(4S,7aR)-7a-甲基-1-[(2S)-1-氧代-2-丙基]八氢-1H-茚-4-基苯甲酸酯合成路线 (共 1 条)
反应条件
1: 1) 2,6-di-tert-butylpyridine, 2a) TMSTf, 2b) Et3N, MeOH / 1) CH2Cl2, -78 deg C, 5 min, 2a) -78 deg C, 2 h, 2b) -78 deg C, 5 min then to RT 2: TiCl4 / CH2Cl2 / 12 h / -78 °C 3: 92 percent / DMAP, i-Pr2NEt / CH2Cl2 / 18 h / 0 °C 4: 91 percent / LDA / tetrahydrofuran / 0.5 h / -78 °C 6: 1) LDA / 1) -78 deg C 7: 94 percent / Et3N / (Ph3P)2PdCl2 / 75 °C 8: H2, Lindlar catalyst, quinoline / hexane 9: 2,2,4-trimethyl-pentane / Heating 10: 82 percent / ion-exchange resin AG 50W-X4 / methanol / 48 h / Ambient temperature; in the dark View Scheme
参考文献
Granja; Castedo; Mourino
Journal of Organic Chemistry, 1993 , vol. 58, # 1 p. 124 - 131