Regiospecific Palladium-Catalyzed Cycloaddition of Aziridines and Carbodiimides

DOI: 10.1021/jo00027a030

Source and publish data:

Journal of Organic Chemistry p. 157 - 162 (1992)

Update date:2022-07-29

Topics: Palladium Carbodiimides Cycloaddition Aziridines Regiospecific

Authors:

Baeg, Jin-Ook

Alper, Howard

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Article abstract of DOI:10.1021/jo00027a030

Bis(benzonitrile)palladium dichloride is an effective catalyst for the cycloaddition reaction of aziridines with carbodiimides to form imidazolidinimines in 40-94 percent yields.The process is a regiospecific one, involving cleavage of the more substitute

Full text of DOI:10.1021/jo00027a030

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