A practical synthesis of N α -Fmoc protected l-threo-β-hydroxyaspartic acid derivatives for coupling via α- or β-carboxylic group-Reference-Cited by-同舟云学术

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A practical synthesis of N α -Fmoc protected l-threo-β-hydroxyaspartic acid derivatives for coupling via α- or β-carboxylic group

Published:2010-11-17 Issue:1 Volume:42 Page:285-293
ISSN:0939-4451
Container-title:Amino Acids
language:en
Short-container-title:Amino Acids

Author:

Bionda Nina,Cudic Maré,Barisic Lidija,Stawikowski Maciej,Stawikowska Roma,Binetti Diego,Cudic Predrag

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Clinical Biochemistry,Biochemistry

Link

http://link.springer.com/content/pdf/10.1007/s00726-010-0806-x.pdf

Reference55 articles.

1. Barbayianni E, Fotakopoulou I, Schmidt M, Constantinou-Kokotou V, Bornscheuer UT, Kokotos G (2005) Enzymatic removal of carboxyl protecting groups. 2. Cleavage of the benzyl and methyl moieties. J Org Chem 70:8730–8733

2. Berthelot T, Gonçalves M, Laïn G, Estieu-Gionnet K, Déléris G (2006) New strategy towards the efficient solid phase synthesis of cyclopeptides. Tetrahedron 62:1124–1130

3. Bhushan R, Brückner H (2004) Marfey’s reagent for chiral amino acid analysis: a review. Amino Acids 27:231–247

4. Boger DL, Lee RJ, Bounaud P-Y, Meier P (2000) Asymmetric synthesis of orthogonally protected l-threo-β-hydroxyasparagine. J Org Chem 65:6770–6772

5. Bommarius AS, Drauz K, Klenk H, Wandrey C (1992) Operational stability of enzymes: acylase-catalyzed resolution of N-acetyl amino acids to enantiomerically pure l-amino acids. Ann N Y Acad Sci 672:126–136

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