Highly Enantioselective Reformatsky Reaction of Ketones:  Chelation-Assisted Enantioface Discrimination

Akio Ojida, Toru Yamano, Naohiro Taya, Akihiro Tasaka

Organic Letters · 2002 · 53 citations · 15 references

Concepts

Abstract

[reaction: see text] Highly enantioselective Reformatsky reaction of ketones was accomplished using cinchona alkaloids as chiral ligands. Chelation with the sp(2)-nitrogen adjacent to the reactive carbonyl center contributed the enantioface discrimination for the high enantioselectivities.

References

15