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Thermal rearrangement, continuous

Earlier work on the photolytic or thermal rearrangement of polyhalogenated pyridazines to corresponding pyrazines has been continued,14,161,774,1690 but the fascinating results offer little of preparative value. It has been reported that 300-nm irradiation of 3,4,5,6-tetra-tert-butylpyridazine (66) gave a quantitative yield of the Dewar isomer (3,4,5,6-tetra-tert-butyl-l,2-diazabicyclo [2.2.0]hexa-2,5-diene 67] that subsequently afforded 2,3,5,6-tetra-tert-butylpyrazine (68) in 18% yield on 254-nm irradiation.1464... [Pg.57]

Figure 7 Continuous Pilot Plant Reactor for Thermal Rearrangement... Figure 7 Continuous Pilot Plant Reactor for Thermal Rearrangement...
The first general method of transforming a penicillin into a cephalosporin, the acid-catalysed rearrangement of penicillin sulphoxides, continues to receive attention. That this rearrangement proceeds via a sulphenic acid derivative has been further confirmed by isolation of the crystalline sulphenic acid (74 f, y) from the thermal rearrangement of the penicillin sulphoxide (27 f, y). This intermediate slowly reverts to the penicillin at 38 0, and, on treatment with methanesulphonic acid in dimethylacetamide, cyclizes to cephalosporin (75 f, y). Trapping of (74) by oxidation to the sulphinyl chloride (76 f, y) has been reported cyclization to a cephalosporin sulphoxide was accomplished under base catalysis/ Treatment of penicillin sulphoxides with azo-compounds also effects rearrangement to... [Pg.202]

It has been proposed that protonation or complex formation at the 2-nitrogen atom of 14 would enhance the polarization of the r,6 -7i system and facilitate the rearrangement leading to new C-C bond formation. The equilibrium between the arylhydrazone and its ene-hydrazine tautomer is continuously promoted to the right by the irreversible rearomatization in stage II of the process. The indolization of arylhydrazones on heating in the presence of (or absence of) solvent under non-catalytic conditions can be rationalized by the formation of the transient intermediate 14 (R = H). Under these thermal conditions, the equilibrium is continuously pushed to the right in favor of indole formation. Some commonly used catalysts in this process are summarized in Table 3.4.1. [Pg.118]

In this primer, Ian Fleming leads you in a more or less continuous narrative from the simple characteristics of pericyclic reactions to a reasonably full appreciation of their stereochemical idiosyncrasies. He introduces pericyclic reactions and divides them into their four classes in Chapter 1. In Chapter 2 he covers the main features of the most important class, cycloadditions—their scope, reactivity, and stereochemistry. In the heart of the book, in Chapter 3, he explains these features, using molecular orbital theory, but without the mathematics. He also introduces there the two Woodward-Hoffmann rules that will enable you to predict the stereochemical outcome for any pericyclic reaction, one rule for thermal reactions and its opposite for photochemical reactions. The remaining chapters use this theoretical framework to show how the rules work with the other three classes—electrocyclic reactions, sigmatropic rearrangements and group transfer reactions. By the end of the book, you will be able to recognize any pericyclic reaction, and predict with confidence whether it is allowed and with what stereochemistry. [Pg.92]

While there have been efforts to polymerize other surfactant mesophases and metastable phases, bicontinuous cubic phases have only very recently been the subject of polymerization work. Through the use of polymerizable surfactants, and aqueous monomers, in particular acrylamide, polymerization reactions have been performed in vesicles (4-8). surfactant foams ), inverted micellar solutions (10). hexagonal phase liquid crystals (111, and bicontinuous microemulsions (121. In the latter two cases rearrangement of the microstructure occured during polymerization, which in the case of bicontinuous microemulsions seems inevitable b ause microemulsions are of low viscosity and continually rearranging on the timescale of microseconds due to thermal disruption (131. In contrast, bicontinuous cubic phases are extremely viscous in genei, and although the components display self-diffusion rates comparable to those... [Pg.204]


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Rearrangement thermal

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