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Volumn 55, Issue 18, 1999, Pages 5681-5704

Rotational features of carbon-nitrogen bonds in N-aryl maleimides. Atroposelective reactions of o-tert-butylphenylmaleimides

Author keywords

Amides; Atroposelectivity; Axial chirality; Rotation barrier

Indexed keywords

MALEIMIDE DERIVATIVE; N2 (TERT BUTYLPHENYL)MALEIMIDE; N2,5 DI(TERT BUTYLPHENYL)MALEIMIDE; UNCLASSIFIED DRUG;

EID: 0033617110     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00237-9     Document Type: Article
Times cited : (83)

References (42)
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    • The unselective nitrile oxide cycloadditions to axially chiral N-aryl maleimides in the following paper
    • 14. For example, see the unselective nitrile oxide cycloadditions to axially chiral N-aryl maleimides in the following paper: Konopikova, M.; Fisera, L.; Goljer, I; Varkonda, S.; Hyblova, O.; Sturdik, E.; Ujhelyova, R. Chem. Pap. 1991, 45, 789; Chem. Abstr. 1992, 116, 151622u.
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    • 151622u
    • 14. For example, see the unselective nitrile oxide cycloadditions to axially chiral N-aryl maleimides in the following paper: Konopikova, M.; Fisera, L.; Goljer, I; Varkonda, S.; Hyblova, O.; Sturdik, E.; Ujhelyova, R. Chem. Pap. 1991, 45, 789; Chem. Abstr. 1992, 116, 151622u.
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