino-acids (glycine and alanine) with 9-fluorenylmethylchloroformate leads to formation of small amounts of Fmoc-dipeptide which are difficult to eliminate by crystallization. The alternative way to prepare Fmoc-amino-acids by reacting the Fmoc-chloride first with sodium azide and then with the free amino-acid eliminates this side reaction, at least for glycine and alanine.

MeSH terms

  • Amino Acids*
  • Chemical Phenomena
  • Chemistry
  • Fluorenes*
  • Oligopeptides / chemical synthesis*
  • Solubility

Substances

  • Amino Acids
  • Fluorenes
  • N(alpha)-fluorenylmethyloxycarbonylamino acids
  • Oligopeptides