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Cyclic acylpalladations

Cyclic acylpalladation. Another major subtopic of carbopalladation is acylpalladation. In the mid-1960s, two seemingly independent papers were published by J. Tsuji [24] and P.R. Hughes [25,26]. The former reported a perfectly alternating copolymerization of norbornadiene with CO (Scheme 8), while the latter described two related Pd-catalyzed carbonylation cyclizations shown in Scheme 9. [Pg.6]

Development of cyclic acylpalladation of halodienes and haloarylalkenes during the 1983-1985 period [10,30] (Scheme 10) proved to be a breakthrough triggering many subsequent investigations both by the authors group and by others including W. Oppolzer, R. Grigg, and K. Yamamoto. The two discrete cyclic acypalladation reactions shown in Eqs. 1 and 2 of Scheme 10 have been conveniently termed Type I and Type II cyclic acyl-... [Pg.7]

In addition to a couple of reviews focused on results obtained in the authors group [38,39], a comprehensive book on organopalladium chemistry for organic synthesis [40] contains two dozens or so chapters on cyclic car-bopalladation and cyclic acylpalladation. Thus, its Part IV (pi 123-1659) on carbopalladation contains reviews of cyclic carbopalladation on the synthe-... [Pg.10]

Table 1 Effect of ring size ont he competition between cyclic carbopalladation and cyclic acylpalladation in the presence of CO... Table 1 Effect of ring size ont he competition between cyclic carbopalladation and cyclic acylpalladation in the presence of CO...
Ring size Substrate Cyclic carbopalladation Cyclic acylpalladation... [Pg.23]

All of the examples of trapping of acylpalladium species with enolates discussed above as part of the Type III Ac-Pd process involve trapping with O-enolates. As discussed earlier, however, acylpalladium derivatives can also be trapped with C-enolates (Eqs. 4 and 5 in Scheme 11), and this trapping with C-enolates has since been exploited for terminating acyclic carbopalla-dation process [135] (Scheme 48). However, this process does not appear to have been used for terminating cyclic acylpalladation processes. [Pg.38]

Double or Multiple Carbopalladative Cyclization Reactions Involving One or More Cyclic Acylpalladation Processes... [Pg.39]

A systematic investigation of cyclic acylpalladation of haloenes, haloynes, and related electrophiles conducted since 1983 [30] has led to the development of three types of cyclic acylpalladation processes (Types I—III Ac-Pd) and Pd-catalyzed carbonylation-induced ketene [2 + 2] cycloaddition (Sect. 3.1). Collectively, these cyclic acylpalladation and related reactions have provided a number of new and attractive routes to cyclic compounds. Significantly, they nicely complement and supplement the non-carbonylative cyclic carbopalladation reactions. Thus, they have become integral and indispensable parts of the carbopalladation-based cyclization methodology. [Pg.43]


See other pages where Cyclic acylpalladations is mentioned: [Pg.8]    [Pg.8]    [Pg.8]    [Pg.8]    [Pg.8]    [Pg.11]    [Pg.23]    [Pg.32]    [Pg.33]    [Pg.33]    [Pg.34]    [Pg.35]    [Pg.37]    [Pg.38]    [Pg.38]    [Pg.39]    [Pg.39]    [Pg.41]    [Pg.42]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.21]    [Pg.33]    [Pg.42]    [Pg.43]    [Pg.43]    [Pg.44]    [Pg.45]   


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Acylpalladation

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Acylpalladation cyclic

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