Artículo
Stereoselective synthesis of chiral furan amino acid analogues of D- and L-serine from D-sugars
Autor/es | Molina, Lidia
Moreno Vargas, Antonio José Carmona Asenjo, Ana Teresa Robina Ramírez, Inmaculada |
Departamento | Universidad de Sevilla. Departamento de Química orgánica |
Fecha de publicación | 2006 |
Fecha de depósito | 2017-07-27 |
Publicado en |
|
Resumen | The synthesis of chiral furan amino acid analogues of
D
-
and
L
-serine is reported. The developed methodology starting from
D
-xylose affords the corresponding amino acid derivative analogue
of
D
-serine ... The synthesis of chiral furan amino acid analogues of D - and L -serine is reported. The developed methodology starting from D -xylose affords the corresponding amino acid derivative analogue of D -serine enantiomerically pure. Starting from D -arabinose, the corresponding analogue of L -serine was isolated in 92.3% enantio- meric purity. The analogue of D -serine was transformed into a stable Fmoc activated derivative ready to be incorporated into peptides. |
Identificador del proyecto | CTQ2004-00649/BQU
FP6 TRIoH info:eu-repo/grantAgreement/EC/FP6/503480 FQM-345 |
Cita | Molina, L., Moreno Vargas, A.J., Carmona Asenjo, A.T. y Robina Ramírez, I. (2006). Stereoselective synthesis of chiral furan amino acid analogues of D- and L-serine from D-sugars. Synlett, 9, 1327-1330. |
Ficheros | Tamaño | Formato | Ver | Descripción |
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Stereoselective Synthesis.pdf | 80.41Kb | [PDF] | Ver/ | |