Stereochemistry free-radical, with

The side chain can also affect electronic events of the tricyclic ring system. Electron spin resonance experiments allowed Fenner S to suggest that the influence of the side chain of phenothiazine on the formation of free radicals showed a correlation between the redox activity of the phenothiazine nucleus and dynamic aspects of stereochemistry. For example, there was a difference in the formation of cationic free radicals between promazine and alimemazine. The latter has a branched side chain, and forms cationic free radicals only under irradiation. It differs from promazine in pharmacodynamic properties, reported s to result in considerably shifted ion exchange equilibria. A kinetic study of the oxidation of dopamine by dialkylaminoalkyl phenothiazine cationic free radicals showed that a strong correlation existed between side-chain structures and oxidation rates phenothiazine free radicals with two carbon side chains had faster rates than those with three carbon side diains, albeit both were very rapid at physiological pH. 

Decomposition of the /rtin -decalyl perester A gives a 9 1 ratio of trans cis hydroperoxide product at all oxygen pressures studied. The product ratio from the cis isomer is dependent on the oxygen pressure. At 1 atm O2, it is 9 1 trans cis, as with the trans substrate, but this ratio decreases and eventually inverts with increasing O2 pressure. It is 7 3 cis trans at 545 atm oxygen pressure. What deduction about the stereochemistry of the decalyl free radical can be made from these data ... 

Some instances of incomplete debromination of 5,6-dibromo compounds may be due to the presence of 5j5,6a-isomer of wrong stereochemistry for anti-coplanar elimination. The higher temperature afforded by replacing acetone with refluxing cyclohexanone has proved advantageous in some cases. There is evidence that both the zinc and lithium aluminum hydride reductions of vicinal dihalides also proceed faster with diaxial isomers (ref. 266, cf. ref. 215, p. 136, ref. 265). The chromous reduction of vicinal dihalides appears to involve free radical intermediates produced by one electron transfer, and is not stereospecific but favors tra 5-elimination in the case of vic-di-bromides. Chromous ion complexed with ethylene diamine is more reactive than the uncomplexed ion in reduction of -substituted halides and epoxides to olefins. ... 

From the point of view of both synthetic and mechanistic interest, much attention has been focused on the addition reaction between carbenes and alkenes to give cyclopropanes. Characterization of the reactivity of substituted carbenes in addition reactions has emphasized stereochemistry and selectivity. The reactivities of singlet and triplet states are expected to be different. The triplet state is a diradical, and would be expected to exhibit a selectivity similar to free radicals and other species with unpaired electrons. The singlet state, with its unfilled p orbital, should be electrophilic and exhibit reactivity patterns similar to other electrophiles. Moreover, a triplet addition... 

Most of the results recently reported in this field relate to free-radical cyclisa-tions (Eq. 9) which are useful processes to make mainly five-membered rings via the 5-exo-trig mode, with eventually a given stereochemistry [65] ... 

Conjugated dienes such as 1,3-butadiene very readily polymerize free radically. The important thing to remember here is that there are double bonds still present in the polymer. This is especially important in the case of elastomers (synthetic rubbers) because some cross-linking with disulfide bridges (vulcanization) can occur in the finished polymer at the allylic sites still present to provide elastic properties to the overall polymers. Vulcanization will be discussed in detail in Chapter 18, Section 3. The mechanism shown in Fig. 14.3 demonstrates only the 1,4-addition of butadiene for simplicity. 1,2-Addition also occurs, and the double bonds may be cis or trans in their stereochemistry. Only with the metal complex... 

Oxidative Addition of Alkyl Halides to Palladium(0). The stereochemistry of the oxidative addition (31) of alkyl halides to the transition metals of group VIII can provide information as to which of the many possible mechanisms are operative. The addition of alkyl halides to d8-iridium complexes has been reported to proceed with retention (32), inversion (33), and racemization (34, 35) via a free radical mechanism at the asymmetric carbon center. The kinetics of this reaction are consistent with nucleophilic displacement by iridium on carbon (36). Oxi-... 

Sibi and Chen [42] reported a related tandem intermolecular nucleophilic free-radical addition-trapping reaction of enoate 168 establishing chirality at both a and /(-centers with control over both absolute and relative stereochemistry (Scheme 9.30) using a Lewis acid catalyst and the bisoxazoline ligand 169. They observed... 

In germanium chemistry the importance of free radical pathways in substitution reactions of secondary bromides with R3GeLi (R = CH3, CgHs) reagents is strongly indicated by product stereochemistry in cyclohexyl systems and by cyclization of the cA-heptene-2-yl moiety to yield [(2-methylcyclopentenyl)methyl]germanes, with the appropriate cis/trans ratio, as shown in equation 180, Table 9 and equations 181 and 182189. 

Stannyl- (and -silyl-) carboxylic acids undergo oxidative decarboxylation with LTA under mild conditions to provide the corresponding alkenes. This represents an improvement on the well-known alkene-forming decarboxylation of acids with LTA, which requires thermtd or photochemical conditions, for example. The directing metal effect leads to improved yields and regioselectivity. However, stereo-specific alkene formation did not occur and this could imply free radical involvement or transmetallation (Pb for Sn) (stereochemistry ) followed by cation formation, see for example Scheme 27. 

Finally, the ability of a tetracoordinate phosphorus compound to undergo electron capture and so provide free radicals has been linked with the stereochemistry of the substance ... 

From the data in Table 20, four important points should be kept in mind. First, free radical reduction of 139 and 137 with all reducing agents, as well as the tin hydride reduction of 138 and 140, occurred with the expected loss of stereochemistry. Second, the ratio of exo-/endo-norbomane-2-D obtained from these reductions was independent of the stereochemistry of starting material. Third, almost identical ratios of exo-/ ndo-norbornane-2-D were obtained from the four starting materials. Finally, the ratio of exo-(endo-norbornane-2-D was independent of the nature of the metal. 

Free radical reactions proceed under essentially neutral conditions that are compatible with various functional and protective groups used for saccharides. C-Glycosylation by means of radical reaction has been extensively developed [63]. This section will discuss intermolecular and intramolecular reactions for control of the stereochemistry of the C-glycoside linkage. 

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