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- W47356903 endingPage "876" @default.
- W47356903 startingPage "838" @default.
- W47356903 abstract "Hydrozirconation of alkenes and alkynes gave functionalized alkanes and stereodefined functionalized alkenes under mild conditions in high yields. For this purpose, commercially provided or in situ generated Cp 2 ZrHCl (Schwartz reagent) is frequently used. The bulky zirconocene moiety is the critical factor for this big success. It leads to the high regioselectivity during hydrozirconation, and it also contributes to good functional group tolerance by sheltering the reactive point. The alkyl and alkenylzirconium complexes subsequently react with electrophiles to form various C C(X) or C C(X) bonds. To obtain higher or diverse reactivity, transmetalation can be employed to produce widespread synthetic applications." @default.
- W47356903 created "2016-06-24" @default.
- W47356903 creator A5042033606 @default.
- W47356903 creator A5059101214 @default.
- W47356903 date "2014-01-01" @default.
- W47356903 modified "2023-09-26" @default.
- W47356903 title "8.23 Hydrozirconation of Alkenes and Alkynes" @default.
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