A Highly Stereoselective Aza-[3,3]-Claisen Rearrangement of Vinylaziridines as a Novel Entry to Seven-Membered Lactams

Ulf M. Lindström; Peter Somfai

doi:10.1021/ja971572v

journal article Sep 01, 1997

A Highly Stereoselective Aza-[3,3]-Claisen Rearrangement of Vinylaziridines as a Novel Entry to Seven-Membered Lactams

Ulf M. Lindström Peter Somfai

Journal of the American Chemical Society Vol. 119 No. 35 pp. 8385-8386 · American Chemical Society (ACS)

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Compounds

Metrics

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Citations

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References

Details

Published: Sep 01, 1997
Vol/Issue: 119(35)
Pages: 8385-8386

Authors

U

Ulf M. Lindström

Organic Chemistry 2, Center for Chemistry and Chemical Engineering, Lund Institute of Technology Lund University, P.O. Box 124, S-221 00 Lund, Sweden

P

Peter Somfai

Organic Chemistry 2, Center for Chemistry and Chemical Engineering, Lund Institute of Technology Lund University, P.O. Box 124, S-221 00 Lund, Sweden

Cite This Article

Ulf M. Lindström, Peter Somfai (1997). A Highly Stereoselective Aza-[3,3]-Claisen Rearrangement of Vinylaziridines as a Novel Entry to Seven-Membered Lactams. Journal of the American Chemical Society, 119(35), 8385-8386. https://doi.org/10.1021/ja971572v

A Highly Stereoselective Aza-[3,3]-Claisen Rearrangement of Vinylaziridines as a Novel Entry to Seven-Membered Lactams

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