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. Author manuscript; available in PMC: 2010 Jul 2.
Published in final edited form as: Org Lett. 2009 Jul 2;11(13):2856–2859. doi: 10.1021/ol901081a

Table 1.

Screen of Michael Acceptors

graphic file with name nihms-123496-f0004.jpg

entry R R' product yield (%)a ee (%)b drc

1 Me Me 8 68 82 6:1
2 Et 9 66 77 14:1
3 Ph Me 10 60 7 14:1
4 Et Me 11 92 89 5:1
5d Me 11 90 92 12:1
a

Reaction conducted with 1 equiv of 7 and 2 equiv of Michael acceptor at 23 °C.

b

Enantiomeric excess determined by HPLC analysis on a chiral stationary phase.

c

Diastereomer ratio determined by 1H NMR.

d

Reaction conducted at 0 °C.