反应条件
1.1: TEA / CH2Cl2 / 3 h / 0 °C
2.1: 92 percent / K2CO3; MeSO4NH2; K2OsO2(OH)4 / (DHQD)2PHAL / 2-methyl-propan-2-ol / 2 h / 0 °C
3.1: p-TsOH / 1 h / 20 °C
4.1: Zn(NO3)2*6H2O / acetonitrile / 3 h / 50 °C
5.1: Bu2SnO / toluene / 12 h / Heating
5.2: 84 percent / Bu4NI / 1.5 h / Heating
6.1: 100 percent / 2,6-lutidine / CH2Cl2 / 0.5 h / 0 °C
7.1: 87 percent / KOH / methanol; tetrahydrofuran / 1 h / 20 °C
8.1: TPAP; NMO; 4 Angstroem molecular sieves / CH2Cl2 / 1 h / 20 °C
9.1: DBU; LiCl / acetonitrile / 2.5 h / 20 °C
10.1: 85 percent / (R)-BINAl-H / tetrahydrofuran / 6 h / -100 °C
11.1: 92 percent / p-TsOH / benzene / 0.5 h / Heating
12.1: 94 percent / NaHMDS; TMSCl / tetrahydrofuran / 4 h / -78 °C
13.1: 94 percent / H2O2; NaHCO3 / ethyl acetate; tetrahydrofuran / 0.5 h / 20 °C
14.1: 96 percent / DDQ; water / CH2Cl2 / 0.5 h / 20 °C
15.1: Dess-Martin periodinane; NaHCO3 / CH2Cl2 / 1 h / 20 °C
16.1: NaHMDS / hexamethylphosphoric acid triamide; tetrahydrofuran / -100 - 0 °C
17.1: 89 percent / HCl / methanol / 10 h / 20 °C
18.1: 2,6-lutidine / 0.17 h / -78 °C
19.1: -78 - 20 °C
20.1: 70 percent / HCl / tetrahydrofuran; acetonitrile / 2 h / -10 °C
21.1: 80 percent / PdCl2(MeCN)2 / dimethylformamide / 25 h / 20 °C
22.1: PCl3; pyridine
22.2: 56 percent / TBHP / CH2Cl2
23.1: HF / acetonitrile
23.2: 38 percent / pyridine / 20 h / 20 °C
View Scheme
参考文献
Miyashita, Kazuyuki; Ikejiri, Masahiro; Kawasaki, Hitomi; Maemura, Satoko; Imanishi, Takeshi
Chemical Communications, 2002 , # 7 p. 742 - 743