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. 2011 Jun 28;16(7):5460–5495. doi: 10.3390/molecules16075460

Table 2.

ATH of acetophenone catalyzed by 1b in water [a].

Entry Catalyst config. Solution Time; Temp.; Conversion (%) % ee (config) [b] Ref. [c]
1 (R,R) H2O/HCOONa 2 h; 40 °C; >99 94 % (R) [59]
2 (R,R) HCOOH/Et3N 12 h; 40°C; 98 97 % (R) [59]
3 (R,R) H2O/HCOONa/CTAB [d] 4 h; 28 °C; >99 95 % (R) [62]
4 (S,S) H2O/HCOONa/PEG 15 h; 40 °C; >99 96 % (S) [63]

[a] Molar ratio substrate/catalyst (S/C) = 100; The catalyst was formed in situ from the [RuCl26-p-cymene)]2 dimer and TsDPEN; [b] See corresponding references for details on determination of ee and product configuration; [c] Reference containing data for a given entry. [d] CTAB = cetyltrimethyl-ammonium bromide.