diphosphorous tetraiodide in dichloromethane 0 degC, 25 min and room temp., 5 min;

Multi-step reaction with 3 steps 1: 92 percent / trioctylphosphine, carbon tetrabromide / diethyl ether / 0.22 h / 0 °C2: 1.) butyllithium, 2.) 3-methoxy-3-methylbut-1-ynylcopper3: 1.) LiAlH4, 2.) PCC, AcONa / 1.) Et2O, 10 min, 2.) dichloromethane, RT, 1 h  

Multi-step reaction with 4 steps 1: 92 percent / pyridinium p-toluenesulfonate / ethanol / 4 h / 50 °C2: 92 percent / trioctylphosphine, carbon tetrabromide / diethyl ether / 0.22 h / 0 °C3: 1.) butyllithium, 2.) 3-methoxy-3-methylbut-1-ynylcopper4: 1.) LiAlH4, 2.) PCC, AcONa / 1.) Et2O, 10 min, 2.) dichloromethane, RT, 1 h  

Multi-step reaction with 5 steps 1: 65 percent / AgBF4 / benzene / 2.5 h / 80 °C2: 92 percent / pyridinium p-toluenesulfonate / ethanol / 4 h / 50 °C3: 92 percent / trioctylphosphine, carbon tetrabromide / diethyl ether / 0.22 h / 0 °C4: 1.) butyllithium, 2.) 3-methoxy-3-methylbut-1-ynylcopper5: 1.) LiAlH4, 2.) PCC, AcONa / 1.) Et2O, 10 min, 2.) dichloromethane, RT, 1 h  

With  lithium aluminium tetrahydride; Pyr*CrO3*HCl  1.) Et2O;  Yield given. Multistep reaction;   

Multi-step reaction with 2 steps 1: 1.) butyllithium, 2.) 3-methoxy-3-methylbut-1-ynylcopper2: 1.) LiAlH4, 2.) PCC, AcONa / 1.) Et2O, 10 min, 2.) dichloromethane, RT, 1 h