Starting from a suitably functionalized aziridine, a highly efficient stereoselective synthesis of (1R,2R)-phenyl-2-decanoylamino- 3-morpholinopropan-1-ol (D-threo-PDMP) is described. The approach, based on the ring expansion of the aziridine ring to oxazoline, could be applicable to the synthesis of many analogues with different amide chains and sugar mimic portions.
New Highly Efficient Stereoselective Synthesis of d-threo-PDMP / Giuliana, R., Paolo, B., Francesca, M., Federica, M., Mandic', E., Pelagalli, R.. - In: SYNTHESIS. - ISSN 0039-7881. - STAMPA. - 2011:20(2011), pp. 3318-3322. [10.1055/s-0030-1260225]
New Highly Efficient Stereoselective Synthesis of d-threo-PDMP
MANDIC', EMANUELA;PELAGALLI, ROMINA
2011
Abstract
Starting from a suitably functionalized aziridine, a highly efficient stereoselective synthesis of (1R,2R)-phenyl-2-decanoylamino- 3-morpholinopropan-1-ol (D-threo-PDMP) is described. The approach, based on the ring expansion of the aziridine ring to oxazoline, could be applicable to the synthesis of many analogues with different amide chains and sugar mimic portions.File allegati a questo prodotto
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