## Abstract Reactions of organolithium compounds with alkyl halides and with epoxides are considerably accelerated by addition of equivalent amounts of potassium __tert__βbutoxide.
Alkylation of carbonyl compounds with dialkylzirconocene complexes promoted by potassium t-butoxide
β Scribed by Ann L. Larson; Diana L. Baker; Robert W. Towne; Daniel A. Straus
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 172 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Potassrum r-butoxlde promotes alkylation of non-enohzable ketones and aldehydes by zlrconocene dmlkyls The reaction proceeds wdh loss of cyclopentachemde Ion from the metal center Organozlrcomum complexes are finding Increasing use In orgamc synthesis 1 The maJorlty of developments m this area mvolve bls($-cyclopentadlenyl)wrcomum ("zlrconocene") denvatlves Whereas complexes of the type RZr(OR')j have long been known to react as nucleophlles toward carbonyl substrates,* zlrconocene alkyls do not, transmetalafion has ken used previously to overcome this hnutatlon 3 We report here that addmon of 4-5 eq of KOt-Bu to a THF solution of Cp2ZrR2
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