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Synlett 2011(6): 831-833
DOI: 10.1055/s-0030-1259714
DOI: 10.1055/s-0030-1259714
LETTER
© Georg Thieme Verlag
Stuttgart ˙ New York
Unexpected Formation of Tetramethylguanidines by Reaction of Dimethylformamide with Fmoc-Protected Aminoamides
Further Information
Received
21 January 2011
Publication Date:
08 March 2011 (online)
Publication History
Publication Date:
08 March 2011 (online)
Abstract
Reactions of primary amines with Fmoc-protected amino acids or Fmoc deprotection of the resulting products in N,N-dimethylformamide gave tetramethylguanidines in variable yields as unexpected by-products.
Key words
guanidine - peptide synthesis - Fmoc protection - Fmoc deprotection - dimethylformamide
- Supporting Information for this article is available online:
- Supporting Information
- 1
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Fields G. Methods for Removal of the Fmoc Group, In Peptide Synthesis ProtocolsPennington MW.Dunn BM. Humana Press; New Jersey: 1994. p.17-27