Table 5.
Influence of Trichloroacetamide on Various Donors and Acceptorsa
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Reactions were conducted with donor (0.12 mmol) and acceptor 2 (0.10 mmol) in Et2O (0.2 M), 0 °C, 6 h.
Isolated yields are reported.
The α:β ratios were determined by 1H NMR.
Reactions were conducted with 15 mol % [PhenH]+[BF4]− at 25 °C for 24 h.
Reactions were conducted with 15 mol % of trichloroacetamide as an additive.
The reaction time was 24 h.
Acetonitrile was used as the solvent.
Reactions were conducted with donor (0.10 mmol) and acceptor 4 (0.40 mmol) in THF (0.2 M) 0 °C, 1 h.
Reactions were conducted with donor (0.12 mmol) and acceptor 6 (0.10 mmol) in Et2O (0.2 M), 0 °C, 6 h.