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• W2119648415 endingPage "6316" @default.
• W2119648415 startingPage "6313" @default.
• W2119648415 abstract "Oxindoles with a twist: Transfer hydrogenation of substituted isatins in the presence of allyl acetate, α-methyl allyl acetate, or 1,1,-dimethylallene using an cyclometalated iridium catalyst, provides products of carbonyl allylation, crotylation, and reverse prenylation, respectively, in highly enantiomerically enriched form. These studies represent the first use of activated ketones as electrophilic partners in asymmetric CC bond-forming transfer hydrogenation. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by 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.
• W2119648415 created "2016-06-24" @default.
• W2119648415 creator A5006111382 @default.
• W2119648415 creator A5022217449 @default.
• W2119648415 creator A5042928999 @default.
• W2119648415 date "2009-07-15" @default.
• W2119648415 modified "2023-09-27" @default.
• W2119648415 title "Enantioselective Allylation, Crotylation, and Reverse Prenylation of Substituted Isatins: Iridium-Catalyzed CC Bond-Forming Transfer Hydrogenation" @default.
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• W2119648415 doi "https://doi.org/10.1002/anie.200902328" @default.
• W2119648415 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2846777" @default.
• W2119648415 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19606435" @default.
• W2119648415 hasPublicationYear "2009" @default.
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