Journal
ORGANIC LETTERS
Volume 21, Issue 9, Pages 3013-3017Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b00505
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Funding
- University of Bologna
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The organocatalytic axially enantioselective Knoevenagel condensation between prochiral cyclohexanones and oxindoles is presented. The reaction, promoted by a primary amine, proceeded smoothly and furnished unprecedented examples of novel cyclohexylidene oxindoles displaying axial chirality.
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