Multi-step reaction with 8 steps
1: 93 percent / diisobutylaluminum hydride / diethyl ether / 1 h / -78 °C
2: 80 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone; molecular sieves 4 Angstroem / CH2Cl2 / 5 h / 0 °C
3: 100 percent / 2,4,6-trichlorobenzoyl chloride; 4-(dimethylamino)pyridine; Et3N / toluene / 1.5 h / -78 - 20 °C
4: 20 percent / lithium borohydride; EtOH / diethyl ether / 3.5 h / -10 °C
5: 83 percent / NaH / tetrahydrofuran / 3 h / 20 °C
6: 90 percent / 2,4,6-trichlorobenzoyl chloride; 4-(dimethylamino)pyridine; Et3N / toluene / 1.5 h / -78 - 20 °C
7: 80 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / CH2Cl2; aq. phosphate buffer / 3 h / 0 °C
8: 94 percent / Dess-Martin periodinane / CH2Cl2 / 1 h / 20 °C
With
dmap; lithium borohydride; ethanol; 4 A molecular sieve; 2,4,6-trichlorobenzoyl chloride; sodium hydride; diisobutylaluminium hydride; Dess-Martin periodane; triethylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone;
In
tetrahydrofuran; phosphate buffer; diethyl ether; dichloromethane; toluene;
3: Yamaguchi esterification / 6: Yamaguchi esterification;
DOI:10.1002/anie.200504573