Reductive couplings

Reductive polycondensation of 1,1 -diacetyl ferrocene with low-valent titanium, synthesized by a reaction of TiCU with Zn powder [32, 33], yield polymers with ferrocene-vinylene repeating units [34]  

Molar masses up to = 6800 g mol were obtained in the low molar mass area of the GPC, which was calibrated with oligomers given above. 

Ferrocene units have been used as side group, as part of the backbone, as terminating group within various homo and copolymers, crosslinked and swollen polymers, block polymers, and telecheles. For comparison also monomeric compounds and crystallized polymers were studied. Only a few examples may suffice to be mentioned  

The analysis of/below the glass transition Tg reveals very similar behaviour for all the polymers in the temperature range between 50-170 K where nearly harmonic behaviour is found with a temperature 0 2 40-50 K, corresponding to the second moment of the 

Deviations from harmonic behaviour are also found above about 200 K, however, only for the amorphous samples. These high temperature anharmonicities occur often far below Tg, which is typically around 300-350 K. They are supposed to be caused by residual solvents in the polymer matrix. We have also studied / T) for some polymers with a relatively low Tg of 250-300 K. In f T) decreases rapidly following a V c - T dependence as predicted by mode coupling theory (MCT). This is interpreted as the onset of local processes. Tc represents the transition from non-ergodic to ergodic behaviour, which occurs typically 30-150 K above the macroscopic glass transition temperature Tg. In Fig. 15.10 we show f T) for PROPS. The MCT fit is indicated by the broken line yielding Tc = 306 12 K whereas Tg k, 240 K. Simultaneously with the onset of anharmonic behaviour of/the Mofl-bauer resonance lines broaden and quasi-elastic lines appear close to Tc. 

Zinc-mediated reductive dimerization cyclization of 1,1-dicyano-alkenes occurs to give functionaUzed cyclopentenes in good yields under saturated aqueous NH4CI-THF solution at room temperature. The trans isomers are the major products (Eq. 10.38).  

Cyclostannanes (R2Sn) are obtained, primarily as the hexamer (n = 6), by treatment of the diorganotin dichloride R2SnCl2 with sodium naphthalenide [eqn (2.4)].  

When the groups attached to tin are especially bulky, it is possible to isolate the kinetically unstable cyclotristannanes (Ar2Sn)3 (Ar = 2,4,6-R3H2C6, R = Me, 

Aldehydes and ketones can be coupled by employing Woolins reagent (12.366-12.368). 

Numerous isomerisations are promoted by metallophosphine catalysts, but these are often very specific. Reaction (12.369), for example, is effectively promoted by RuCl2(PPh3)3, but the use of Rh(PPh3)3Cl leads to decomposition of the aldehyde product. In reaction (12.370), trans-IrCKCO) (PPh3)2 is very effective but RuCl2(PPh3)3 is quite ineffective. 

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When pyridine is treated with zinc dust and acetic anhydride, a type of reductive coupling occurs and the product is diacetyltetrahydrodipyridyl (I) this undergoes a curious change on heating yielding pyridine and a new diacetyl compound, 1 4 diacetyl 1 4-dihydropyridine (II). The latter is reduced by zinc and acetic acid to 4-ethylpyridine (III). 

Reductive coupling of carbonyl compounds to yield olefins is achieved with titanium (0), which is freshly prepared by reduction of titanium(III) salts with LiAIH4 or with potassium. The removal of two carbonyl oxygen atoms is driven by T1O2 formation- Yields are often excellent even with sensitive or highly hindered olefins. (J.E. McMurry, 1974, 1976A,B). 

The reductive coupling of aldehydes or ketones with 01, -unsaturated carboxylic esters by > 2 mol samarium(II) iodide (J.A. Soderquist, 1991) provides a convenient route to y-lactones (K. Otsubo, 1986). Intramolecular coupling of this type may produce trans-2-hy-droxycycloalkaneacetic esters with high stereoselectivity, if the educt is an ( )-isomer (E.J. Enholm, 1989 A, B). 

Organotelluriumfll and IV) compounds undergo transmetallation with Pd(II)[414], The carbonylation of the alkenylphenyltellurium(II) 459 gives the a,/3-Unsaturated ester 460 and benzoate, 460 being the main product[415], Reductive coupling of diaryl, dialkyl, and aryl alkyltellurides 461 to give 462 proceeds by treatment with Pd(OAc)2[416,417],... 

The reductive coupling of the 7r-allylpalladium enolates 679 gives the allylated ketones. This reaction is also possible thermally, as the Carroll reaction, which... 

Category Ih cyclizations effect closure of the C2 C3 bond. Scheme 3.1 depicts retrosynthetic transformations corresponding to syntheses in category lb. Included are three variations of the intramolecular aldol condensation and reductive coupling of o,/V-diacylanilines,... 

Divalent molybdenum compounds occur in mononuclear, dinuclear, and hexanuclear forms. Selected examples are shown in Figure 6. The mononuclear compounds are mostiy in the realm of organometaUic chemistry (30—32). Seven-coordinate complexes are common and include MoX2(CO)2(PR3)2, where X = Cl, Br, and I, and R = alkyl MoCl2(P(CH3)3)4, heptakis(isonitrile) complexes of the form Mo(CNR) 2 (Fig. 6d), and their chloro-substituted derivatives, eg, Mo(CNR)3CR. The latter undergo reductive coupling to form C—C bonds in the molybdenum coordination sphere (33). 

Compounds with Tin—Tin Bonds. The most important class of catenated tin compounds is the hexaorganoditins. The ditin compounds are usually prepared by reductive coupling of a triorganotin haUde with sodium in Hquid ammonia ... 

Among the appHcations of lower valent titanium, the McMurry reaction, which involves the reductive coupling of carbonyl compounds to produce alkenes, is the most weU known. An excellent review of lower valent titanium reactions is available (195). Titanium(II)-based technology is less well known. A titanium(II)-based complex has been used to mediate a stetio- and regio-specific reduction of isolated conjugated triple bonds to the corresponding polyenes (196). 

Other syntheses of oxiranes which are occasionally useful and involve a species (64) are the dehydration of 1,2-diols (Scheme 69) (78TL5153, 7808(58)12) and the reductive coupling of aldehydes (Scheme 70) (B-73MI50500). 

This procedure is representative of a new general method for the preparation of noncyclic acyloins by thiazol ium-catalyzed dimerization of aldehydes in the presence of weak bases (Table I). The advantages of this method over the classical reductive coupling of esters or the modern variation in which the intermediate enediolate is trapped by silylation, are the simplicity of the procedure, the inexpensive materials used, and the purity of the products obtained. For volatile aldehydes such as acetaldehyde and propionaldehyde the reaction Is conducted without solvent in a small, heated autoclave. With the exception of furoin the preparation of benzoins from aromatic aldehydes is best carried out with a different thiazolium catalyst bearing an N-methyl or N-ethyl substituent, instead of the N-benzyl group. Benzoins have usually been prepared by cyanide-catalyzed condensation of aromatic and heterocyclic aldehydes.Unsymnetrical acyloins may be obtained by thiazol1um-catalyzed cross-condensation of two different aldehydes. -1 The thiazolium ion-catalyzed cyclization of 1,5-dialdehydes to cyclic acyloins has been reported. 

The McMurry reagent reductively couples trifluoroacetophenones to the eorresponding stilbenes [67] (equation 55), and cross-coupling of ketones is also reported [68] (equation 56). 

Reductive Coupling of 4-Methoxy-a,ct,OrTnfIuoroacetophenone cis-and trans-l,1,1,4,4,4-Hexafluoro-2,3-bis(4-methoxyphenyl)-2-butene [67 ... 

Reductive coupling reaction of fluonnated vinyl iodides or bromides has been used as a route to fluorinated dienes [246, 247, 248, 249, 250. Generally, the vinyl iodide is heated with copper metal in DMSO or DMF no 1 ntermediate perfluorovmy I-copper reagent is detected. Typical examples are shown m equations 163-165 [246, 247, 249. The X-ray crystal structure of perfluorotetracyclobutacyclooctatetraene, prepared via coupling of tetrafluoro-l,2-diiodocyclobutene with copper, is planar... 

Reaction with alkali metals in liquid NH3 leads to reductive coupling to give colourless crystals of... 

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