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F-BuOCI

Af-Hydroxypyrazoles 38 and their N -oxides 39 are converted by f-BuOCI to the 4-chloro-47/-pyrazoles 40 and 41, respectively25,26,56 (Scheme 14). Unlike Scheme 6, the reaction proceeds even when R1 and R are alkyl. When... [Pg.62]

If methylcyclopropane is treated with f-BuOCI, various products are obtained but the two major products are C and D. At lower temperatures more of C is formed and at higher temperatures more of D. [Pg.159]


See other pages where F-BuOCI is mentioned: [Pg.128]    [Pg.130]    [Pg.130]    [Pg.131]    [Pg.250]    [Pg.284]    [Pg.81]    [Pg.127]    [Pg.257]    [Pg.257]    [Pg.258]    [Pg.65]    [Pg.546]    [Pg.65]    [Pg.344]    [Pg.639]    [Pg.1202]    [Pg.78]    [Pg.746]    [Pg.363]    [Pg.117]    [Pg.34]    [Pg.279]    [Pg.29]    [Pg.25]    [Pg.1052]    [Pg.329]    [Pg.550]    [Pg.550]    [Pg.551]    [Pg.46]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.125]    [Pg.254]    [Pg.257]    [Pg.303]    [Pg.916]    [Pg.404]    [Pg.405]    [Pg.1631]    [Pg.1958]    [Pg.2517]    [Pg.65]    [Pg.755]    [Pg.414]    [Pg.567]    [Pg.600]   
See also in sourсe #XX -- [ Pg.404 ]




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