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Diphenyl phosphoroazidate

Trimethylsilyldiazomethane, 10, 431. An efficient synthesis involves diazo transfer of (CH3)3SiCH2MgCl with diphenyl phosphoroazidate (55-58% yield). ... [Pg.629]

O, N-Dimethylhydroxylamine. Diphenyl phosphoroazidate. lodosylbenzene. Sodium bis(trimethylsilyl)amide. Sodium hydrogen telluride. Triphenylphosphine. [Pg.664]

OH >Nz. Alcohols are converted into azides by treatment with diphenyl phosphoroazidate, triphenylphosphine, and diethyl azodicarboxylate in 60-90% yield. The reaction involves inversion, even in the case of A -stenols. Hindered alcohols are unreactive. ... [Pg.415]

See other pages where Diphenyl phosphoroazidate is mentioned: [Pg.173]    [Pg.217]    [Pg.217]    [Pg.358]    [Pg.193]    [Pg.484]    [Pg.612]    [Pg.415]    [Pg.582]    [Pg.404]    [Pg.173]    [Pg.217]    [Pg.217]    [Pg.358]    [Pg.193]    [Pg.484]    [Pg.612]    [Pg.415]    [Pg.582]    [Pg.404]   
See also in sourсe #XX -- [ Pg.173 ]

See also in sourсe #XX -- [ Pg.217 ]

See also in sourсe #XX -- [ Pg.217 ]

See also in sourсe #XX -- [ Pg.173 ]

See also in sourсe #XX -- [ Pg.193 ]

See also in sourсe #XX -- [ Pg.211 ]



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