A Robust, Efficient, and Highly Enantioselective Method for Synthesis of Homopropargyl Amines

Erika M. Vieira, Marc L. Snapper, Amir H. Hoveyda

Angewandte Chemie International Edition · 2012 · 67 citations · 31 references

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Abstract

Fast, robust, selective: Copper-catalyzed enantioselective additions of homopropargyl groups to a wide range of aldimines proceed readily and with high enantioselectivity. The catalytic method is scalable and practical, the allenylboron reagent is commercially available, and conversion into amines is inexpensive and high-yielding. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

References

31