The stereoselective synthesis of highly functionalized 1,2,3-trisubstituted cyclopropanes 1 and 2, starting from readily available furans 3 or N-protected pyrrole 4, is described. Furthermore, exceptionally high diastereocontrol in agreement with the Felkin-Anh model was observed for the addition of nucleophiles to the title compounds.

Bohm C., Schinnerl M., Bubert C., Zabel M., Labahn T., Parisini E., et al. (2000). A new strategy for the stereoselective synthesis of 1,2,3-trisubstituted cyclopropanes. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2000(16), 2955-2965 [10.1002/1099-0690(200008)2000:16<2955::AID-EJOC2955>3.0.CO;2-3].

A new strategy for the stereoselective synthesis of 1,2,3-trisubstituted cyclopropanes

Parisini E.;
2000

Abstract

The stereoselective synthesis of highly functionalized 1,2,3-trisubstituted cyclopropanes 1 and 2, starting from readily available furans 3 or N-protected pyrrole 4, is described. Furthermore, exceptionally high diastereocontrol in agreement with the Felkin-Anh model was observed for the addition of nucleophiles to the title compounds.
2000
Bohm C., Schinnerl M., Bubert C., Zabel M., Labahn T., Parisini E., et al. (2000). A new strategy for the stereoselective synthesis of 1,2,3-trisubstituted cyclopropanes. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2000(16), 2955-2965 [10.1002/1099-0690(200008)2000:16<2955::AID-EJOC2955>3.0.CO;2-3].
Bohm C.; Schinnerl M.; Bubert C.; Zabel M.; Labahn T.; Parisini E.; Reiser O.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/916190
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