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Synthesis of functional amino acids bearing 1,3-dithiane modification

Ying Yang, Chao Wang*   

  1. Department of Medicinal Chemistry, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, China
  • Received:2010-11-07 Revised:2011-01-05 Online:2011-03-15 Published:2011-03-15
  • Contact: Chao Wang*

Abstract:

Two protected single amino acid chelates, Nα-Fmoc-Nε, Nε-di((2,2-dimethyl-1, 3-dithian-5-yl)methyl)-L-lysine (7) and Nα-Fmoc-Nε-(2,2-dimethyl-1,3-dithian-5-yl)methyl, Nε-Boc-L-lysine (9), were synthesized by modifying the side chain of lysine with 1,3-dithiane through direct reductive N-alkylation protocol. These amino acids have potential uses in peptide chemistry.

Key words: Amino acid chelate, 1,3-Dithiane, Reductive N-alkylation

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