2017
DOI: 10.1002/cctc.201601530
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“Side‐Product Catalysis”: Substrate Autoxidation as an Overlooked Side Reaction Generating a Co‐Catalyst for Enhancing Asymmetric Aldol Reactions

Abstract: An acid formed autoxidatively from an aldehyde substrate as a side product was found to alter the reaction kinetics and selectivity significantly in the direct asymmetric aldol reaction between an aldehyde and acetone, both in aqueous media and cyclohexane. Furthermore, this side‐product catalysis (“impurity catalysis”) was also observed upon using commercial samples of aldehydes without purification prior to their use (owing to the presence of the acid formed therein during storage), which thus underlines the… Show more

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Cited by 6 publications
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“…The following supporting information can be downloaded at https: //www.mdpi.com/article/10.3390/catal12040433/s1, Figure S1 S1: DLS analysis of 13a and SC5II with or without coordinated copper; Table S2: Elemental analysis of strains 13a and SC5II with or without Cu(II) or Cu(I) coordinated. References [18,38,44,45] are cited in the Supplementary Materials. Funding: The research and APC were supported by Fondazione CARIPLO-Circular Economy 2020 project num.…”
Section: Supplementary Materialsmentioning
confidence: 99%
“…The following supporting information can be downloaded at https: //www.mdpi.com/article/10.3390/catal12040433/s1, Figure S1 S1: DLS analysis of 13a and SC5II with or without coordinated copper; Table S2: Elemental analysis of strains 13a and SC5II with or without Cu(II) or Cu(I) coordinated. References [18,38,44,45] are cited in the Supplementary Materials. Funding: The research and APC were supported by Fondazione CARIPLO-Circular Economy 2020 project num.…”
Section: Supplementary Materialsmentioning
confidence: 99%