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- W2103961844 endingPage "2964" @default.
- W2103961844 startingPage "2960" @default.
- W2103961844 abstract "Taking the Michael: The first highly enantio- and diastereoselective Michael addition of various 3-benzyl-substituted oxindoles to 2-cyclopentenone has been developed. A variety of 3,3-disubstituted oxindoles as Michael adducts were obtained in 69–99 % yield with 73–98 % ee and 9:1 to >20:1 d.r. 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.
- W2103961844 created "2016-06-24" @default.
- W2103961844 creator A5017162812 @default.
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- W2103961844 creator A5066240016 @default.
- W2103961844 creator A5069352060 @default.
- W2103961844 creator A5076289876 @default.
- W2103961844 date "2013-09-20" @default.
- W2103961844 modified "2023-10-07" @default.
- W2103961844 title "Bicyclic-Guanidine-Catalyzed Asymmetric Michael Addition of 3-Substituted Oxindoles to 2-Cyclopentenone" @default.
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