Amide Group Directed Protonolysis of Cyclopropane. En Route To 2,2-Disubstituted Pyrrolidines

Marija Skvorcova; Aigars Jirgensons

Amide Group Directed Protonolysis of Cyclopropane. En Route To 2,2-Disubstituted Pyrrolidines

Latvijas Universitātes 75.Starptautiskā konference. Ķīmijas sekcija: tēžu krājums 2017
Marija Skvorcova, Aigars Jirgensons

We have demonstrated that cyclopropanes with amide, carbamate or urea function can selectively direct the proton attack to cyclopropane C-C bond, while in the case of electron withdrawing amide the cleavage was unselective. We have explored substrate scope for the transformation of aminomethylcyclopropanes to pyrrolidines using carbamate function as a directing group.

Atslēgas vārdi
carbamate, protonolysis, cyclopropane, pyrrolidine

Skvorcova, M., Jirgensons, A. Amide Group Directed Protonolysis of Cyclopropane. En Route To 2,2-Disubstituted Pyrrolidines. No: Latvijas Universitātes 75.Starptautiskā konference. Ķīmijas sekcija: tēžu krājums, Latvija, Rīga, 10.-10. februāris, 2017. Rīga: Latvijas Universitāte, 2017, 24.-24.lpp. ISBN 978-9934-18-206-8.

Publikācijas valoda
English (en)