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- W2950867085 abstract "A procedure for one-pot intermolecular radical addition of 2-iodoesters to terminal alkenes followed by azidation of the radical adduct has been developed. This sequential reaction represents an alkene carboazidation process. Its efficacy is demonstrated by the two-step preparation of various lactams such as pyrrolidinones, pyrrolizidinones, and indolizidinones. An easy access to spirolactams bearing an amino-substituted quaternary carbon center is also described. These compounds are important building blocks for the synthesis of numerous alkaloids such as, for instance, FR901483." @default.
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- W2950867085 date "2004-08-17" @default.
- W2950867085 modified "2023-09-23" @default.
- W2950867085 title "Radical Carboazidation: Expedient Assembly of the Core Structure of Various Alkaloid Families." @default.
- W2950867085 cites W2147183053 @default.
- W2950867085 doi "https://doi.org/10.1002/chin.200433215" @default.
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