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New nickel compounds for alkylation and fluoroalkylation studies
|Burma_Prabhakara Rao_r.pdf||Version for non-UH users. Copying/Printing is not permitted||1.15 MB||Adobe PDF||View/Open|
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|Title:||New nickel compounds for alkylation and fluoroalkylation studies|
|Authors:||Burma, Prabhakara Rao|
|Issue Date:||Dec 2012|
|Publisher:||[Honolulu] : [University of Hawaii at Manoa], [December 2012]|
|Abstract:||Negishi21 introduced zinc reagents as nucleophiles to couple with electrophiles in the formation of C-C bonds. Negishi cross-coupling reactions allowed higher functional group tolerance than other coupling reactions. Negishi used Pd-catalyzed catalysts, homoallylic and homopropargylic alkylzinc reagents and synthesized 1,5-dienes and 1,5-enynes, which constitute the core structure of terpenoids. Negishi found that primary and secondary alkylzinc reagents were more reactive than corresponding alkylmagnesium reagents for the conditions he used. For a very long time coupling reactions were restricted to alkyl-alkyl couplings and sp2 (alkenyl and aryl derivatives) electrophiles. The classical approaches failed in controlling β-hydrogen eliminations when using alkyl halides and pseudohalides. This meant that only methyl, allyl, and benzyl derivatives couple effectively. The problem of β-hydride elimination in palladium-alkyl intermediates could be stopped when used sterically-strong and highly electron donating trialkyl phosphines.22 In this chapter I will go through the development of nickel catalyzed Negishi cross-coupling reactions, because much of my work is focused on understanding these reactions in detail.|
|Description:||M.S. University of Hawaii at Manoa 2012.|
Includes bibliographical references.
|Appears in Collections:||M.S. - Chemistry|
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