Title of article
Conformationally restricted analogues of both (S)-β-homoserine and (S)-aspartic acid from chiral 3-acylamino pyrrolidin-2-ones
Author/Authors
Roberta Galeazzi، نويسنده , , Gianluca Martelli، نويسنده , , Mario Orena، نويسنده , , Samuele Rinaldi، نويسنده , , Piera Sabatino، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
9
From page
5465
To page
5473
Abstract
Starting from chiral 3,4-trans-disubstituted pyrrolidin-2-ones and , obtained from a Baylis–Hillman adduct, conformationally restricted analogues of both (S)-β-homoserine, , and (S)-aspartic acid, , were synthesized, respectively, and these compounds are suitable either for introduction in peptidomimetics or for synthesis of novel β-foldamers.
Keywords
Amino acids , Conformational constrictions , Baylis–Hillman , Analogues , peptidomimetics
Journal title
Tetrahedron
Serial Year
2005
Journal title
Tetrahedron
Record number
1088763
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