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Halovinyl azides

The reaction of iodine azide with haloalkenes 839 followed by elimination of hydrogen halide by potassium fetf-butoxide gives the corresponding halovinyl azides 840, which can be converted into haloazirines 841 by photolysis at —40 C (Scheme 209) <2001T6203>. [Pg.92]

Scheme 5.18 Synthesis of vicinal halovinyl azides (PC = protecting group = acetate or acetal... Scheme 5.18 Synthesis of vicinal halovinyl azides (PC = protecting group = acetate or acetal...
Scheme 5.23 Reactions of vicinal halovinyl azides via 2H-azirines ... Scheme 5.23 Reactions of vicinal halovinyl azides via 2H-azirines ...
See other pages where Halovinyl azides is mentioned: [Pg.129]    [Pg.139]    [Pg.129]    [Pg.139]    [Pg.47]    [Pg.47]   
See also in sourсe #XX -- [ Pg.139 ]



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Vicinal halovinyl azides

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