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. 2014 Oct 2;6(1):170–173. doi: 10.1039/c4sc02494j

Table 2. Substrate scope a , b , c , d .

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aConditions: nucleophile (1 equiv.), 16 (10 mol%), NaH2PO4 (6 equiv.), ArN2BF4 (1.2 equiv.), cyclohexane (0.025 M).

bConditions: nucleophile (1 equiv.), 17 (10 mol%), NaH2PO4 (6 equiv.), ArN2BF4 (1.2 equiv.), MTBE (0.025 M).

cIsolated yield.

dEnantiomeric excess determined by chiral phase HPLC.