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Hoffmann-Loffler-Freytag

Radical reactions of Hoffmann-Loffler-Freytag type with participation of iodine(III) compounds leading to five-member N-heterocycles 97YGK90. [Pg.246]

Prior to 1958, the only well known examples of functionalization at non activated carbon atoms, in a predictable and specific manner, were those where the Hoffmann-Loffler-Freytag reaction was used. [Pg.264]

En route to the total synthesis of cinchona alkaloid meroquinene, a Hoffmann-La Roehe group took advantage of the Hofmann-Loffler-Freytag reaetion to funetionalize the ethyl side ehain in piperidine 49 to give ehloroethylpiperidine 51 via the intermediaey of protonated aminyl radieal 50. °... [Pg.94]


See other pages where Hoffmann-Loffler-Freytag is mentioned: [Pg.1018]    [Pg.302]    [Pg.25]    [Pg.1018]    [Pg.302]    [Pg.25]   


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Freytag

Hoffmann

Hoffmann-Loffler-Freytag reaction

Loffler

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