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• W2110366390 abstract "Ring in the new: A new annulation for the efficient synthesis of substituted furans and pyrroles is reported. The RhIII-catalyzed reaction of O-methyl α,β-unsaturated oximes with aldehydes and N-tosyl imines affords secondary alcohol and amine intermediates, respectively. Cyclization and aromatization occurs under the reaction conditions to provide access to biologically relevant furans and pyrroles in good yields. Cp*=C5Me5, DCE=1,2-dichloroethane, THF=tetrahydrofuran. 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.
• W2110366390 created "2016-06-24" @default.
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• W2110366390 date "2012-11-22" @default.
• W2110366390 modified "2023-10-06" @default.
• W2110366390 title "Rhodium(III)-Catalyzed Alkenyl CH Bond Functionalization: Convergent Synthesis of Furans and Pyrroles" @default.
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• W2110366390 doi "https://doi.org/10.1002/anie.201207995" @default.
• W2110366390 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3770945" @default.
• W2110366390 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23172703" @default.
• W2110366390 hasPublicationYear "2012" @default.
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