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Preparation and ring-opening reactions of N-diphenylphosphinyl vinyl aziridines

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Jarvis, A. N., McClaren, A. B., Osborn, H. M. I. orcid id iconORCID: https://orcid.org/0000-0002-0683-0457 and Sweeney, J. (2013) Preparation and ring-opening reactions of N-diphenylphosphinyl vinyl aziridines. Beilstein Journal of Organic Chemistry, 9. pp. 852-859. ISSN 1860-5397 doi: 10.3762/bjoc.9.98

Abstract/Summary

Predominantly (E)-N-diphenylphosphinyl vinyl aziridines are prepared by a reaction of N-diphenylphosphinyl imines with α-bromoallyllithium in the presence of freshly fused ZnCl2. These aziridines undergo a ring-opening reaction with a variety of carbon and heteronucleophiles, in good yield, and generally with good regioselectivity.

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Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/32479
Identification Number/DOI 10.3762/bjoc.9.98
Refereed Yes
Divisions Life Sciences > School of Chemistry, Food and Pharmacy > School of Pharmacy > Medicinal Chemistry Research Group
Publisher Beilstein-Institut
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