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Electrophilic reactions umpolung reduction

Allylstannane 176 is formed by the reaction of allyl acetate with distannanes [97,98], In this reaction, umpolung of the electrophilic 7r-ally] palladium to the nucleophilic allylstannane occurs. Allylation of bromoindole 198 to give allylindole 199 involves the oxidative addition of 198 to Pd, transmetallation with the allylstannane 176, and final reductive elimination [99],... [Pg.130]

Electrophilic reactions on the electron-deficient anthraquinone are normally not possible. However, in 1936 Marschalk described the facile alkylation of the anthraquinone nucleus by aldehydes after reduction of the quinone to the electron-rich hydroquinone using dithionite [34]. This strategy might be called a redox Umpolung , since the chemical reactivity of the anthracene core is reversed by the redox reaction. [Pg.132]

From the retrosynthetic point of view, electrochemical redox reactions are an easy way to accomplish the principle of redox-umpolung (polarity reversal) [2]. As can be seen in Scheme 22.1, oxidation of an electron-rich neutral compound will lead to an electrophilic cation radical, or starting with a nucleophilic anion, anodic oxidation may lead to an electrophilic cation. In the mirror image reductions, an electron-poor neutral compound is transformed to a nucleophilic anion radical, or an electrophilic cation will end up as a nucleophilic anion. [Pg.641]

In the oxidative or reductive versions of the reaction types listed above the [nucleophile, electrophile] combination is not allowed instead we use [nucleophile, nucleophile] combinations oxidatively or [electrophile, electrophile] combinations reductively [R—E, Nu-], [C=C( J-), Nu-], [R—Nu, E+] and [C=C(<5+), E+]. This principle (Umpolung see Section 1) vastly increases the number of choices available for synthetic schemes, and particularly allows for short cuts in conventional ones. Thus, the synthesis of ArOH or ArCN from ArH normally requires four steps (18), whereas the... [Pg.91]

A carbonylation reaction with Ni(CO)4 generating 1,4,7-tricarbonyl compounds has also been published Synthesis of 1,6-dicarbonyl systems via mercury(II) intermediates and radical chain additions to electrophilic olefins has been achieved (equation 70). This sequence constitutes an umpolung if one considers that the carbonyl moiety is masked in siloxycyclopropanes TTireo-juvabione has been synthesized from a methoxycyclo-propane via a mercury(II) salt cleavage/reduction sequence ... [Pg.394]


See other pages where Electrophilic reactions umpolung reduction is mentioned: [Pg.199]    [Pg.446]    [Pg.473]    [Pg.288]    [Pg.547]    [Pg.246]    [Pg.19]   


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