Synthesis of (R)-dihydropyridones as key intermediates for an efficient access to piperidine alkaloids

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Abstract

The efficient transformation of D-glucal to (2R)- hydroxymethyldihydropyridinone 5 in seven steps and 35 % overall yield is reported. Dihydropyridone 5 constitutes a versatile chiral building block for the synthesis of various piperidine alkaloids. In this regard, 5 was converted to piperidinol 13 and piperidinone 15, that may be further elaborated for the syntheses of (+)-desoxoprosophylline (1) and deoxymannojirimycin (3) or D-mannolactam (4), respectively. © 2007 by MDPI.

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Tzanetou, E. N., Kasiotis, K. M., Magiatis, P., & Haroutounian, S. A. (2007). Synthesis of (R)-dihydropyridones as key intermediates for an efficient access to piperidine alkaloids. Molecules, 12(4), 735–744. https://doi.org/10.3390/12040735

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