83427-81-0Relevant articles and documents
Model studies towards the applicability of the readily available (S)-N-tritylaspartic anhydride in the synthesis of amino acids and peptides
Athanassopoulos,Athanassopoulos, Constantinos,Tzavara,Tzavara, Chryssoula,Papaioannou,Papaioannou, Dionissios,Sindona,Sindona, Giovanni,Maia,Maia, Hernani L. S.
, p. 2679 - 2688 (2007/10/02)
Reactions of N-tritylaspartic acid anhydride, readily available through N,N'-dicyclo-hexylcarbodiimide-mediated dehydration of N-tritylaspartic acid, with Grignard and Wittig reagents, bulky hydrides, and amines or alcohols of the benzhydryl type, lead regioselectively to products from attack at the β-carbonyl function.
Synthesis and rearrangement of homoserine derivatives
Baldwin,North,Flinn
, p. 637 - 642 (2007/10/02)
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L-Canaline Derivatives of Interest in Peptide Synthesis
Barlos, Kleomenis,Papaioannou, Dionysios,Sanida, Chariklia
, p. 287 - 291 (2007/10/02)
(S)-4-(tert-Butyloxycarbonylaminooxy)-2-(tritylamino)butyric acid (8) and the p-toluenesulfonate of phenacyl (S)-2-amino-4-(phthalimidooxy)butyrate (10) have been synthesized from N-tritylhomoserine (2) in five and three steps, respectively.