Hydroarylation/cyclization

As part of their study on gastric (H+/K+)-ATPase inhibitors, Kang et al. developed a simple and convenient synthetic approach to 1,2,3-trisubstituted pyrrolo[3,2-c]quinolines by means of Pd-catalyzed heteroannulation of 4-amino-3-iodoquinoline derivatives with internal alkynes [76]. The following scheme shows an example of a reaction using 4-arylamino-3-iodoquinoline derivative 180 with alkyne 181 to provide 1-arylpyrrolo [3,2-c]quinoline 182, illustrating the possibility of introducing diverse substituents to 1-arylpyrrolo[3,2-c]quinolines. In addition, a Pd-catalyzed domino hydroarylation/ cyclization process was reported to form substituted quinolines [77]. Thus, 3-arylquino-lines were prepared in 56-74% yield when 3,3-diethyl-l-phenyl-1-propyne and aryl iodide were refluxed in ionic liquid, 1-butyl-3-methylimidazolium tetrafluoroborate [(bmim)BF4 ],in the presence of HCO2H, EtjN, and palladium catalyst. Meanwhile,... 

Cyclization process of arene-yne substrates has been reported with platinum(rv) catalyst (PtCL ), resulting in C-H activation and functionalization.142 This hydroarylation gives 6-< r/o-products in high yields with good tolerance to different functional groups like amine, ester, and ether. This method provides a rapid access to interesting molecules such as coumarins, chromenes, or dihydroquinolines. 

As an extension of the Heck reaction, Pd-catalyzed hydroarylation of alkynes and alkenes continnes to attract high level of research interest in simple couphng processes and in cyclization reactions. The use of this type of transformation as part of a domino reaction will be of increasing interest. The research in the field of domino reactions is attracting considerable attention in synthetic organic chemistry since it enables the rapid assembly of complex molecirles in one-pot processes. Very elegant examples of palladium-catalyzed cascade processes where a single catalytic cycle entails several sequential bond transformations have been recently reported [la, b, 2a, b, c]. 

Scheme 9.23 Metal-dependent cyclization modes in intramolecular alkyne hydroarylation.

Asymmetric cyclization using chiral ligands has been studied. After early attempts[142-144], satisfactory optical yields have been obtained. The hexahy-dropyrrolo[2.3-/)]indole 176 has been constructed by the intramolecular Heck reaction and hydroarylation[145]. The asymmetric cyclization of the enamide 174 using (S)-BINAP affords predominantly (98 2) the ( )-enoxysilane stereoisomer of the oxindole product, hydrolysis of which provides the (5)-oxindole aldehyde 175 in 84% yield and 95% ee. and total synthesis of (—)-physostig-mine (176) has been achieved[146]. 

The palladium-catalyzed hydroboration of allyl phenyl ether 456 is followed by cyclization of the corresponding triflate to afford the chroman core of the tocopheryls 457 (Equation 186) <1998JA9074>. The intramolecular hydroarylation of l-(but-3-enyloxy)-3,5-dimethylbenzene to afford 4,5,7-trimethylchroman can be accomplished using a RuCh/AgOTf catalytic system (Equation 187) <20040L581>. 2,2-Dimethylchromans 458 are formed by a Mo(CO)6 catalyzed intramolecular cyclization of aryl prenyl ethers 459 (Equation 188) <1998S256>. 

Trisubstituted furans were obtained by AuC13- or [(PPh3PAu)2Cl][BF4]-catalyzed hydroarylation reaction of Y-alkynylfurans in good yields, though the product with an exocyclic double bond is not stable <07T5879>. Similar cyclization reaction of furanyl... 

A wide variety of synthetic processes have been rendered asymmetric through the use of a chiral catalyst. In addition to the types of reaction described above, chiral transition metal catalysts have been used to influence the stereochemical course of isomerization, cyclization, and coupling reactions. As an example, an approach towards the natural product (-)-epibatidine (158) was recently reported by Namyslo and Kaufmann (166). Epibatidine is a potent analgesic and a nicotinic receptor agonist. The synthesis involves an asymmetric Heck-type hydroarylation between the bicyclic alkene (155) and pyridyl iodide (156). A number of bidentate chiral li-... 

Palladium(II) catalysts can also be applied to stereo- and regioselective syn hydroarylation and hydrovinylation of symmetrically and unsymmetrically substituted alkynes8 9. Thus, alkyl 4-hydroxy-2-alkynoates in the presence of Pd(OAc)2(PPh3)2, formic acid, and tributylamine in dimethyl formamide or acetonitrile are converted with aryl iodides in a one-pot syn hydroary-lation/cyclization reaction to give functionalized substituted butenolides. The reactions occur with high syn stereoselectivities and with good regioselectivities8. 

The addition of sulfur nucleophiles to alkynes is a less developed transformation. However, Yamamoto described the attack of the sulfur atom of aryl thioethers to afford benzothiophenes (equation 31). More recently, it has been showed that propargylic thioethers or thioacetals undergo migration to give carbenes that cyclize in hydroarylation processes and thiocarbamates that evolve by propargylic rearrangement. Thiosilanes can perform as both sulfur nucleophiles and silicon electrophiles in intramolecular reactions to afford benzothiophenes (equation 32). ... 

The first carbon addition to allenes catalyzed by gold was described by Hashmi and was the addition of furans to allenones, a reaction that is discussed as a conjugate addition to carbonyls. Then the annulation of 2-allenyl indoles was described (equation 111)and an enantioselective version was later developed for terminal allenes. Then Nelson described the cyclization of an N-substituted pyrrol in the synthesis of (—)-Rhazinilam (equation 112). In that case, gold notably improved the yields and selectivities obtained with Pd(II) or Ag(l), and gave complete retention of the chiral information of the allene. The most recent report is on the hydroarylations of allenes with gold-covered substituted benzenes as substrates. ""... 

Phenols have been condensed with alkenoylesters to give chromans by an oxa-Michael addition/electrophilic aromatic addition sequence with magnesium(II)- or copper(II)-bis-oxazoline complexes as chiral Lewis acid catalysts (Scheme 17b) [97]. This reaction may be initiated by an oxa-Michael reaction, followed by a hydroarylation of a carbonyl group. The authors suggest that the initial stereodetermining oxa-Michael addition is followed by a fast diastereoselective aromatic substimtion [97]. A nickel Lewis acid, derived from Ni(hfacac)2 (hfacac = 1,LL5,5,5-hexafluoro-3,5-dioxopentane enolate) and chiral Al-oxide ligands, catalyzes the enantioselective oxa-Michael cyclization of 2-tert-butyloxycarbonyl-2 -hydroxy-chalcones to 3-ferf-butoxycarbonyl flavanones, which can be decarboxylated to flavanons in a separate step (Scheme 17c) [98]. A Lewis acid activation of the unsaturated p-ketoester unit can be assumed. 

Mono-substituted anilines bearing an internal alkyne can be cyclized to quinolines either by metal-mediated hydroarylation of alkynes or through an eleetrophile-mediated Friedel-Craft type reaction. ... 

Hydroarylation of olehns by attack of hydride derived from formic acid is frequently used. Cyclization of 179 generates the neopentylpalladium 180, which is trapped with the hydride to yield the hydroarylation product 181 [88]. 

C.i.a. Sequential Hydroarylation (Hydroalkenylation)/Cyclization. Since the cis stereochemistry of addition pushes the substituents of the acetylenic moiety to the same side of the olefinic double bond, a cyclization reaction can follow the addition step when these substituents bear suitable nucleophilic and electrophilic centers, and the whole process resembles a valuable straightforward methodology for the preparation of cyclic compounds (Scheme 20). Cyclization can occur under hydroarylation(hydroalkenylation) conditions—either before or after the substitution of the carbon-hydrogen bond for the carbon-palladium bond—or by subjecting the isolated hydroarylation(hydroalkenylation) product to suitable reaction conditions. This strategy has been employed successfully to develop new routes to various heterocycles. 

A-vinylindoles took place. Moreover, the gold-catalyzed cyclization of 2-alkynylanilines can be combined with a gold-catalyzed Michael addition to enones, which afforded 3-alkylated indoles with good yield. Gold-catalyzed hydroamination/hydroarylation cascades of polyenyne-substituted anilines leading to condensed aromatics have been described recently. ... 

A reductive Mizoroki-Heck-type cyclization, in which again conformational rigidity thwarts 3-hydride elimination, was reported by Ruchirawat et al. (168 169 Scheme 7.40) [109], who compared the palladium-catalyzed hydroarylation with the alternative radical cyclization, which emerged as less effective. 

In 1993, Murai reported the reactions of aryl ketones witti ethylene and vinylsilanes to form the product from the addition of the C-H bond ortho to the carbonyl group to the olefin (Equation 18.49). This finding led to subsequent work on the addition of the C-H bonds of a variety of aromatic groups to a series of olefins. Catalysts that react under milder conditions than the original ones and extensions of the C-H activation to intramolecular cyclizations to form heterocyclic structures have made this reaction capable of being used in the synthesis of complex molecules. For example, alkylated diterpe-noids and (+)-lithospermic acid (Equations.18.50 and 18.51) have been synthesized using directed hydroarylation. ... 

Youn, S. W., Pastine, S. J. and Sames, D. 2004. Ru(III)-catalyzed cyclization of arene-alkene substrates via intramolecular electrophihc hydroarylation. Org. Lett. 6 581-584. 

In 2000, Hashmi reported the gold(III)-catalyzed cyclization of a-allenyl ketones to form substituted furans [15]. As an example, treatment of allenyl p-methoxybenzyl ketone 70 with a catalytic amount of AuCls formed a 2 1 mixture of the cycloisomerization product 71 and the cycloisomerization/hydroarylation product 72 in 91% combined yield (Eq. (12.40)). Marshall had previously demonstrated the Ag(I)-catalyzed conversion of allenyl ketones to furans [111]. The Ag(I)-catalyzed transformation was four orders of magnitude slower than was the gold(III)-catalyzed transformation, but the silver-catalyzed process forms the 2-substituted furan as the exclusive product without the competing secondary hydroarylation. The selective conversion of a-allenyl ketones to substituted furans is also catalyzed by gold(III)-porphyrin complexes [112]. 

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