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Synthesis formation

B. Giese Radicals in Organic Synthesis Formation of Carbon-Carbon Bonds (Pergamon Press NY) 1986 Bull. Soc. Chirn. Fr. 1990, 127,675 Tetrahedron 1981, 37, 3073 Tetrahedron 1987, 43, 3541 Advances in Free Radical Chemistry 1990, 1, 121. [Pg.144]

SENARY Conjugated Aldehyde Synthesis Formation ot polyunsaturated aldehydes trom vinyl halides and enamlnoaldehydes... [Pg.31]

EHRLICH - SACHS Aldehyde Synthesis Formation of o-nitrobenzaldehydes from o-nitrotoluenea. [Pg.103]

FORSTER Diazo Synthesis Formation ol diazo denvatives from oximes... [Pg.126]

K A L U Z A Isothiocyanate synthesis Formation of isothiocyanates from amines. [Pg.199]

LEUCKART Thiophenot Synthesis Formation of Ihiophenols from diazonium salts and xanthates... [Pg.231]

B. Giese, Radicab in Organic Synthesis Formation of Carbon-Carbon Bonds, Permagon Press, Oxford, U.K.,... [Pg.733]

The hindered carbon-centered radicals are most suited as mediators in the polymerization of 1,1-disubstituled monomers e.g. MMA,78,95 other methacrylates and MAA,06 and AMS97). Polymerizations of monosubstituted monomers are not thought to be living. Dead end polymerization is observed with S at polymerization temperatures <100°C.98 Monosubstituted monomers may be used in the second stage of AB block copolymer synthesis (formation of the B block).95 However the non-living nature of the polymerization limits the length of the B block that can be formed. Low dispersities are generally not achieved. [Pg.469]

For a summary of methods of radical formation, see Giese, B. Radicals in Organic Synthesis Formation of Carbon-Carbon Bonds Pergamon Elmsford, NY, 1986, p. 267. For a review on formation of free radicals by thermal cleavage, see Brown, R.F.C. Pyrolytic Methods in Organic Chemistry Academic Press NY, 1980, p. 44. [Pg.269]

Lian, J.B., Duan, X.C., Ma, J.M., Peng, P., Kim, T.I. and Zheng, W.J. (2009) Hematite (alpha-Fe2C>3) with various morphologies ionic liquid-assisted synthesis, formation mechanism, and properties. ACS Nano, 3 (11), 3749—3761. [Pg.83]

Since new carbonyl compounds of Ti, Zr, and Hf and their accompanying chemistry are appearing at a steady rate in the literature, it seems appropriate at this time to bring this rapidly growing area into perspective. In this review we will endeavor to categorize all reported group 4B metal carbonyls including their synthesis, formation,1 structure, spectroscopic... [Pg.318]

Giese B (1986) Radicals in Organic Synthesis. Formation of Carbon-Carbon Bonds. Pergamon, Oxford... [Pg.169]

Kariv-Miller E, Nanjundiah C, Eaton J, Swenson KE (1984) J. Electroanal. Chem. 167 141 Loffredo DM, Swartz JE, Kariv-Miller E (1989) J. Org. Chem. 54 5953 Giese B (1986) Radicals in organic synthesis formation of carbon-carbon bonds, 1st edn. Pergamon Press, Oxford... [Pg.47]

For reviews of chemical approaches to radical cyclization reactions see a) Motherwell WB, Crich D (1992) Free radical chain reactions in organic synthesis, Academic Press, London, b) Giese B (1986) Radicals in organic synthesis formation of carbon-carbon bonds, Pergamon, Oxford, and c) Jasperse CP, Curran DP, Fevig TL (1991) Chem Rev 91 1237... [Pg.85]

With the growing importance of modern combinatorial chemistry, additional benefits accrue for catalyst systems that readily adapt to 96 well or higher density synthesis formats. [Pg.468]

Insulin is a polypeptide hormone that consists of two peptide chains bonded by two disulfide bonds. The two chains are designated A and B. The A chain consists of 21 amino acids with a third internal disulfide bond, and the chain contains the remaining 30 amino acids. All vertebrates produce insulin and the structure is similar in these species. For example, the insulin produced in humans and porcine species differs by only one amino acid, and humans and bovine insulin differ by three amino acids. Insulin plays a crucial role in several physiological processes. These include the regulation of sugar in the body, fatty acid synthesis, formation of triglycerides, and amino acid synthesis. [Pg.156]

Pathway of porphyrin synthesis formation of poiphobilinogen. (Continued in Figure 21.4.)... [Pg.276]


See other pages where Synthesis formation is mentioned: [Pg.200]    [Pg.337]    [Pg.417]    [Pg.945]    [Pg.1097]    [Pg.114]    [Pg.228]    [Pg.449]    [Pg.152]    [Pg.180]    [Pg.215]    [Pg.69]    [Pg.44]    [Pg.18]    [Pg.677]    [Pg.744]    [Pg.169]    [Pg.273]   
See also in sourсe #XX -- [ Pg.51 , Pg.141 ]




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