Antibiotics and Antimycotics

2,6-Dichloro-3-nitropyridine undergoes macrocyclic condensation reaction with resorcinol derivatives to yield chiral tetraoxacalix[2]arene[2]pyridines.

2,6-Dichloro-3-nitropyridine undergoes macrocyclic condensation reaction with resorcinol derivatives to yield chiral tetraoxacalix[2]arene[2]pyridines.

Application:In order to synthesize macrocycles containing pyridine, 2,6-his-(bromomethyl)pyridine was prepared by bromonating 2,6-di (hydroxymethyl)pyridine.

Application:In order to synthesize macrocycles containing pyridine, 2,6-his-(bromomethyl)pyridine was prepared by bromonating 2,6-di (hydroxymethyl)pyridine.

2,6-Pyridinedicarbonitrile is a heterocyclic dinitrile. Its biotransformation by Rhodococcus erythropolis A4 to 6-cyanopyridine-2-carboxamide has been reported.

2,6-Pyridinedicarbonitrile is a heterocyclic dinitrile. Its biotransformation by Rhodococcus erythropolis A4 to 6-cyanopyridine-2-carboxamide has been reported.

2,6-Pyridinedicarbonitrile is a heterocyclic dinitrile. Its biotransformation by Rhodococcus erythropolis A4 to 6-cyanopyridine-2-carboxamide has been reported.

2,6-Pyridinedicarbonitrile is a heterocyclic dinitrile. Its biotransformation by Rhodococcus erythropolis A4 to 6-cyanopyridine-2-carboxamide has been reported.

2,6-Pyridinedicarbonitrile is a heterocyclic dinitrile. Its biotransformation by Rhodococcus erythropolis A4 to 6-cyanopyridine-2-carboxamide has been reported.

2,7-Di(1-pyrenyl)-9,9'-spirobi[9H-fluorene].

2,7-Di(1-pyrenyl)-9,9'-spirobi[9H-fluorene].

2,7-Di(1-pyrenyl)-9,9'-spirobi[9H-fluorene].