The Staudinger reaction is the initial step in this one-pot sequence. It involves the reduction of an azide compound to an amine using a phosphine reagent. This step is a key feature of the Staudinger reaction, which is a classic organic reaction discovered by Hermann Staudinger.
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N-benzyl-N'-(1-phenylethyl)urea
(3E,5E/Z)-4-Aza-1,1-diphenyl-1,3,5-heptatriene
3-azido-1,2,4,5-tetrafluorobenzene
3,3-dichloro-1-[1-(4-methoxyphenyl)-ethyl]-4-oxo-azetidine-2-carboxylic acid methyl ester
(3R,4S,4'S,5'S) N-(p-anisyl)-3-benzyloxy-4-
endo-7-(methylphenylamino)bicyclo<3.2.0>hept-2-en-6-one
ReC(C6H5)2C(C6H5)2CON(CO)3C10H8N2
(4-nitrobenzylidene)(4-ethoxyphenyl)amine
