Heck reaction alkyne carbopalladation

Tietze and coworkers [60] observed a combination of a Heck reaction and a C-H-activation by treatment of the alkyne 6/1-111 with Pd°. These authors aimed at compound 6/1-112, but 6/1-110 was obtained as a single product in high yield (Scheme 6/1.29). It can again be assumed that after oxidative addition a cis-carbopalladation of the triple bond takes place to give an alkenyl Pd intermediate which undergoes the C-H-insertion into the neighboring naphthalene and not into the aryl ether moiety. 

Currently, there seems to be a widespread tendency to call many reactions proceeding via carbopalladation the Heck reaction. However, this practice is clearly incorrect, since the scope of carbopalladation is significantly wider than that of the Heck reaction. The alkyne carbopalladation reaction shown in Scheme 4, which is not accompanied by /J-dchydropalladation may not be viewed as an example of the Heck reaction. In fact, this chapter focuses its attention on various carbopalladation reactions that may not be considered as examples of the Heck reaction. Although some of such processes are combined with the Heck reaction in many cases. 

A couple of prototypical examples of the cyclic version of the Heck reaction, defined as a process consisting of alkene carbopalladation followed by -elimination, were reported during the 1984-1985 period [9,10]. Almost concurrently, seminal examples of both the non-Heck cyclic carbopallation reactions [10,30] were reported during the 1983-1985 period. Thus, with due respect paid to earlier discoveries of alkyne cyclooligomerization via cascade carbopalladation [7,8] as well as copolymerization [24] and cocyclization [25,... 

A cascade Heck reaction with termination by nucleophiles is considered to start with an oxidative addition of a heteroatom-carbon bond (starter) onto a palladium(O) species (startup reaction), followed by carbopalladation of a nonaromatic carbon-carbon double or triple bond without subsequent dehydropalladation (relay), a second and possibly further carbopalladation of a carbon-carbon double or triple bond (second etc. relay). The terminating step is a displacement of the palladium residue by an appropriate nucleophile. It is crucial for a successful cascade carbopalladation that no premature dehydropalladation takes place, and that can be prevented by using alkynes and 1,1-disubstituted alkenes (or certain cycloalkenes) as relay stations since they give kinetically stable alkenyl- or neopentylpalladium intermediates, respectively. In addition, reaction of haloalkenes with alkenes in certain cases may form rr-allyl complexes, which are then trapped by various nucleophiles. 

Carbopalladation is the reaction of a cr-bonded organopalladium complex I with an unsaturated molecule (such as an alkene 2) to yield the migratory insertion product 3 (Scheme 1). The reaction is tremendously flexible, allowing for a wide variety of structural types for both reactants 1 and 2. The precursors of palladium complexes 1 are commonly alkenyl or aryl halides or triflates (8 and 9, respectively), the reaction of which is more commonly termed the Heck reaction. Allylic systems 10, which react to provide -Tr-allylpalladium complexes, can participate in the reaction as can benzylic precursors 11. Acylpalladium complexes 12 also react and are commonly generated in the same reaction vessel by Pd-catalyzed carbonylation. Their unsaturated reaction partners include alkenes 2, alkynes 4, dienes 6, allenes, and arenes, all of which can be electron rich or poor. Carbopalladation occurs in a syn fashion allowing the installation of stereocenters (2- 3) or control of alkene geometry (4- 5). 

Very recently, the same group [22] performed the synthesis of acenaphthylenes 20 by a combination of a Mizoroki-Heck reaction and an unexpected C—H activation by treatment of a series of alkynes 19 with palladium(O). Acenaphthylenes 20 were obtained as single products in high yields in those cases where R is an aryl moiety. When aliphatic alkynes are used, the yield drops considerably. It can be assumed that, after oxidative addition, a ciT-carbopalladation of the triple bond takes place to give a vinyl-palladium intermediate which undergoes the C—H insertion into the adjacent naphthalene and not into the aryl ether moiety in 19a-e (Scheme 8.4). 

G. S. and Lu, X.Y. (2002) Palladium(II)-catalyzed coupling reactions of alkynes and allylic compounds initiated by intramolecular carbopalladation of alkynes. Tetrahedron Lett., 43, 6791-6794 (d) de Meijere, A. and Meyer, F.E. (1995) Fine feathers make fine birds - the Heck reaction in modem garb. Angew. Chem. Int. Ed., 33, 2379-2411, and references therein. 

Domino or cascade reactions provide valuable approaches, especially to various carbo- and heterocyclic systems with three, four, or even more annelated rings. The Heck reaction has successfully been employed in various inter-inter-, intra-inter-, inter-intra-, as well as all-intramolecular reaction cascades, hi this section, the termination of these processes by alkenes, arenes, and related ir-bond systems such as alkynes and allenes will be described. A cascade Heck reaction is considered to consist of an oxidative addition of a heteroatom-carbon bond to palladium (starter), carbopalladation of a nonaromatic carbon-carbon double or triple bond without immediate dehydropalladation (relay), one, two, or more fimher car-bopalladation(s) of a carbon-carbon double or triple bond, and eventually ensuing dehydropalladation. Crucial for a cascade reaction of this kind to occur is the blockage or retardation of a dehydropalladation at one of the intermediate stages by using 1,1-disubsti-tuted alkenes and appropriately substimted cycloalkenes, bicycloalkenes, or alkynes as relays since they give kinetically stable alkyl- or alkenylpalladium intermediates, respectively. 

Heck Reaction and Related Carbopalladation of Alkenes and Alkynes. 

The successive coordination and iyw-addition of organopalladium(II) intermediates to olefins and alkynes generating a new C—C cr-bond are referred to as migratory insertion or carbopalladation and control the regioselective outcome in the particular reaction. The regiochemistry can be tuned by steric and electronic effects, which will be discussed in more detail for the Heck reaction in Sect. 1.7. 

Recently, Larock and coworkers used a domino Heck/Suzuki process for the synthesis of a multitude of tamoxifen analogues [48] (Scheme 6/1.20). In their approach, these authors used a three-component coupling reaction of readily available aryl iodides, internal alkynes and aryl boronic acids to give the expected tetrasubsti-tuted olefins in good yields. As an example, treatment of a mixture of phenyliodide, the alkyne 6/1-78 and phenylboronic acid with catalytic amounts of PdCl2(PhCN)2 gave 6/1-79 in 90% yield. In this process, substituted aryl iodides and heteroaromatic boronic acids may also be employed. It can be assumed that, after Pd°-cata-lyzed oxidative addition of the aryl iodide, a ds-carbopalladation of the internal alkyne takes place to form a vinylic palladium intermediate. This then reacts with the ate complex of the aryl boronic acid in a transmetalation, followed by a reductive elimination. 

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