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. 2021 Apr 8;86(8):5852–5862. doi: 10.1021/acs.joc.1c00285

Table 2. Conditions and Yields for the One-Pot Synthesis of N-Protected 1-Aminoalkylphosphonium Salts from Amides, Carbamates, Lactams, Imides, or Urea.

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a

Isolated yields.

b

The main reaction product is 2-carbamoylethyltriphenylphosphoniumtetrafluoroborate 14 (78%).

c

The main reaction product is 1,1′-(carbonyldimino)bis(methyltriphenylphosphonium) bis(tetrafluoroborate) 15 (84%; the molar ratio of substrates equals 1(urea): 2:2).