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. 2019 Mar 28;15:795–800. doi: 10.3762/bjoc.15.76

Table 1.

Investigation on the effects of substituents on the diastereoselectivity.a

graphic file with name Beilstein_J_Org_Chem-15-795-i001.jpg

Entry Substrate Product, yield,b drc

1 2a (R1 = t-Bu, R2 = t-Bu) (±)-3a, 68%, 14:1 dr
2 2b (R1 = t-Bu, R2 = iPr) (±)-3b, 64%, 3:1 dr
3 2c (R1 = Ph, R2 = t-Bu) (±)-3c, 73%, 2:1 dr
4 2d (R1 = OiPr, R2 = t-Bu) (±)-3d, 78%, 3:1 dr

aReaction conditions: undivided cell, 1 (0.03 mmol), 2 (0.3 mmol), H2O (1 mL), MeCN (9 mL), 3.5 F mol−1. bIsolated yield. cDetermined by 1H NMR analysis of the crude reaction mixture.