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- W2324777773 endingPage "14737" @default.
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- W2324777773 abstract "The first highly diastereo- and enantioselective additions of a halogen and phosphoramidic acid to unactivated alkenes have been developed, catalyzed by a chiral Brønsted acid. A unique feature of these additions is the opportunity for stereocontrol at two noncontiguous chiral centers, carbon and phosphorus, leading to cyclic P-chiral phosphoramidates. In addition to their inherent value, the phosphoramidates are precursors to enantioenriched epoxy allylamines." @default.
- W2324777773 created "2016-06-24" @default.
- W2324777773 creator A5015166843 @default.
- W2324777773 creator A5041167652 @default.
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- W2324777773 date "2014-10-14" @default.
- W2324777773 modified "2023-10-16" @default.
- W2324777773 title "Brønsted Acid Catalyzed Phosphoramidic Acid Additions to Alkenes: Diastereo- and Enantioselective Halogenative Cyclizations for the Synthesis of <i>C</i>- and <i>P</i>-Chiral Phosphoramidates" @default.
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- W2324777773 doi "https://doi.org/10.1021/ja5088584" @default.
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