A convenient method of protection and mild deprotection of α-aminoacid group for the synthesis of functional α-aminoacids

Article abstract of DOI:10.1080/00397919308018603

Functionalisation of β or γ carboxyl group of aspartic and glutamic acids with labile substituents was performed via the use of N-trichloroethoxycarbonyl-5-oxazolidinone as protective group.

Full text of DOI:10.1080/00397919308018603

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Synthetic Communications: An
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A Convenient Method of Protection
and Mild Deprotection of α-
Aminoacids
Jean-François Chollet a , Léone Miginiac a , Jérôme Rudelle b
& Jean-Louis Bonnemain b
a Laboratoire de Synthèse Organique, URA 574 CNRS ,
Université de Poitiers , 40, avenue du Recteur Pineau,
86022, Poitiers, France
b Laboratoire de Biochimie et Physiologie Végétales URA
574 CNRS , Université de Poitiers , 25 rue du Faubourg St
Cyprien 86000, Poitiers, France
Published online: 23 Sep 2006.
To cite this article: Jean-François Chollet , Léone Miginiac , Jérôme Rudelle & Jean-Louis
Bonnemain (1993) A Convenient Method of Protection and Mild Deprotection of α-Aminoacids,
Synthetic Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 23:15, 2101-2111, DOI: 10.1080/00397919308018603
To link to this article: http://dx.doi.org/10.1080/00397919308018603
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