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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Article Doi

Regiospecific Palladium-Catalyzed Cycloaddition of Aziridines and Carbodiimides

DOI: 10.1021/jo00027a030

Source and publish data:

Authors:

Article abstract of DOI:10.1021/jo00027a030

Full text of DOI:10.1021/jo00027a030

Products guided by the article

R&D Labs maybe for 136912-62-4

Relevant to this article

Combinatorial aid for underprivileged scaffolds: Solution and solid-phase strategies for a rapid and efficient access to novel aza-diketopiperazines (aza-DKP)

A convenient and mild chromatography-free method for the purification of the products of Wittig and Appel reactions

Synthesis and bioactivity of substituted benzoylguanidine derivatives as potent Na+/H+ exchanger inhibitors

Syntheses and X-ray crystal structures of cassiferaldehyde and analogs

Dendrimeric amide- and carbamate-linked lysine-based efficient molecular transporters

Direct palladium(II)-catalyzed synthesis of arylamidines from aryltrifluoroborates

Synthesis and bioactivity of substituted benzoylguanidine derivatives as potent Na⁺/H⁺ exchanger inhibitors