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C-Branched

Diesters have been produced primarily by esterification of a C -branched-chain alcohol with adipic (C ), a2elaic (C ), or sebacic (C q) diacid. Di(2-ethylhexyl)sebacate [122-62-3] was quite generally used in military greases and MIL-L-7808 jet engine oil, but more recent demands and price competition have led to use of a variety of diesters. [Pg.245]

Fig. 1. Schematic diagram of polymer stmctures (a) linear (b) cross-linked and (c) branched, where LDPE — low density polyethylene and... Fig. 1. Schematic diagram of polymer stmctures (a) linear (b) cross-linked and (c) branched, where LDPE — low density polyethylene and...
Fig. 1. Examples of stmctures for silicates (a) monomer where is present (b) metasilicates where is present and (c) branched-ring... Fig. 1. Examples of stmctures for silicates (a) monomer where is present (b) metasilicates where is present and (c) branched-ring...
Synthesis of 3 -C- and 4 -C-branched oligodeoxynucleotides and the development of locked nucleic acids (LNA) 99ACR301. [Pg.262]

Another interesting effect seen in alkanes is that increased branching lowers an alkane s boiling point. Thus, pentane has no branches and boils at 36.1 3C, isopentane (2-methylbutane) has one branch and boils at 27.85 °C, and neopentane (2,2-dimethylpropane) has two branches and boils at 9.5 °C. Similarly, octane boils at 125.7 °C, whereas isooctane (2,2,4-trimethylpentane) boils at 99.3 °C. Branched-chain alkanes are lower-boiling because they are more nearly spherical than straight-chain alkanes, have smaller surface areas, and consequently have smaller dispersion forces. [Pg.92]

Figure 7.2 Three main types of homopolysaccharides, a) Single linkage type, eg curdlan. b) Side chain type, eg scleroglycan. c) Branched chain type, eg dextran. The figure also show various ways of illustrating exopolysaccharida structure. Figure 7.2 Three main types of homopolysaccharides, a) Single linkage type, eg curdlan. b) Side chain type, eg scleroglycan. c) Branched chain type, eg dextran. The figure also show various ways of illustrating exopolysaccharida structure.
Sacher F, Ehmann F, Gabriel S, Graf C, Branch FU (2008) Pharmaceutical residues in the river Rhine-results of one-decade monitoring programme. J Environ Monit 10(5) 664-670... [Pg.228]

C-branched sugars or C-oligosaccharides are obtainable through indium-promoted Barbier-type allylations in aqueous media.151 Indium-mediated allylation of a-chlorocarbonyl compounds with various allyl bromides in aqueous media gave the corresponding homoallylic chlorohydrins, which could be transformed into the corresponding epoxides in the presence of a base (Eq. 8.62).152... [Pg.248]

Figure 7. Polar plots of the reaction product vector for three surface mechanisms. Key a, simple adsorption-desorption b, series process, kt = kd = k and c, branch... Figure 7. Polar plots of the reaction product vector for three surface mechanisms. Key a, simple adsorption-desorption b, series process, kt = kd = k and c, branch...
A We show only the C atoms and the bonds between them. Remember that there are four bonds to each C atom the remaining bonds not shown are to H atoms. First we realize there is only one isomer with all six C atoms in one line. Then we draw the isomers with one 1-C branch. These are the center two structures below. The isomers with two 1-C... [Pg.619]

Allergy and Environmental Health Association-B.C. Branch Box 30033 Saanich Centre PO Victoria, BC V8X 5E1 Message phone 250-658-2027... [Pg.281]

Some common relationships between /Farches and their amino acid sequences are as follows (i) although the interior positions of the /Fstrands are mainly occupied by apolar (often C -branched) residues, the 2B1... [Pg.79]

M. Nomura, S. Shuto, M. Tanaka, T. Sasaki, S. Mori, S. Shigeta, and A. Matsuda, Nucleosides and Nucleotides. 185. Synthesis and biological activities of 4 -a-C-branched-chain sugar pyrimidine nucleosides, J. Med. Chem., 42 (1999) 2901-2908. [Pg.185]

On their side, Yin and Linker [216] made use of a 2-C-branched hexopyranoside, the synthesis of which was achieved by addition of dimethyl malonate to tri-O-benzyl-D-glucal (TUPAC name 3,4,6-tri-0-benzyl-l,5-anhydro-2-deoxy-D-araZtino-hex-l-enitol, Scheme 45) [217], Thus, saponification of the 2-C-[bis(meth-oxycarbonyl)]methyl derivative 184 to the corresponding malonic acid 185 was followed by heating in refluxing toluene. This led to decarboxylation and lactoniza-tion giving 186. The method was optimized and applied to the synthesis of pentoses and disaccharides. [Pg.53]

A pentopyranoside-fused butenolide is the key intermediate for the synthesis of the natural micotoxin patulin [226, 227]. Its synthesis involves Wittig olefination of a 3,4-di-O-protected arabinopyran-2-uloside, followed by protecting group removal and dehydration (Scheme 47). In other research, the glucopyranosid-2-uloside 190 was converted into the butenolide derivative 191 by aldol condensation with diethyl malonate and transesterification [228]. The latter was shown to be prone to autoxi-dation, leading to 192. Subsequent Michael addition with hydroxide ion, followed by decarboxylation, furnishes C-branched-chain sugar 193. [Pg.54]

Scheme 47 Synthesis of a 2-C-branched-chain sugar via a pyranose-fused butenolide... Scheme 47 Synthesis of a 2-C-branched-chain sugar via a pyranose-fused butenolide...
The above strain off, microcladia is biochemically different from all other seaweeds in nominally the same genus that have been examined so fer. It is also amazing that, after a decade since their first report, the rogiolenynes remain the sole examples of C-branched C, metabolites, in spite of the huge variety of compounds in this class, isolated on a world basis from seaweeds in the genus Laurencia and opisthobranch mollusks that feed on them. [Pg.53]

Polyacetylene alcohols Mar. cosmop. Nepheliosp., Haplosclerida, and Lithistida, Porif Land Umbelliferae, Ang. Ohta 1999, Fu 1999 non-terminal C-branched class in PcHif Guerriero 1998. [Pg.77]


See other pages where C-Branched is mentioned: [Pg.490]    [Pg.136]    [Pg.33]    [Pg.275]    [Pg.4]    [Pg.4]    [Pg.793]    [Pg.282]    [Pg.855]    [Pg.261]    [Pg.61]    [Pg.16]    [Pg.85]    [Pg.436]    [Pg.102]    [Pg.179]    [Pg.135]    [Pg.59]    [Pg.1212]    [Pg.138]    [Pg.40]    [Pg.42]    [Pg.50]    [Pg.51]    [Pg.54]    [Pg.112]    [Pg.53]    [Pg.79]   


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