Kinetic 1,4-diene formation

The course of intramolecular enone alkene photocycloaddition is dependent on the number of atoms between the two reactive C=C bonds. For example, E- and Z-isomers of 1-acylhepta-1,6-diene (147) form a 1 1 mixture of stereoisomeric cycloadducts 148 and 149 upon irradiation, while no E Z isomerization occurs (Scheme 6.67a).764 The initial bonding takes place between the C2 (Cp) and C6 atoms, in agreement with the empirical rule of five,165 the regioselective, kinetically preferred formation of five-membered ring biradical intermediates over larger rings due to the entropies of cyclization. As a result, the biradical 150 is not observed. For comparison, the acylhexadiene 151 photolysis also proceeds via a 1,4-biradical (152) formed by an initial 1,5-cyclization (Scheme 6.67b).766... 

Diene formation is thought to result from an oxidative-addition mechanism (Scheme 1) rather than edge metalation which leads to snoutanes. Kinetic studies of the Rh -and Pd -catalysed rearrangement of homocubanes to the diene (9) also provide... 

The FMO coefficients also allow cpralitative prediction of the kinetically controlled regioselectivity, which needs to be considered for asymmetric dienes in combination with asymmetric dienophiles (A and B in Scheme 1.1). There is a preference for formation of a o-bond between the termini with the most extreme orbital coefficients ... 

The Diels-Alder reaction of a diene with a substituted olefinic dienophile, e.g. 2, 4, 8, or 12, can go through two geometrically different transition states. With a diene that bears a substituent as a stereochemical marker (any substituent other than hydrogen deuterium will suffice ) at C-1 (e.g. 11a) or substituents at C-1 and C-4 (e.g. 5, 6, 7), the two different transition states lead to diastereomeric products, which differ in the relative configuration at the stereogenic centers connected by the newly formed cr-bonds. The respective transition state as well as the resulting product is termed with the prefix endo or exo. For example, when cyclopentadiene 5 is treated with acrylic acid 15, the cw fo-product 16 and the exo-product 17 can be formed. Formation of the cw fo-product 16 is kinetically favored by secondary orbital interactions (endo rule or Alder rule) Under kinetically controlled conditions it is the major product, and the thermodynamically more stable cxo-product 17 is formed in minor amounts only. 

A special situation is created in a polymerization of isolated dienes or similar compounds like diisocyanates. Addition of such a monomer to a growing polymeric chain leaves its second reactive unit in the vicinity of the active center. Consequently, the addition of this unit is favored to the addition of any other unit, and in fact it is governed by a unimolecular and not bimolecular kinetic law. Its addition leads to the formation of a ring, and if ring closure is... 

Dithiols and dienes may react spontaneously to afford dithiols or dienes depending on the monomer dithiol ratio.221 However, the precise mechanism of radical formation is not known. More commonly, pholoinilialion or conventional radical initiators are employed. The initiation process requires formation of a radical to abstract from thiol or add to the diene then propagation can occur according to the steps shown in Scheme 7.17 until termination occurs by radical-radical reaction. Termination is usually written as involving the monomer-derived radicals. The process is remarkably tolerant of oxygen and impurities. The kinetics of the tbiol-ene photopolymerizalion have been studied by Bowman and... 

Remes et al. (1976) also investigated the kinetics of the N-azo coupling of nine a-amino acids. They are aware of earlier investigations in which the major products were pentaz-1,4-dienes, but they claim that under their reaction conditions (pH 8.00-10.25, thirty-fold excess of amino acid) only the triazenes are formed. The rates were found to be first-order with respect to diazonium ion which is consistent with their conclusion however, in the opinion of the present author the results suggest a significant (say, 10%) contribution of pentazdiene formation to the total rate process. No significant correlation was found between the rate constants and the acidity constants of the nine amino acids. 

We showed (14) that formation of the isomerization products is kinetically controlled and that it depends on the catalyst system employed, the principal conjugated diene isomer being either the trans-2-trans-4-hexadiene, cis-2-trans-4-hexadiene, or 1,3-hexadiene. 

Considering the facility with which dimerization products 81 and 84 are obtained, we reasoned that, in catalytic ring closure of 77, the derived dimer is perhaps initially formed as well. If the metathesis process is reversible [17b], such adducts may subsequently be converted to the desired macrocycle 76. To examine the validity of this paradigm, diene 77 was dimerized (— 85) by treatment with Ru catalyst lb. When 85 was treated with 22 mol% 2 (after pretreatment with ethylene to ensure formation of the active complex), 50-55% conversion to macrolactam 76 was detected within 7 h by 400 MHz H NMR analysis (Eq. 8). When 76 was subjected to the same reaction conditions, <2% of any of the acyclic products was detected. Although we do not as yet have a positive proof that 85 is formed in cyclization of 77, this observation suggests that if dimerization were to occur, the material can be readily converted to the desired macrolactam, which is kinetically immune to cleavage. 

Selectivity in the hydrogenation reaction of dienes to monoenes can be achieved by two types of catalytic system (i) those which are completely inert with respect to the hydrogenation of the resulting monoenes and (ii) those for which the selectivity is due to the discrimination based on thermodynamic and/ or kinetic factors that suppress the rate of formation of the saturated hydrocarbon. The latter approach is the most common way of achieving selectivity for these hydrogenations. 

The above intramolecular diene cyclizations are likely to proceed through a similar set of reactions as shown in Scheme 6.2 for the intermolecular variants. Thus, as depicted in Scheme 6.6, formation of the zirconacyclopropane at the less hindered terminal alkene (—> ii), generation of the tricyclic intermediate iii, Zr—Mg exchange through the intermediacy of zirconate iy and 3-H abstraction and Mg alkoxide elimination in v may lead to the formation of the observed product. Additional kinetic and mechanistic studies are required before a more detailed hypothesis can be put forward. 

The chlorine atom adds in the gas phase to propadiene (la) with a rate constant that is close to the gas-kinetic limit. According to the data from laser flash photolysis experiments, this step furnishes exclusively the 2-chloroallyl radical (2a) [16, 36], A computational analysis of this reaction indicates that the chlorine atom encounters no detectable energy barrier as it adds either to Ca or to Cp in diene la to furnish chlorinated radical 2a or 3a. A comparison between experimental and computed heats of formation points to a significant thermochemical preference for 2-chloroal-lyl radical formation in this reaction (Scheme 11.2). Due to the exothermicity of both addition steps, intermediates 2a and 3a are formed with considerable excess energy, thus allowing isomerizations of the primary adducts to follow. 

In solution, products of central and terminal Br addition to propadiene (la) are formed (Scheme 11.3) [13, 37]. The latter are promoted by high reactant ratios [HBr] [C3H4] and low reaction temperatures. Under conditions of kinetic control, the reaction between diene la and HBr furnishes a 67 33 ratio of allyl bromide 4a versus 2-bromopropene 5a. These investigations also revealed that a-addition of Br is reversible, but the /3-addition is not. The reversible addition to Q has been used to explain the preference for allyl bromide formation from substrate la and H Br at low temperatures, since the Br loss profits from elevated temperatures. 

Thus, fluorination of 1,3-dienes proceeds through an allylic ion, while weakly bridged halonium ions are the intermediates in chlorination and bromination of dienes (vide infra). Furthermore, starting from the experimental evidence that 13 is produced under kinetic conditions and not from subsequent rearrangement of the 1,2- and 1,4-adducts, the authors suggested that 13 arose from rearrangement of the allyl cation intermediate, 17. Consistent with an open ion pair intermediate is also the stereoselective formation of the threo isomer from both 1,3-pentadienes, as well as the preference for the addition to the 1,2-bond observed in the reaction of both isomeric pentadienes. This selectivity may indeed... 

These dications react with alkenes to give 1,2-disulfonium salts, and with conjugated dienes to afford 1,4-adducts. Furthermore, while 1,4-disubstituted linear dienes yield complex mixtures of unidentified substances, 1,3-cyclohexadiene (96) produces a moderately stable salt 102 (equation 106). The formation of the kinetically controlled 1,2-addition product has never been observed. 

For diene ligands which are prochiral, complexation results in the formation of a racemic mixture. Resolution of this racemic mixture has been accomplished via either classical methods102, chromatographic separation on chiral stationary phases103 or kinetic resolution104. For certain acyclic or cyclic dienes possessing a pendent chiral center(s)... 

PbOj anode, 40 155-156 oxygen evolution, 40 109-110 PCE, catalytic synthesis of, l,l,l-trifluoro-2,2-dischloroethane, 39 341-343 7t complex multicenter processes of norboma-diene, 18 373-395 PdfllO), CO oxidation, 37 262-266 CO titration curves, 37 264—266 kinetic model, 37 266 kinetic oscillations, 37 262-263 subsurface oxygen phase, 37 264—265 work function and reaction rate, 37 263-264 Pd (CO) formation, 39 155 PdjCrjCp fCOljPMe, 38 350-351 (J-PdH phase, Pd transformation, 37 79-80 P-dimensional subspace, 32 280-281 Pdf 111) mica film, epitaxially oriented, 37 55-56... 

In the results presented in Table 13.5, the addition of tin affects the kinetic selectivity r differently, depending on the catalyst preparation method. When compared to the monometallic PdO catalyst, r slightly decreases for the coimpregnated PdSn catalyst, but it sharply increases for the PdOSn catalyst prepared via the colloidal oxide synthesis. As the intrinsic kinetic constant rates k do not show significant discrepancies between the different catalysts, the main contribution of the variation of the kinetic selectivity is ascribed to the adsorption constant ratio fBo/ Butenes- In the case of the PdOSn catalyst, formation of but-l-ene is favored compared to its consumption because the X Bo/ Butenes ratio increases, indicating that olefin adsorption is much more destabilized than diene adsorption. Thus, the olefin easily desorbs before being hydrogenated into butane. 

Catalysts lacking phosphorus ligands have also been used as catalysts for allylic substitutions. [lr(COD)Cl]2 itself, which contains a 7i-accepting diolefin ligand, catalyzes the alkylation of allylic acetates, but the formation of branched products was only favored when the substitution reaction was performed with branched allylic esters. Takemoto and coworkers later reported the etherification of branched allylic acetates and carbonates with oximes catalyzed by [lr(COD)Cl]2 without added ligand [47]. Finally, as discussed in Sect. 6, Carreira reported kinetic resolutions of branched allylic carbonates from reactions of phenol catalyzed by the combination of [lr(COE)2Cl]2 and a chiral diene ligand [48]. 

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