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Asymmetric epoxidation of -undec-2-en-l-ol

The mixture was stirred for 1 hour at — 20 °C and then anhydrous TBHP (7.5 mL, 3.2 M in Ao-octane) also added slowly via a syringe. The mixture was again stirred at —20 °C for 1 hour. (E)-IJndcc-2-cn-1 -oI (1 g, 0.0059 mol) in CH2C12 (5 mL) was added dropwise by syringe such that the temperature was maintained between —15 and — 20 °C. The reaction mixture was stirred at —20 °C for 6 hours and then placed in a freezer overnight. [Pg.83]

Alkene Epoxide Poly(tartrate) % branching Molar ratio alkene Ti tartrate Temperature (°C) Time Isolateda Yield (%) Ee(%) [Pg.85]

Edited by Stan M Roberts and Geraldine Poignant Copyright 2002 John Wiley Sons, Ltd. [Pg.87]

1 Asymmetric epoxidation of disubstituted Z-alkenes using a chiral [Pg.87]

2 Asymmetric epoxidation of disubstituted E-alkanes using a d-fructose [Pg.87]


ASYMMETRIC EPOXIDATION OF ( >UNDEC-2-EN-l-OL USING POLY(OCTAMETHYLENE TARTRATE)... [Pg.81]


See other pages where Asymmetric epoxidation of -undec-2-en-l-ol is mentioned: [Pg.71]    [Pg.82]   


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Asymmetric epoxidation

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Epoxides asymmetric epoxidation

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