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. Author manuscript; available in PMC: 2010 Jun 21.
Published in final edited form as: Synlett. 2009 May;8(2009):1189–1207. doi: 10.1055/s-0029-1216654

Table 8.

Formation of quaternary stereocenters from aromatic aldehydes via the asymmetric Stetter reaction. graphic file with name nihms-199310-t0117.jpg

Entry Substrate Product Yield % ee%
1 graphic file with name nihms-199310-t0118.jpg graphic file with name nihms-199310-t0119.jpg 96 97
2 graphic file with name nihms-199310-t0120.jpg graphic file with name nihms-199310-t0121.jpg 92 89
3 graphic file with name nihms-199310-t0122.jpg graphic file with name nihms-199310-t0123.jpg 95 99
4 graphic file with name nihms-199310-t0124.jpg graphic file with name nihms-199310-t0125.jpg 95 92
95a 92a
5 graphic file with name nihms-199310-t0126.jpg graphic file with name nihms-199310-t0127.jpg 54 87
83a 98a
6 graphic file with name nihms-199310-t0128.jpg graphic file with name nihms-199310-t0129.jpg 33 88
91a 99a
7 graphic file with name nihms-199310-t0130.jpg graphic file with name nihms-199310-t0131.jpg 11 82
15a 82a
8b graphic file with name nihms-199310-t0132.jpg graphic file with name nihms-199310-t0133.jpg 55 99
9 graphic file with name nihms-199310-t0134.jpg graphic file with name nihms-199310-t0135.jpg 0 ---
11c >99c
a

KOt-Bu was used as the base.

b

Catalyst added in two portions.

c

Catalyst 40 was used.