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. 2004 Mar 19;101(15):5467–5471. doi: 10.1073/pnas.0307559101

Table 2.

Yield, enantioselectivity, and diastereoselectivity of stilbene oxide from benzaldehyde and benzaldehyde tosylhydrazone salt by using sulfides 1, 5, and 6

graphic file with name zpq011044211t2s1.jpg

Entry Sulfide Yield, %* Trans/cis ee %
1 1 87 >98:2 94 (R, R)
2 6 80 >98:2 86 (R, R)
3 5 83 >98:2 78 (R, R)
*

Yield of isolated product.

Determined by 1H NMR spectroscopy of crude reaction mixture.

Determined by chiral HPLC with a Chiralcel OD column.