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- W2733181877 endingPage "10538" @default.
- W2733181877 startingPage "10535" @default.
- W2733181877 abstract "Abstract BINOL‐based N‐trifluoromethanesulfonyl phosphoramides catalyze the enantioselective (4+3) cycloaddition between furans and oxyallyl cations, the latter being generated in situ by oxidation of allenamides. The chiral organic phosphoramide counteranion is proposed to engage in the activation of the oxyallyl cation intermediate through cooperative hydrogen‐bonding and ion‐pairing interactions, enabling an efficient chirality transfer that provide the final adducts with high diastereo‐ and enantioselectivities. Remarkably, the reaction shows a wide substrate scope that includes a variety of substituted allenamides and furans." @default.
- W2733181877 created "2017-07-14" @default.
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- W2733181877 creator A5088841593 @default.
- W2733181877 creator A5090113111 @default.
- W2733181877 creator A5091142477 @default.
- W2733181877 date "2017-07-26" @default.
- W2733181877 modified "2023-10-17" @default.
- W2733181877 title "Enantioselective Oxidative (4+3) Cycloadditions between Allenamides and Furans through Bifunctional Hydrogen-Bonding/Ion-Pairing Interactions" @default.
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- W2733181877 doi "https://doi.org/10.1002/anie.201704804" @default.
- W2733181877 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28671738" @default.
- W2733181877 hasPublicationYear "2017" @default.