反应条件
1.1: lithium diisopropylamide / tetrahydrofuran / 0.08 h / -78 °C
1.2: trimethylchlorosilane / tetrahydrofuran / 3 h / Heating
1.3: methanol / 0.17 h / 20 °C
2.1: 97 percent / diethyl ether
3.1: 91 percent / DIBAL-H / toluene / 1 h / 20 °C
4.1: 90 percent / pyridine
5.1: 84 percent / dimethylsulfoxide / 2 h / 80 °C
6.1: 79 percent / 20percent KOH / bis-(2-hydroxy-ethyl) ether / 1 h / Heating
7.1: 97 percent / diethyl ether
8.1: 80 percent / DIBAL-H / toluene / 1 h / 20 °C
9.1: 98 percent / pyridine
10.1: 69 percent / ozone; triphenylphosphane / CH2Cl2; methanol
11.1: hydroxylamine hydrochloride; sodium acetate / ethanol
12.1: 1.19 g / sodium acetate / acetic anhydride / Heating
13.1: potassium hydroxide / methanol / 2 h / Heating
14.1: 95 percent / triphenylphosphane / CCl4 / 2 h / Heating
15.1: 91 percent / 1 h / 130 °C
View Scheme
参考文献
Brenna, Elisabetta; Fuganti, Claudio; Grasselli, Piero; Serra, Stefano
European Journal of Organic Chemistry, 2001 , # 7 p. 1349 - 1357