Multi-step reaction with 6 steps
1.1: lithium triethylborohydride / tetrahydrofuran / 0.58 h / -78 °C
1.2: H2O2 / tetrahydrofuran; H2O / 0.5 h / 0 °C
2.1: 4900 mg / (p-CH3C6H4)SO3H*H2O / 20 °C
3.1: 76 percent / BF3*Et2O / diethyl ether / 3 h / -78 °C
4.1: O3 / CH2Cl2 / -78 °C
4.2: 63 percent / (CH3)2S / CH2Cl2 / 120 h / 20 °C
5.1: 100 percent / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH2Cl2 / 4 h / 20 °C
6.1: 96 percent / H2; Rh(I)(1,5-COD)(1,2-bis{(R,R)-2,5-di-Et-(c-C4H8P)}C6H4)OTf / methanol / 3878.71 Torr
With
{(1,5-cyclooctadiene)Rh(1,2-bis((2R,5R)-2,5-diethylphospholano)benzene)}triflate; boron trifluoride diethyl etherate; hydrogen; lithium triethylborohydride; toluene-4-sulfonic acid; ozone; 1,8-diazabicyclo[5.4.0]undec-7-ene;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane;
5.1: Horner-Emmons olefination;
DOI:10.1021/jo0203591