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- W2950441445 endingPage "3326" @default.
- W2950441445 startingPage "3319" @default.
- W2950441445 abstract "Abstract We describe herein an approach to the total synthesis of functionalized pyrrolizidinones and pyrrolizidines. The synthetic sequence is based on a highly stereoselective substrate-controlled Morita–Baylis–Hillman (MBH) reaction between a chiral amino-aldehyde and methyl acrylate. The selectivity attained in this reaction was controlled by the presence of a hydroxyl group adequately placed in the structure of the amino-aldehyde used as the nucleophilic component of the MBH reaction. The MBH adducts were used as substrate for an efficient total synthesis of pyrrolizidinones and pyrrolizidines in good overall yield." @default.
- W2950441445 created "2019-06-27" @default.
- W2950441445 creator A5003233715 @default.
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- W2950441445 creator A5048709574 @default.
- W2950441445 creator A5064926059 @default.
- W2950441445 creator A5076119963 @default.
- W2950441445 creator A5079847870 @default.
- W2950441445 date "2014-05-01" @default.
- W2950441445 modified "2023-10-10" @default.
- W2950441445 title "An asymmetric substrate-controlled Morita–Baylis–Hillman reaction as approach for the synthesis of pyrrolizidinones and pyrrolizidines" @default.
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