cheminform abstract: broensted acid-promoted aziridination of electron-deficient olefins

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ChemInform 2009, 40, issue 16 © 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Aziridine derivatives R 0040 Broensted Acid-Promoted Aziridination of Electron-Deficient Olefins. — The re- action mechanism is systematically studied using a combined theoretical and experi- mental approach. The efficiency of this reaction is shown to strongly depend on the ba- sicity of the olefins used. Accordingly, TfOH readily promotes the aziridination of var- ious acrylamides (I), while less basic acrylates and acrylonitrile are significantly less reactive. — (LI, J.; FU*, Y.; GUO, Q.-X.; Tetrahedron 64 (2008) 49, 11167-11174; Dep. Chem., Univ. Sci. Technol. China, Hefei 230026, Anhui, Peop. Rep. China; Eng.) — Mischke 16- 097

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Page 1: ChemInform Abstract: Broensted Acid-Promoted Aziridination of Electron-Deficient Olefins

www.cheminform.wiley-vch.de

Aziridine derivativesR 0040 Broensted Acid-Promoted Aziridination of Electron-Deficient Olefins. — The re-

action mechanism is systematically studied using a combined theoretical and experi-mental approach. The efficiency of this reaction is shown to strongly depend on the ba-sicity of the olefins used. Accordingly, TfOH readily promotes the aziridination of var-ious acrylamides (I), while less basic acrylates and acrylonitrile are significantly less reactive. — (LI, J.; FU*, Y.; GUO, Q.-X.; Tetrahedron 64 (2008) 49, 11167-11174; Dep. Chem., Univ. Sci. Technol. China, Hefei 230026, Anhui, Peop. Rep. China; Eng.) — Mischke

16- 097

ChemInform 2009, 40, issue 16 © 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim