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- W2074429853 abstract "Taming the beast, asymmetrically: Modulation of the reactivity of acid chlorides, using cinchona alkaloid catalysts, results in chiral α,β-unsaturated acylammoniums, which react with nucleophiles enantioselectively to give pyrrolidinones, piperid-2-ones, and dihydropyridinones. This nucleophile-catalyzed Michael/proton transfer/lactamization or lactonization organocascade leads to chiral intermediates previously employed for the synthesis of bioactive pharmaceuticals. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
- W2074429853 created "2016-06-24" @default.
- W2074429853 creator A5011880323 @default.
- W2074429853 creator A5069520021 @default.
- W2074429853 creator A5034540054 @default.
- W2074429853 date "2013-10-31" @default.
- W2074429853 modified "2023-10-18" @default.
- W2074429853 title "Direct Catalytic Asymmetric Synthesis of N-Heterocycles from Commodity Acid Chlorides by Employing α,β-Unsaturated Acylammonium Salts" @default.
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- W2074429853 doi "https://doi.org/10.1002/anie.201306050" @default.
- W2074429853 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24173690" @default.
- W2074429853 hasPublicationYear "2013" @default.
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