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DOI: 10.1055/s-2007-983759
[2+2] Photocycloadditions with Chiral Uracil Derivatives: Access to All Four Stereoisomers of 2-Aminocyclobutanecarboxylic Acid
Publication History
Publication Date:
03 July 2007 (online)
Abstract
Starting from a single, chiral, bicyclic derivative of uracil, all four stereoisomers of 2-aminocyclobutanecarboxylic acid have been prepared in enantiomerically pure form, using a synthetic sequence which begins with a key photochemical [2+2] cycloaddition reaction and includes a practical cis to trans β-amino acid isomerisation procedure.
Key words
photochemistry - heterocycles - β-amino acids - cyclobutanes - stereoselective synthesis
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References
Crystallographic data for (-)-13a: C14H14N2O2, M = 242.27, T = 293 K, space group P61, a = 8.3788 (4) Å, b = 8.3788 (4) Å, c = 28.4565 (17) Å, α = 90.00°, β = 90.00°, γ = 120.00°, Z = 6, V = 1730.12 (16) Å3, ρcalcd = 1.395 g/cm-3. Full crystallographic data have been deposited with the Cambridge Crystallographic Data Centre (CCDC) as supplementary publication number CCDC 626949. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge, CB2 1EZ, UK, fax: +44(1223)336033, e-mail: deposit@ccdc.cam.ac.uk.