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Enantioselective Formation of All‐Carbon Quaternary Stereocenters from Indoles and Tertiary Alcohols Bearing A Directing Group

80

Citations

63

References

2014

Year

Abstract

Abstract Described is an efficient catalytic asymmetric intermolecular CC bond‐formation process to generate acyclic all‐carbon quaternary stereocenters. The reactions overcome the unfavorable steric hindrance around reactive centers, and the competitive elimination (E1), to form a range of useful indole products with excellent efficiency and enantioselectivity.

References

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