Cyclopropenes, reaction with

Reactions with cyclopropene.11 Lithium organocuprates react with the cyclo-propenone ketal 1 (12, 152-154) to form a copper species (a) that behaves as an enolate of a cyclopropanone. Thus it reacts with alkyl halides to form cis-2,3-disubstituted derivatives of 1. 

In some reactions with cyclopropene and 3,3-dimethylcyclopropene, 1 2 adducts were formed which retained the cyclopropane ring, or tautomerized to an azabicyclo[4.1.0]hepta-2,4-diene/ e.g. formation of 2, and 3 and 4. ... 

Reaction with cyclopropenes.8 Reaction of the cyclopropene 1 with Rh2(OAc)4 in C6llft (80°) results in two furans, 2 and 3, in 78% and 3% yield, respectively. Thus the less substituted bond is cleaved selectively. In contrast, treatment of 1 with a Rh(l) catalyst in CH2CI2 at 25° gives only furan 3 in 86% yield. 

The reaction barrier firmly supported our previous finding that 1,3,4-oxadiazole should react with highly reactive dienophiles. In fact, it was predicted that the reaction between 1,3,4-oxadiazole and cyclopropene should be possible under moderate reaction conditions (room temperature). For reactions with dienophiles of low reactivity such as ethylene, forceful reaction conditions or even activation of the diene or dienophile are required. Both 1,3,4-triazole and 1,3,4-thiadiazole were predicted to have activation barriers that were 6 kcal/mol and correspond to comparable reactivities. In all cycloaddition reactions with cyclopropene as a dienophile, an exo cycloadduct is predicted to be a major or exclusive product, which is in agreement with some of our previous studies of cycloaddition reactions with furan as a diene and cyclopropene as a dienophile. 

Tetrakis(triphenylphosphine)palladium(0) Reactions with cyclopropenes ran -a-Trishomobenzenes by trimerization... 

NMR, 3, 542 oxidation, 3, 546 phosphorescence, 3, 543 photoelectron spectra, 3, 542 photolysis, 3, 549 reactions, 3, 543-555 with alkenes, 3, 50 with alkynes, 3, 50 with IH-azepines, 3, 552 with azirines, 3, 554 with cyclobutadiene, 3, 551 with cyclopropenes, 3, 550 with dimethylbicyclopropenyl, 3, 551 with heterocyclic transition metal complexes, 7, 28 29... 

Liquid-phase photolysis of furan atroom temperature occurred in very low yields (1 % conversion), giving a mixture of Diels-Alder adducts deriving from the reaction of cyclopropene-3-carbaldehyde and formylallene with furan (85JOC3034). 

A recent variation of these reactions uses 6/f-l, 3-oxazin-6-ones as the electron-deficient heterodiene in place of the triazine.113114 With cyclopropene at — 35 C oxazinone 45 furnishes the 4//-azepine 46 in excellent yield. Likewise, with 3-methylcyclopropene the 4-methyl derivative 46 (R = Me) is formed. Cycloaddition with 1-methylcyclopropene, however, generates a mixture of 7-tert-butyl, 2-methyl 3-methyl- and 5-methyl-4//-azepine-2,7-dicarboxylate in a 2 1 ratio and a 97 % overall yield. 

The Diels-Alder reaction of cyclopropenes with 1,2,4,5-tetrazines (see Vol.E9c, p 904), a reaction with inverse electron demand, gives isolable 3,4-diazanorcaradienes 1, which are converted into 4H-1,2-diazepines 2 on heating. The transformation involves a symmetry allowed [1,5] sigmatropic shift of one of the bonds of the three-membered ring, a so-called walk rearrangement , followed by valence isomerization.106,107... 

Diphenylcyclopropene thione (156) was prepared11S-12°) from 3,3-dichloro-1,2-diphenyl cyclopropene (154) by reaction with thioacetic acid, since transformation of the carbonyl function of diphenyl cyclopropenone with P4S10121 was complicated by ring expansion to the trithione 155122 In a useful recent thioketone synthesis123) 156 was obtained directly from diphenyl cyclopropenone in a quantitative yield by simultaneous treatment with HC1 and H2S. 

In the category of more elaborate calculations are an SCF—PMO treatment of the reaction of cyclopentadiene with cyclopropene 33>, and calculations including overlap on the photodimerization of linear steroidal dienones. 31> A very fine, detailed theoretical study of thymine photodimerization has been recently presented. 47> Other PMO calculations on photocycloadditions of biochemical interest have also been published. 48>49>... 

The reasons for the ewrfo-selectivity of Diels-Alder reactions are only useful for the reactions of dienophiles bearing substituents with lone pairs without a Lewis basic site no secondary orbital interactions are possible. But even in reactions of pure hydrocarbons the ewrfo-selectivity is observed, requiring alternative explanations. For example, the ewrfo-preference of the reactions of cyclopropene with substituted butadienes have been rationalized on the basis of a special type of secondary orbital interactions70. Apart from secondary orbital interactions which are probably the most important reason for the selec-tivities of Diels-Alder reactions, recent literature also advocates other interpretations. 

The reactions between cyclopropenes and carbon monoxide in the presence of transition metals have been of some use in synthesis,93 and in 1978 Binger initiated a study of the reactions between metal carbonyls and cyclopropenes in order to elucidate the generality of these reactions.75 It was found that dicarbonyl 775-cyclopentadienyl(tetrahydrofuran)manganese(I) reacted with 3,3-dime thy Icy clopropene at 0°C to produce -(vinylketene) complex 81 in fair yield. The only other transition metal in Binger s study that was found to react with 3,3-dimethylcyclopropene in this manner was iron (see Section VI,B). 

In a later paper by Weiss,68 the methodology was extended to a more complex cyclopropene, and an intermediate cobaltacyclobutene (103) was proposed. In an analogous insertion reaction with nonacarbonyldiiron, a vinylcarbene complex was isolated along with the expected vinylketene complex (see Section VI,B). However, no such vinylcarbene cobalt complex was isolated, even when cyclopentadienyl bis(ethene) cobalt was used in place of dicarbonylcyclopentadienyl cobalt, and the only product isolated was the vinylketene complex 104, represented here in the rf -allylacyl structure. 

In the addition of Me2CuLi reagents to electron-deficient acetylenes [85-88], DCD-type complexes have been identified by NMR [84, 89]. As shown below, an ynoate affords a vinylcopper intermediate, while an ynone instead affords an allenolate (Eq. 10.9). The origin of this diversity remains unclear. A related carbocupration mechanism has also been proposed for the reaction with allenylphosphme oxide [53]. Olefin carbocupration of dienes [90] and cyclopropenes [34, 36] is known, but these mechanisms also remain unclear. 

The addition to a carbon-carbon triple bond results in the formation of cyclo-propene products, and with diazoacetates the catalyst of choice for intermolecular addition is the dirhodium(II) carboxamidate 13 (e.g., Eq. 26). The reactions are general, except for phenylacetylene whose cyclopropene product undergoes [2 + 2]-cycloaddition, and selectivities are high. However, high selectivities have not been reported for reactions with allenes. 

Dimerization is an important mode of reaction of strained alkenes, and two different modes of reaction may be found. With cyclopropene, an ene reaction occurs to give a dimer,and this in turn may further react in the same fashion to give a polymer. 

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