New, General, and Practical Enamine Cyclopropanation Using Dichloromethane

Chia‐Chung Tsai, I‐Lin Hsieh, Tsung‐Ting Cheng, Ping‐Kuei Tsai, Kuo‐Wei Lin, Tu‐Hsin Yan

Organic Letters · 2006 · 40 citations · 23 references

Concepts

Abstract

[reaction: see text] Dichloromethane serves as a novel electrophilic carbene equivalent which adds to an enamine double bond. The presence of other alkene moieties in the enamine partner is well tolerated. Even enamines derived from sterically hindered ketones react readily with dichloromethane promoted by TiCl(4)-Mg.

References

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