反应条件
1.1: various solvent(s) / 1 h / 240 °C 2.1: TsOH; MeOH / CH2Cl2 3.1: Et3N; DMAP / CH2Cl2 4.1: Pd(OAc)2; DPPP; Bu4NOAc / 1 h / 20 °C 4.2: NaBH4 4.3: NaOMe; MeOH 5.1: (COCl)2; DMSO; Et3N 6.1: tetrahydrofuran / -78 - 20 °C 7.1: (COCl)2; DMSO; Et3N / CH2Cl2 8.1: tBuOK / tetrahydrofuran 8.2: 75 percent / tetrahydrofuran / 4 h / -30 - 20 °C 9.1: AcOH; H2O / tetrahydrofuran / 24 h / 20 °C 10.1: NaBH4 / methanol 11.1: CBr4; PPh3 / acetonitrile / 0 °C 11.2: 91 percent / 2,6-di-tert-butyl-4-methylpyridine / acetonitrile / -40 °C 12.1: tetrahydrofuran / -78 °C 13.1: LiHMDS / tetrahydrofuran / -78 °C 13.2: 80 percent / tetrahydrofuran 14.1: TMSOTf; collidine / CH2Cl2 / 1 h / 0 °C 14.2: 85 percent / nBu4NF / tetrahydrofuran 15.1: 2,4,6-trichlorobenzoyl chloride; Et3N / tetrahydrofuran / 1 h / 20 °C 15.2: 60 percent / DMAP / toluene / 80 °C 16.1: 86 percent / TFA / CH2Cl2 / 0 °C 17.1: 71 percent / 2,4,6-triisopropylbenzenesulfonyl hydrazide; Et3N / diethyl ether / 39 °C 18.1: dimethyldioxirane / CH2Cl2 / -50 °C View Scheme
参考文献
Ermolenko, Mikhail S; Potier, Pierre
Tetrahedron Letters, 2002 , vol. 43, # 16 p. 2895 - 2898