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• W2003067996 abstract "The multitalented catalyst 1/Ni(ClO4)2 mediates both title processes (see scheme). Together the efficient asymmetric cycloaddition and a kinetic resolution/cycloaddition provide access to both enantiomers of tetrahydro-1,2-oxazines. DME=1,2-dimethoxyethane; R1=aryl, vinyl; R2=Et, Me, benzyl; R3=Me, Ph; R4=aryl, styryl. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2007/z604645_s.pdf or from the author. 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.
• W2003067996 created "2016-06-24" @default.
• W2003067996 creator A5051560553 @default.
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• W2003067996 date "2007-05-15" @default.
• W2003067996 modified "2023-10-17" @default.
• W2003067996 title "Highly Enantioselective and Diastereoselective Cycloaddition of Cyclopropanes with Nitrones and Its Application in the Kinetic Resolution of 2-Substituted Cyclopropane-1,1-dicarboxylates" @default.
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• W2003067996 doi "https://doi.org/10.1002/anie.200604645" @default.
• W2003067996 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17437309" @default.
• W2003067996 hasPublicationYear "2007" @default.
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