In search for novel conformationally constrained analogues of L-glutamic acid, a diastereodivergent synthesis of the four 1-aminospiro[2.2]pentyl-1,4-dicarboxylic acid racemic pairs is reported along with their stereochemical assignment, conformational analysis, and preliminary biological evaluation as potential glutamate (ionotropic and metabotropic) ligands.

Pellicciari, R.a.S.m.t.P.R., Marinozzi, M.a., Camaioni, E., Nùnez, M.d.C., Costantino, G., Gasparini, F., et al. (2002). Spiro[2.2]Pentane as a Dissymmetric Scaffold for Conformationally Constrained Analogues of Glutamic Acid: Focus on Racemic 1-Aminospiro[2.2]pentyl-1,4-Dicarboxylic Acids. JOURNAL OF ORGANIC CHEMISTRY, 67(16), 5497-5507 [10.1021/jo020138v].

Spiro[2.2]Pentane as a Dissymmetric Scaffold for Conformationally Constrained Analogues of Glutamic Acid: Focus on Racemic 1-Aminospiro[2.2]pentyl-1,4-Dicarboxylic Acids

Giorgi, Gianluca;
2002-01-01

Abstract

In search for novel conformationally constrained analogues of L-glutamic acid, a diastereodivergent synthesis of the four 1-aminospiro[2.2]pentyl-1,4-dicarboxylic acid racemic pairs is reported along with their stereochemical assignment, conformational analysis, and preliminary biological evaluation as potential glutamate (ionotropic and metabotropic) ligands.
2002
Pellicciari, R.a.S.m.t.P.R., Marinozzi, M.a., Camaioni, E., Nùnez, M.d.C., Costantino, G., Gasparini, F., et al. (2002). Spiro[2.2]Pentane as a Dissymmetric Scaffold for Conformationally Constrained Analogues of Glutamic Acid: Focus on Racemic 1-Aminospiro[2.2]pentyl-1,4-Dicarboxylic Acids. JOURNAL OF ORGANIC CHEMISTRY, 67(16), 5497-5507 [10.1021/jo020138v].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/10100
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