The efficient desymmetrization of N-(2-tert-butylphenyl)maleimides was realized by means of a Michael addition reaction of a series of carbon nucleophiles generating the corresponding axially chiral succinimides in high yields. The use of (DHQD)2Pyr as catalyst was fundamental to achieve the remote control of the stereogenic chiral axis with the concurrent construction of adjacent quaternary and tertiary stereocenters.

Di Iorio, N., Champavert, F., Erice, A., Righi, P., Mazzanti, A., Bencivenni, G. (2016). Targeting remote axial chirality control of N-(2-tert-butylphenyl)succinimides by means of Michael addition type reactions. TETRAHEDRON, 72, 5191-5201 [10.1016/j.tet.2016.02.052].

Targeting remote axial chirality control of N-(2-tert-butylphenyl)succinimides by means of Michael addition type reactions

DI IORIO, NICOLA;RIGHI, PAOLO;MAZZANTI, ANDREA;BENCIVENNI, GIORGIO
2016

Abstract

The efficient desymmetrization of N-(2-tert-butylphenyl)maleimides was realized by means of a Michael addition reaction of a series of carbon nucleophiles generating the corresponding axially chiral succinimides in high yields. The use of (DHQD)2Pyr as catalyst was fundamental to achieve the remote control of the stereogenic chiral axis with the concurrent construction of adjacent quaternary and tertiary stereocenters.
2016
Di Iorio, N., Champavert, F., Erice, A., Righi, P., Mazzanti, A., Bencivenni, G. (2016). Targeting remote axial chirality control of N-(2-tert-butylphenyl)succinimides by means of Michael addition type reactions. TETRAHEDRON, 72, 5191-5201 [10.1016/j.tet.2016.02.052].
Di Iorio, Nicola; Champavert, Florian; Erice, Agostino; Righi, Paolo; Mazzanti, Andrea; Bencivenni, Giorgio
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/565512
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