An Efficient One-Pot Conversion of Alkyl Bromides into Imines via the Staudinger Reaction

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Authors	VANĚK Petr KLÁN Petr
Year of publication	2000
Type	Article in Periodical
Magazine / Source	Synthetic Communications
MU Faculty or unit	Faculty of Science
Citation
Field	Organic chemistry
Keywords	photochemistry
Description	A new one-pot procedure for transforming primary alkyl bromides into the corresponding imines via the Staudinger reaction has been developed. Acetonitrile was found to be an excellent solvent for azidation as well as the reaction of organic azide with triphenylphosphine and a carbonyl compound.
Related projects:	Structure and character of bonding, properties and analysis of synthetic and natural molecular ensembles