Diels-Alder , adducts cycloadditions

The simplest of all Diels-Alder reactions cycloaddition of ethylene to 1 3 butadi ene does not proceed readily It has a high activation energy and a low reaction rate Substituents such as C=0 or C=N however when directly attached to the double bond of the dienophile increase its reactivity and compounds of this type give high yields of Diels-Alder adducts at modest temperatures... 

Benzo[Z)]furans and indoles do not take part in Diels-Alder reactions but 2-vinyl-benzo[Z)]furan and 2- and 3-vinylindoles give adducts involving the exocyclic double bond. In contrast, the benzo[c]-fused heterocycles function as highly reactive dienes in [4 + 2] cycloaddition reactions. Thus benzo[c]furan, isoindole (benzo[c]pyrrole) and benzo[c]thiophene all yield Diels-Alder adducts (137) with maleic anhydride. Adducts of this type are used to characterize these unstable molecules and in a similar way benzo[c]selenophene, which polymerizes on attempted isolation, was characterized by formation of an adduct with tetracyanoethylene (76JA867). 

Fluorinated cyclobutanes and cyclobutenes are relatively easy to prepare because of the propensity of many gem-difluoroolefins to thermally cyclodimerize and cycloadd to alkenes and alkynes. Even with dienes, fluoroolefins commonly prefer to form cyclobutane rather than six-membered-ring Diels-Alder adducts. Tetrafluoroethylene, chlorotrifluoroethylene, and l,l-dichloro-2,2-difluoroethyl-ene are especially reactive in this context. Most evidence favors a stepwise diradical or, less often, a dipolar mechanism for [2+2] cycloadditions of fluoroalkenes [S5, (5], although arguments for a symmetry-allowed, concerted [2j-t-2J process persist [87], The scope, characteristic features, and mechanistic studies of fluoroolefin... 

Fluorinaied dienophiles. Although ethylene reacts with butadiene to give a 99 98% yield of a Diels-Alder adduct [63], tetrattuoroethylene and 1,1-dichloro-2,2-difluoroethylene prefer to react with 1,3-butadiene via a [2+2] pathway to form almost exclusively cyclobutane adducts [61, 64] (equation 61). This obvious difference in the behavior of hydrocarbon ethylenes and fluorocarbon ethylenes is believed to result not from a lack of reactivity of the latter species toward [2+4] cycloadditions but rather from the fact that the rate of nonconcerted cyclobutane formation is greatly enhanced [65]... 

In a definitive study of butadiene s reaction with l,l-dichloro-2,2-difluoio-ethylene, Bartlett concluded that [2+4] adducts of acyclic dienes with fluorinated ethylenes are formed through a mixture of concerted and nonconcerted, diradical pathways [67] The degree of observed [2+4] cycloaddition of fluorinated ethylenes IS related to the relative amounts of transoid and cisoid conformers of the diene, with very considerable (i.e., 30%) Diels-Alder adduct being observed in competition with [2+2] reaction, for example, in the reaction of 1,1 -dichloro-2,2-difluoro-ethylene with cyclopentadiene [9, 68]... 

The Diels-Alder adduct isolated from the reaction with 2,3-dimethylbuta-l, 3-diene at elevated temperatures [200] is in fact the product of a two step reaction a 1,3-cycloaddition followed by a 3,2-sigmatropic rearrangement [199] (equaPon 49)... 

A versatile synthetic route to enantiomeric ally pure Diels-Alder adducts was deduced and found dependent on the application of enantiomerically pure 5-methoxy-174a (R=Me) and 5-(l-menthyloxy)-2(5//)-furanones 174b (R = menthyl), which were expected to undergo tt-face-selective cycloaddition with dienes. The reaction was effected by heating no Lewis acid catalysts were required (Scheme 55) (88JOC1127). 

Stable cA-1-phenyl-1-cyclohexene 24 photodimeiizes via Diels Alder cycloaddition to trans adduct 25 (Equation 1.33) [66] and the photoexcitation of dihydrobenzofuran-fused cyclohexenone 26 in net furan gives the trans fused Diels-Alder adduct 27 (Equation 1.34) [67]. 

Diels-Alder reactions of vinylpyrazoles 45 and 46 only occur with highly reactive dienophiles under severe conditions (8-10 atm, 120-140 °C, several days). MW irradiation in solvent-free conditions also has a beneficial effect [40b] on the reaction time (Scheme 4.11). The indazole 48, present in large amounts in the cycloaddition of 45 with dimethylacetylenedicarboxylate, is the result of an ene reaction of primary Diels-Alder adduct with a second molecule of dienophile followed by two [l,3]-sigmatropic hydrogen shifts [42]. The MW-assisted cycloaddition of 46 with the poorly reactive dienophile ethylphenyl-propiolate (Scheme 4.11) is significant under the classical thermal reaction conditions (140 °C, 6d) only polymerization or decomposition products were detected. 

Harano and colleagues [48] found that the reactivity of the Diels-Alder reaction of cyclopentadienones with unactivated olefins is enhanced in phenolic solvents. Scheme 6.28 gives some examples of the cycloadditions of 2,5-bis-(methoxycar-bonyl)-3,4-diphenylcyclopentadienone 45 with styrene and cyclohexene in p-chlorophenol (PCP). Notice the result of the cycloaddition of cyclohexene which is known to be a very unreactive dienophile in PCP at 80 °C the reaction works, while no Diels-Alder adduct was obtained in benzene. PCP also favors the decarbonylation of the adduct, generating a new conjugated dienic system, and therefore a subsequent Diels-Alder reaction is possible. Thus, the thermolysis at 170 °C for 10 h of Diels-Alder adduct 47, which comes from the cycloaddition of 45 with 1,5-octadiene 46 (Scheme 6.29), gives the multiple Diels-Alder adduct 49 via decarbonylated adduct 48. In PCP, the reaction occurs at a temperature about 50 °C lower than when performed without solvent, and product 49 is obtained by a one-pot procedure in good yield. 

An interesting parallel was found while the microwave-enhanced Heck reaction was explored on the C-3 position of the pyrazinone system [29]. The additional problem here was caused by the capability of the alkene to undergo Diels-Alder reaction with the 2-azadiene system of the pyrazinone. An interesting competition between the Heck reaction and the Diels-Alder reaction has been noticed, while the outcome solely depended on the substrates and the catalyst system. Microwave irradiation of a mixture of pyrazinone (Re = H), ethyl acrylate (Y = COOEt) and Pd(dppf)Cl2 resulted in the formation of a mixture of the starting material together with the cycloaddition product in a 3 1 ratio (Scheme 15). On the contrary, when Pd(OAc)2 was used in combination with the bulky phosphine ligand 2-(di-t-butylphosphino)biphenyl [41-44], the Heck reaction product was obtained as the sole product. When a mixture of the pyrazinone (Re = Ar) with ethyl acrylate or styrene and Pd(dppf)Cl2 was irradiated at 150 °C for 15 min, both catalytic systems favored the Heck reaction product with no trace of Diels-Alder adduct. 

Grieco utilized an aqueous intermolecular Diels-Alder reaction as the key step in forming the AB ring system of the potent cytotoxic sesquiterpene vernolepin. 87 Cycloaddition of sodium ( >3,5-hexa-dienoate with an a-substituted acrolein in water followed by direct reduction of the intermediate Diels-Alder adduct gave the desired product in 91% overall yield (Eq. 12.28). 

Reactions favoring [2 + 2] cycloaddition tended to be those that had strongly electronegative groups on the sp2-hybridized silicon but only H and the neopentyl group on the sp2-hybridized carbon atom. Butadiene and cyclohexadiene generally favored [2 + 2] cycloaddition with these silenes. The [2 + 2] adducts with cyclohexadiene appear to be kinetic products, since they cleanly isomerized to the Diels-Alder adducts over time.182... 

The reaction of nitrostyrene with cyclopentadiene gives the normal Diels-Alder adduct. However, the Lewis acid-catalyzed cycloaddition affords two isomeric nitronates, syn and anti in an 80-to-20 ratio. The major isomer is derived from an endo transition state. The preference of yy/i-fused cycloadducts can be understood by considering secondary orbital interactions (Eq. 8.95).152... 

Whereas the parent MCP (1) is not reported to give [4 + 2] cycloadditions, bicyclopropylidene (3) has been shown to give Diels-Alder adducts. Bicyclo-propylidene (3) is a unique olefin, combining the structural features of a tetra-substituted ethylene and two methylenecyclopropane units. The central... 

The same authors showed that microwave irradiation can alter the reaction pathway. Occasionally with conventional heating the Diels-Alder adducts are favored whereas the tandem [6+4]—[4+2] cycloaddition products were obtained exclusively under the action of microwaves [86 b]. 

The critical role of the ion-radical pair in the cycloaddition reactions in equation (75) is demonstrated by a careful measurement of the quantum yields as a function of the dienophile concentration and by a study of the effect of solvent and salt on the dynamics of the ion pair ANT+ , MA-. 212 However, in the reported cases, back electron transfer effectively competes with the coupling within the ion-radical pair and thus limits the quantum yields for the formation of the Diels-Alder adduct.212... 

The partially hydrogenated phenanthrene derivative 18 (entry 4) is a very moderate diene due to the steric crowding caused by the substituents and the anulated rings, and it reacts even with highly reactive dienophiles such as maleic anhydride (MA) or N-phenylmaleic imide only at high pressure. The minor product 20 in the reaction with MA obviously stems from diene 21. This can be explained by a double-bond isomerization 18 - 21 prior to the cycloaddition, certainly catalyzed by traces of acid present in the MA. In the absence of acid only the Diels-Alder adduct 22 derived from diene 18 was observed. In the reaction of diene 23 with MA (entry 5) a similar sequence of steps was observed. A [1,5] shift of the C—O bond in 23, again certainly acid-catalyzed, produces the diene 26 followed by the Diels-Alder reaction with MA to give 24 and 25. 

In the presence of a catalytic amount of chiral lanthanide triflate 63, the reaction of 3-acyl-l,3-oxazolidin-2-ones with cyclopentadiene produces Diels-Alder adducts in high yields and high ee. The chiral lanthanide triflate 63 can be prepared from ytterbium triflate, (R)-( I )-binaphthol, and a tertiary amine. Both enantiomers of the cycloaddition product can be prepared via this chiral lanthanide (III) complex-catalyzed reaction using the same chiral source [(R)-(+)-binaphthol] and an appropriately selected achiral ligand. This achiral ligand serves as an additive to stabilize the catalyst in the sense of preventing the catalyst from aging. Asymmetric catalytic aza Diels-Alder reactions can also be carried out successfully under these conditions (Scheme 5-21).19... 

When irradiated with light, azidodicarboxylates react with glycals as dienophiles to give Diels-Alder adducts via formal [4 + 2] cycloadditions [334], Upon treatment of... 

Evans et al. (219, 220) examined the use of electron-poor heterodienes as partners in cycloadditions with electron-rich alkenes under copper catalysis. In particular, a,p-unsaturated acylphosphonates and keto-esters afford hetero-Diels-Alder adducts in high selectivities when treated with enol ethers in the presence of catalysts 269c and 269d. 

Various substituted unsaturated acylphosphonates participate in highly dias-tereoselective and enantioselective cycloadditions with vinyl ethers, Eqs. 177 and 178. It is intriguing to note that catalysts [(.V,.Y)-f-Bu-box]Cu (OTf)2 (269c) and [(.V,.S )-Ph-box]Cu (OTf>2 (269d) possessing the same sense of chirality afford opposite antipodes of the cycloadduct in comparable selectivities. Cyclopentadiene was found to react with acylphosphonates to give a mixture of the normal Diels-Alder adduct and the inverse electron demand hetero-Diels-Alder adduct (35 65), Eq. 179. This result may be contrasted with crotonylimide, which furnishes the normal demand Diels-Alder adduct exclusively. 

Cycloaddition between the vinyl sulfoxide 276 and 1,3-cyclopentadiene (277) takes place readily to yield the Diels-Alder adduct 278, which, when heated in pyridine, undergoes a /3-elimination to provide 279, the formal adduct of allene (1) to 277 (Scheme 5.42) [115]. 

Reacting 126 with dienophiles 283 produces Diels-Alder adducts 284, which, as cydobutenes, can thermally be ring opened to the conjugated dienes 285, ready for a repetition of the cycloaddition step to provide the 2 1 adducts 286. Hence the whole sequence represents a diene-transmissive Diels-Alder protocol [118]. 

Seitz and colleagues108 made 10-ethylcolchicide (138), a colchicine derivative, react with several dienophiles. The reaction of 138 with dimethyl acetylenedicarboxylate (57) afforded a single Diels-Alder adduct (139) which underwent a consecutive [3 + 2] cycloaddition with another equivalent of dimethyl acetylenedicarboxylate to give 140. The formal elimination of C2H6 afforded 141, whereas fragmentation led to 142 (equation 41). 

---