4-Aryl-3-bromo-N-benzylmaleimides and 3,4-biaryl-N-benzylmaleimides have been synthesized by a modified Suzuki cross-coupling reaction from 3,4-dibromo-N-benzylmaleimide. The conformational studies by dynamic NMR and DFT calculations showed that the interconversion barrier between the two available skewed conformations is under steric control. When the aryl group was a 2-methylnaphthyl, thermally stable atropisomers were isolated by enantioselective HPLC and their absolute configurations were assigned by TD-DFT simulations of the ECD spectra.

Atropisomers of arylmaleimides: Stereodynamics and absolute configuration / M. Ambrogi; A. Ciogli; M. Mancinelli; S. Ranieri; A. Mazzanti. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - STAMPA. - 78:8(2013), pp. 3709-3719. [10.1021/jo400200v]

Atropisomers of arylmaleimides: Stereodynamics and absolute configuration

MANCINELLI, MICHELE;RANIERI, SILVIA;MAZZANTI, ANDREA
2013

Abstract

4-Aryl-3-bromo-N-benzylmaleimides and 3,4-biaryl-N-benzylmaleimides have been synthesized by a modified Suzuki cross-coupling reaction from 3,4-dibromo-N-benzylmaleimide. The conformational studies by dynamic NMR and DFT calculations showed that the interconversion barrier between the two available skewed conformations is under steric control. When the aryl group was a 2-methylnaphthyl, thermally stable atropisomers were isolated by enantioselective HPLC and their absolute configurations were assigned by TD-DFT simulations of the ECD spectra.
2013
Atropisomers of arylmaleimides: Stereodynamics and absolute configuration / M. Ambrogi; A. Ciogli; M. Mancinelli; S. Ranieri; A. Mazzanti. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - STAMPA. - 78:8(2013), pp. 3709-3719. [10.1021/jo400200v]
M. Ambrogi; A. Ciogli; M. Mancinelli; S. Ranieri; A. Mazzanti
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/151551
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