January 1, 2012Chemical Communications

Enantioselective aza-Henry reactions of cyclic α-carbonyl ketimines under bifunctional catalysis

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Abstract

The aza-Henry reaction of nitroalkanes with the C=N group of 2-aryl-3H-indol-3-ones catalyzed by thiourea-chincona derivatives takes place with good yield and high ee's.

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Parra et al. (2012) studied this question.

synapsesocial.com/papers/69fcea36015782f43c50916b https://doi.org/10.1039/c2cc34053d

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Abstract

The aza-Henry reaction of nitroalkanes with the C=N group of 2-aryl-3H-indol-3-ones catalyzed by thiourea-chincona derivatives takes place with good yield and high ee's.

Enantioselective aza-Henry reactions of cyclic α-carbonyl ketimines under bifunctional catalysis

Abstract

Discussion

Cite This Study

Enantioselective aza-Henry reactions of cyclic α-carbonyl ketimines under bifunctional catalysis

Abstract

Discussion

Cite This Study

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