853. The cyanoethylation of aryl phosphines
FG Mann, IT Millar
Index: Mann; Millar Journal of the Chemical Society, 1952 , p. 4453,4456
Full Text: HTML
Citation Number: 35
Abstract
4454 Mann and Mallar: the crude product was now apparently purer, since it could be purified by crystallisation without intermediate distillation. Addition of a trace of sodium methoxide to the reaction mixture, however, decreased the yield to 49%. Similarly a mixture
Related Articles:
A practical and expedient synthesis of 2-heterocycle (C–N bond) substituted 4-oxo-4-arylbutanoates
[Khachatryan; Khachikyan; Karamyan; Panosyan; Indzhikyan Chemistry of Heterocyclic Compounds, 2004 , vol. 40, # 4 p. 446 - 451]
A practical and expedient synthesis of 2-heterocycle (C–N bond) substituted 4-oxo-4-arylbutanoates
[Khachatryan; Khachikyan; Karamyan; Panosyan; Indzhikyan Chemistry of Heterocyclic Compounds, 2004 , vol. 40, # 4 p. 446 - 451]
A practical and expedient synthesis of 2-heterocycle (C–N bond) substituted 4-oxo-4-arylbutanoates
[Khachatryan; Khachikyan; Karamyan; Panosyan; Indzhikyan Chemistry of Heterocyclic Compounds, 2004 , vol. 40, # 4 p. 446 - 451]