1: (Tri-iso-propylsilyl)acetylene With n-butyllithium in tetrahydrofuran; hexane T=-40°C; Metallation; 2: 3-triisopropyl-α,β-acetylenic aldehyde in tetrahydrofuran; hexane T=-40°C; Addition; 0.5 h; Further stages.;
参考文献
Jones, Graham B.; Wright, Justin M.; Plourde, Gary W.; Hynd, George; Huber, Robert S.; Mathews, Jude E.
Journal of the American Chemical Society, 2000 , vol. 122, # 9 p. 1937 - 1944
1.1: n-butyllithium; DMF / tetrahydrofuran / 0.5 h / 20 °C 2.1: n-butyllithium / tetrahydrofuran; hexane / -40 °C 2.2: 97 percent / tetrahydrofuran; hexane / 0.5 h / -40 °C View Scheme
参考文献
Jones, Graham B.; Wright, Justin M.; Plourde, Gary W.; Hynd, George; Huber, Robert S.; Mathews, Jude E.
Journal of the American Chemical Society, 2000 , vol. 122, # 9 p. 1937 - 1944
1: (Tri-iso-propylsilyl)acetylene With potassium dihydrogenphosphate; n-butyllithium Metallation; 2: N,N-dimethyl-formamide Addition; 3: triisopropylsilyl lithium acetylide Alkylation; Further stages.;
参考文献
Jones, Graham B.; Wright, Justin M.; Plourde, Gary W.; Hynd, George; Huber, Robert S.; Mathews, Jude E.
Journal of the American Chemical Society, 2000 , vol. 122, # 9 p. 1937 - 1944