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. 2010 Jun 14;107(48):20630–20635. doi: 10.1073/pnas.0914523107

Table 2.

One-pot synthesis of allylic amines using an organocatalytic aziridination-Wharton sequence graphic file with name pnas.0914523107figX20.jpg

Entry
Enone (1)
Product (7)
Yield (%)*
ee (%)
1 1a graphic file with name pnas.0914523107figX21.jpg 7a graphic file with name pnas.0914523107figX22.jpg 56 96
2 1a graphic file with name pnas.0914523107figX23.jpg ent-7a graphic file with name pnas.0914523107figX24.jpg 52 95
3 1b graphic file with name pnas.0914523107figX25.jpg 7b graphic file with name pnas.0914523107figX26.jpg 48 (37)§ 98 (98)§
4 1d graphic file with name pnas.0914523107figX27.jpg 7d graphic file with name pnas.0914523107figX28.jpg 50 (50)§ 97 (97)§
5 1e graphic file with name pnas.0914523107figX29.jpg 7e graphic file with name pnas.0914523107figX30.jpg 57 99
6 1f graphic file with name pnas.0914523107figX31.jpg 7f graphic file with name pnas.0914523107figX32.jpg 61 99
7 1f graphic file with name pnas.0914523107figX33.jpg ent-7f graphic file with name pnas.0914523107figX34.jpg 69 99
8 1g graphic file with name pnas.0914523107figX35.jpg 7g graphic file with name pnas.0914523107figX36.jpg 42 94
9 1h graphic file with name pnas.0914523107figX37.jpg 7h graphic file with name pnas.0914523107figX38.jpg 52 97

*Yields of isolated products.

Determined by chiral stationary phase HPLC.

The quasi-enantiomer of the catalyst was used (2b, see Scheme 5).

§Results for the sequence performed in two separate steps.