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Iron-mediated allylation reactions

Schobert and co-workers have performed a study on 77 -alkene and 77 -allylcarbene complexes of transition metals. This particularly includes studies on the chemistry of metallacyclic alkenyl complexes of iron, which are reviewed in this chapter. An example of the rf if transformation is shown in Scheme 15. Iron-mediated allylic substitution reactions involve rf rf interconversion and can show chirality transfer.A working hypothesis involves the reaction shown in Scheme 16. [Pg.134]

Fe. Iron metal was found to be able to mediate the allylation reactions of aryl aldehydes with allyl bromide using sodium fluoride as the promoter. The formation of an allyliron species was proposed as the reactive intermediate in the reaction (Scheme 8.20).187 In view of... [Pg.255]

Star polymers and dendrimers have been synthesized by Astruc using cyclopentadienyliron-mediated peralkylation, benzylation, and allylation reactions of cationic tri-, tetra-, and /iexa-methylbenzene cyclopentadienyliron com-plexes. " " These star and dendritic polymers contained cationic cyclopentadienyliron moieties at the core and/or the periphery. The cathodic reduction of nitrates and nitrites to ammonia has been achieved using a water-soluble dendrimer containing six cationic cyclopentadienyliron moieties as a redox catalyst. " The octametallic star (41) was prepared by deprotonation of permethylated iron complexes. ... [Pg.19]

Iron(II) salts, usually in conjunction with catalytic amounts of copper(II) compounds, have also been used to mediate radical additions to dienes91,92. Radicals are initially generated in these cases by reductive cleavage of peroxyesters of hydroperoxides to yield, after rearrangement, alkyl radicals. Addition to dienes is then followed by oxidation of the allyl radical and trapping by solvent. Hydroperoxide 67, for example, is reduced by ferrous sulfate to acyclic radical 68, which adds to butadiene to form adduct radical 69. Oxidation of 69 by copper(H) and reaction of the resulting allyl cation 70 with methanol yield product 71 in 61% yield (equation 29). [Pg.647]

Iron carbonyls also mediate the cycloaddition reaction of allyl equivalents and dienes. In the presence of nonacarbonyldiiron a,a -dihaloketones and 1,3-dienes provide cycloheptenes (Scheme 1.5) [14,15]. Two initial dehalogenation steps afford a reactive oxoallyliron complex which undergoes a thermally allowed concerted [4 + 31-cycloaddition with 1,3-dienes. The 1,3-diene system can be incorporated in cyclic or heterocyclic systems (furans, cyclopentadienes and, less frequently, pyrroles). Noyori and coworkers applied this strategy to natural product synthesis, e.g. a-thujaplicin and P-thujaplicin [14, 16]. [Pg.5]

This reaction has been extended to the reaction between aldehydes and alkenyl complexes of boranes, silanes, and stannes to give allylic alcohols, " where the reaction with alkenyl complexes of silanes is known as the silyl-Prins reaction. In addition, several Lewis acids-mediated or -promoted Prins reactions have recently been developed, including the application of TMSI, hafnium (IV) bis(perfluorooctanesulfonyl)amides (in fluorous biphase system),iron (III) species," and 2,6-di-f rf-butylphenoxy(difluoro)borane. J... [Pg.2276]


See other pages where Iron-mediated allylation reactions is mentioned: [Pg.208]    [Pg.243]    [Pg.360]    [Pg.195]    [Pg.220]    [Pg.151]    [Pg.2087]    [Pg.238]    [Pg.281]    [Pg.185]    [Pg.636]    [Pg.2086]    [Pg.368]    [Pg.184]    [Pg.95]    [Pg.100]    [Pg.522]    [Pg.375]    [Pg.232]    [Pg.256]    [Pg.168]   
See also in sourсe #XX -- [ Pg.236 ]

See also in sourсe #XX -- [ Pg.236 ]




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