Stereoselective synthesis of 4-amino-3-hydroxy-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole-4-carboxylic acid, a conformationally constrained analogue of aspartic acid
Articolo
Data di Pubblicazione:
2007
Citazione:
Stereoselective synthesis of 4-amino-3-hydroxy-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole-4-carboxylic acid, a conformationally constrained analogue of aspartic acid / P. Conti, A. Pinto, G. Roda, L. Tamborini, D. Arosio, C. De Micheli. - In: SYNTHESIS. - ISSN 0039-7881. - 14:14(2007 Jul 17), pp. 2145-2148. [10.1055/s-2007-983750]
Abstract:
An alternative synthesis of 4-amino-3-hydroxy-4,5,6,6a-tetrahydro-3aH- cyclopenta[d]isoxazole-4-carboxylic acid, a conformationally constrained analogue of aspartic acid, is described. The synthetic strategy is based on a regioselective 1,3-dipolar cycloaddition to give the cyclopenta[d]isoxazoline framework; subsequent condensation of this 4-oxocyclopenta[d]isoxazoline with 4-methoxybenzylamine gives a 4-imino derivative, which undergoes a highly stereoselective nucleophilic attack by the cyanide ion. This gives a 4-(methoxybenzylamino)-4-cyano derivative, which is oxidized to the corresponding 4-amino-4-cyano derivative, which itself is transformed into the target 4-carboxylic acid. This amino acid is obtained in 27% overall yield in five steps, whereas the previously described synthetic strategy gave the target derivative in only 0.5% overall yield over 15 steps.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
1,3-dipolar cycloaddition; Aspartate analogues; Glutamate transporters; Heterocycles; Stereoselective synthesis;
Elenco autori:
P. Conti, A. Pinto, G. Roda, L. Tamborini, D. Arosio, C. De Micheli
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