反应条件
1.1: potassium hexacyanoferrate(III); methanesulfonamide; K2OsO4*2H2O; sodium hydrogencarbonate; potassium carbonate; (DHQD)2Pyr / water; tert-butyl alcohol / 72 h / 0 °C
2.1: sulfuric acid / 3 h / 80 °C
3.1: tetrahydrofuran / 1 h / -78 - -70 °C
4.1: hydrogenchloride / methanol / 14 h / 20 °C
5.1: N-bromosuccinmide; 2,2'-azo-bisisobutyronitrile / tetrachloromethane / 0.75 h / |Reflux
6.1: silver perchlorate / tetrahydrofuran / 20 °C / |Inert atmosphere
7.1: toluene-4-sulfonic acid / tetrahydrofuran / 12 h / 0 - 20 °C
8.1: n-butyllithium / tetrahydrofuran / 0.07 h / -78 °C / |Inert atmosphere
8.2: -78 - 20 °C / |Inert atmosphere
9.1: 4-(N,N-dimethlyamino)pyridine; pyridine / 20 °C
10.1: AlCl3, aluminium chloride / nitromethane / 0.5 h / 60 °C / |Acidic conditions; |Microwave irradiation
View Scheme
参考文献
Bachmann, Janina; Mang, Christian; Haustedt, Lars Ole; Harms, Klaus; Koert, Ulrich
European Journal of Organic Chemistry, 2012 , # 33 p. 6562 - 6569