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• W2133295053 endingPage "8815" @default.
• W2133295053 startingPage "8811" @default.
• W2133295053 abstract "Spiro compounds: An organocatalytic asymmetric method for the CH functionalization of the α position of racemic cyclic ethers has been developed. The transformation, mediated by catalytic amounts of an imidazolidinone and strong acid, involves a tandem 1,5-hydride transfer/cyclization and provides access to a structurally diverse series of chiral spiroethers with high levels of enantioselectivity (see scheme). 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.
• W2133295053 created "2016-06-24" @default.
• W2133295053 creator A5008346135 @default.
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• W2133295053 creator A5067879579 @default.
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• W2133295053 date "2012-07-31" @default.
• W2133295053 modified "2023-10-18" @default.
• W2133295053 title "Organocatalytic Asymmetric Direct C sp 3H Functionalization of Ethers: A Highly Efficient Approach to Chiral Spiroethers" @default.
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