Enantiomerically pure 1,4-dihydropyridines are prepared taking advantage of magnesium nitride as a useful and convenient source of 'solid ammonia'. The products possess various substituents at carbons 3, 4 and 5 of the dihydropyridine moiety.

The Use of Magnesium Nitride for the Synthesis of Enantiomerically Pure 1,4-Dihydropyridines via the Hantzsch Reaction

Panunzio M;
2011-01-01

Abstract

Enantiomerically pure 1,4-dihydropyridines are prepared taking advantage of magnesium nitride as a useful and convenient source of 'solid ammonia'. The products possess various substituents at carbons 3, 4 and 5 of the dihydropyridine moiety.
2011
Istituto per la Sintesi Organica e la Fotoreattivita' - ISOF
CHANNEL ANTAGONIST ACTIVITY; CONVENIENT SOURCE; TRANSFER HYDROGENATION; 1
4-DIHYDROPYRIDINE-3
5-DICARBOXYLATES; AMMONIA; LIPASE; DIHYDROPYRIDINES; DERIVATIVES; IMINES
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/234848
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