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Synthesis 2002(16): 2409-2415
DOI: 10.1055/s-2002-35218
DOI: 10.1055/s-2002-35218
PAPER
© Georg Thieme Verlag Stuttgart · New York
Application of 4-Alkoxy-1,1,1-trifluoro[chloro]alk-3-en-2-ones as Selective Protecting Groups of Amino Acids
Further Information
Received
8 November 2001
Publication Date:
04 November 2002 (online)
Publication History
Publication Date:
04 November 2002 (online)
Abstract
A convenient selective protection of the α-amino carboxyl group of amino acids bearing reactive side chain groups such as arginine, asparagine, glutamine, cysteine, histidine, serine and lysine, using 4-alkoxy-1,1,1-trifluoro[chloro]alk-3-en-2-ones is reported. The reactions were performed without esterification of the carboxyl group and N-deprotection was carried out using a six molar solution of hydrochloric acid.
Key words
ketones - fluorine - halogens - amino acids - protecting groups
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