反应条件
1: 100 percent / diisobutylaluminium hydride / tetrahydrofuran / 2 h / -78 °C 2: 80 percent / toluene / 6 h / 95 °C 3: 60 percent / pyridinium chlorochromate, toluene-p-sulfonic acid / CH2Cl2 / 12 h / Ambient temperature 4: 87 percent / MeLi, CuCN / tetrahydrofuran / 0.5 h / -78 °C 5: 50 percent / DIBAL-H / diethyl ether / 1 h / -78 °C 6: 87 percent / i-Pr2EtN / CH2Cl2 / 12 h / Ambient temperature 7: 1.) aq. HCl, 2.) LiOH / 1.) THF, room temperature, 14 h, 2.) H2O, MeOH, room temperature, 10 h 8: 1.) Et3N, 2,4,6-trichlorobenzoyl chloride, 2.) N,N-dimethylaminopyridine / 1.) THF, room temperature, 6 h, 2.) toluene, reflux, 14 h 9: 85 percent / TiCl4 / CH2Cl2 / 2 h / 0 °C View Scheme
参考文献
Carnell, Anrdew J.; Casy, Guy; Gorins, Gilles; Kompany-Saeid, Arefeh; McCague, Ray; et al.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1994 , # 23 p. 3431 - 3440