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Lundt and Homeman

An intramolecular radical cyclization on carbohydrate derivatives was the method developed by Lundt and Homeman in a highly stereocontrolled synthesis of functionalized cyclopentanes [9]. Due to the neutral conditions required for the cyclization step, which prevented competing side reactions such as P-elimination and base-promoted epimerization, the potential of the employed radical intramolecular reaction versus the classical carbanionic carbon-carbon bond forming reactions was demonstrated. [Pg.456]


See other pages where Lundt and Homeman is mentioned: [Pg.400]    [Pg.1474]    [Pg.1477]    [Pg.1474]    [Pg.143]   
See also in sourсe #XX -- [ Pg.29 , Pg.456 ]




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Carbafuranose synthesis by Lundt and Homeman

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