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Acid proliferation reactions

Acid Proliferation Reactions and Their Application to Chemically Amplified Lithographic Imaging... [Pg.161]

Ketal Tosylates. The second candidate for the acid proliferation is ketal derivatives having a tosylated residue (5). These were synthesized by the ketalization of benzoylacetate, followed by LAH reduction and tosylation (5). Compound 5 (mp 48-50 C) had to be stored in a refrigerator since crystals of 5 were converted into black materials gradually at an ambient temperature upon prolonged storage. The ketal compound (5) was readily converted in the present of an addic spedes into p-keto-tosylate (6) which is subjected to the -elimination to give TsOH in a non-linear maimer (Scheme 2(b)). NMR spectra of a solution of 5 in the presence of TsCH at 100 revealed that e p-keto-tosylate (6) as an intermediate was formed during the reaction (6). [Pg.164]

One of the most important types of chemical reactions is the acid-base reaction. However, the definition of which species constitute acids or bases has evolved over the years as the breadth of known chemical reactions has continued to proliferate. For this reason, it is necessary to first introduce the more common historical definitions of acids and bases so that we may better understand how they each fit into the lexicon of chemical reactivity. Just as there were several complimentary models to facilitate our understanding of chemical bonding, so too there are numerous definitions of what it means to be an acid or a base. Which of these definitions we choose will depend on the complexity of the specific acid-base interaction at hand. Ultimately, however, every acid-base reaction entails a change in the way that the valence electrons are arranged in the atomic or molecular orbitals of the participating species. Therefore, the most modem definition of acid-base chemistry builds upon the MO concepts developed in previous chapters and provides the context for a natural continuation of that discussion. [Pg.455]

The successful use of [ F]FDG in oncology PET imaging has prompted the design of several other radiopharmaceuticals, such as [ F]FLT ([ F]fluorothymi-dine, used as cellular proliferation marker. Scheme 36) [152-154], F-MISO ([ F] fluoromisonidazole, used to assess tissue hypoxia. Scheme 37) [155], c/s-4-[ F] fluoro-L-proline (used as abnormal collagen synthesis marker. Scheme 38) [156] and 0-(2-[ F]fluoroethyl)-L-tyrosine (used as amino acid transport and/or protein synthesis marker. Scheme 39) [157]. All these fluorine-18-labelled molecules have been prepared by aliphatic nucleophilic fluorination followed by a deprotection reaction. [Pg.33]

It is a cyclic polypeptide with 11 amino acids. It selectively inhibits T-lymphocytes proliferation, IL-2 and other cytokine production. It is the most effective drug for prevention and treatment of graft rejection reaction. It is used in cardiac, hepatic, renal, bone marrow transplantation and as second line drug in rheumatoid arthritis, inflammatory bowel disease, dermato-myositis, bronchial asthma and certain other autoimmune diseases. [Pg.379]

It is also possible that the short chain fatty acids may affect the expression of the transcription factors NF-kB, which controls the expression of several genes involved in inflammatory and immunological reactions and cell proliferation. Butyric acid, for example, may inhibit the expression of NF-kB and this may be a beneficial influence on the relationship between dairy fat and CVDs (Reviewed in Bryngelsson, 2008). [Pg.20]

Cornwell DC, Morisaki N (1984), Fatty acid paradoxes in the control of cell proliferation prostaglandins, lipid peroxides and cooxidation reactions, In Pryor WA (Ed.), Free Radicals in Biology VI, Academic Press, New York, pp. 95-147. [Pg.106]


See other pages where Acid proliferation reactions is mentioned: [Pg.162]    [Pg.162]    [Pg.448]    [Pg.738]    [Pg.161]    [Pg.170]    [Pg.208]    [Pg.315]    [Pg.755]    [Pg.544]    [Pg.239]    [Pg.193]    [Pg.213]    [Pg.160]    [Pg.142]    [Pg.681]    [Pg.210]    [Pg.6]    [Pg.457]    [Pg.223]    [Pg.143]    [Pg.461]    [Pg.67]    [Pg.98]    [Pg.452]    [Pg.531]    [Pg.419]    [Pg.1204]    [Pg.74]    [Pg.21]    [Pg.147]    [Pg.205]    [Pg.197]    [Pg.198]    [Pg.292]    [Pg.512]   


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