Title of article
New building blocks for peptide and depsipeptide synthesis: hexafluoroacetone protected l-homoisoserine and d,l-homoisocysteine derivatives
Author/Authors
Radics، نويسنده , , Gلbor and Pires، نويسنده , , Raul and Koksch، نويسنده , , Beate and El-Kousy، نويسنده , , Salah M and Burger، نويسنده , , Klaus، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2003
Pages
4
From page
1059
To page
1062
Abstract
Efficient syntheses of l-homoisoserine and d,l-homoisocysteine derivatives starting from l-malic and d,l-thiomalic acid using hexafluoroacetone as protecting and activating agent are described. The new compounds are interesting building blocks for the preparation of non-natural peptides and depsipeptides as well as for the construction of new GABA derivatives.
Keywords
l-homoisoserine , l-homoisocysteine , Curtius rearrangement , peptide modification , d , Wolff rearrangement , GABA derivatives
Journal title
Tetrahedron Letters
Serial Year
2003
Journal title
Tetrahedron Letters
Record number
1660440
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