Lewis Acid Promoted Highly Stereoselective Rearrangement of 2,3-Aziridino Alcohols:  A New Efficient Approach to β-Amino Carbonyl Compounds

Bao Min Wang, Zhen Lei Song, Chun‐An Fan, Yong Qiang Tu, Yian Shi

Organic Letters · 2002 · 38 citations · 17 references

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Abstract

A new Lewis acid promoted rearrangement reaction of 2,3-aziridino alcohols was discovered, which involved the highly stereoselective construction of a diastereogenic quaternary carbon center and efficient formation of beta-amino carbonyl compounds in excellent yields. A wide variety of Lewis acids were proved to be effective for the reaction, and a possible reaction mechanism was also discussed.

References

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