The synthesis of new substituted prolines carrying at C-4 a second α-amino acid residue is reported. The amino acid, l-cysteine or l-selenocysteine, is linked to the proline ring through the sulfur or the selenium atom, respectively. The products were prepared with different stereochemistry at C-4, in few and clean high-yielding steps, with suitable protections for solid phase applications. The introduction of both sulfur and selenium atoms at C-4 of the proline ring seems to enhance significantly the cis geometry at the prolyl amide bond.
Novel sulfur and selenium containing bis-α-amino acids from 4-hydroxyproline / Caputo, Romualdo; DELLA GRECA, Marina; I., de PAOLA; D., Mastroianni; Longobardo, Luigi. - In: AMINO ACIDS. - ISSN 0939-4451. - STAMPA. - 38:1(2010), pp. 305-310. [10.1007/s00726-009-0251-x]
Novel sulfur and selenium containing bis-α-amino acids from 4-hydroxyproline
CAPUTO, ROMUALDO;DELLA GRECA, MARINA;LONGOBARDO, LUIGI
2010
Abstract
The synthesis of new substituted prolines carrying at C-4 a second α-amino acid residue is reported. The amino acid, l-cysteine or l-selenocysteine, is linked to the proline ring through the sulfur or the selenium atom, respectively. The products were prepared with different stereochemistry at C-4, in few and clean high-yielding steps, with suitable protections for solid phase applications. The introduction of both sulfur and selenium atoms at C-4 of the proline ring seems to enhance significantly the cis geometry at the prolyl amide bond.File | Dimensione | Formato | |
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