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This article is cited in 14 scientific papers (total in 14 papers)
Ylides from dihalocarbenes and esters of N-benzhydrylidene amino acids: halogen-dependent reaction pathways
A. F. Khlebnikov, M. S. Novikov, R. R. Kostikov
Department of Chemistry, St. Petersburg State University, St. Petersburg, Russian Federation
Abstract:
The nature of the halogen dramatically affects the properties of azomethine ylides derived from dihalocarbenes and the benzophenone Schiff bases of amino acid esters: dichloro- and chlorofluoroylides cyclise to give gem-dihaloaziridines 2a–e, while difluoroylides characteristically undergo ylide–ylide isomerisation and 1,3-dipolar cycloaddition.
Citation:
A. F. Khlebnikov, M. S. Novikov, R. R. Kostikov, “Ylides from dihalocarbenes and esters of N-benzhydrylidene amino acids: halogen-dependent reaction pathways”, Mendeleev Commun., 7:4 (1997), 145–147
Linking options:
https://www.mathnet.ru/eng/mendc4827 https://www.mathnet.ru/eng/mendc/v7/i4/p145
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