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Thymine/triazine

Scheme 1 Thymine/triazine and Hamilton receptor/barbituric acid interactions with association constants of 800 and 3 x 10 respectively [42]... Scheme 1 Thymine/triazine and Hamilton receptor/barbituric acid interactions with association constants of 800 and 3 x 10 respectively [42]...
Resting cells, or extracts, of Streptococcus faecalis rapidly degrade th3uni-dine to thymine, and 2-deoxy-D-erythro-pentose ( 2-deoxy-D-ribose ) disappears. Azathymine [6-methyl-os2/m-triazine-3,5(2,4)-dione] or 5-bro-mouracil, when added, inhibits the disappearance of 2-deoxy-D-ri-bose by trapping it. Azathymidine can be isolated in gram quantities by this procedure. A 2-deoxy-D-ribofuranosyl derivative of 5-fluorouracil has been prepared in a similar way. ... [Pg.226]

Preparation of 1-A-Benzyl Thymine-3-[2-(l-A-t-Butoxy Carbonyl Etbylenediamine)]-5-Cbloro-s-Triazine... [Pg.415]

Binder et al. [92,93] have reported on the formation of poly(etherketone) poly(isobutylene) networks formed by the respective endgroup-modified telechelics. The relevant interactions investigated relied on the 2,6-diamino-1,3,5-triazine/thymine and the much weaker cytosine/2,6-diamino-1,3,5-triazine-modified polymers (Fig. 18). In addition to the pure hydrogenbonding interaction, phase-separation energies resulting from the strongly microphase separating PEK- and PIB polymers were expected. The association behavior was followed in solution via NMR-association experiments. [Pg.21]

Fig. 21 Assembly of polymers via triple-hydrogen bonds, a Formula of the flavine/2,6-diamino-triazine and thymine/2,6-diaminotriazine interactions, b Formation of nanopar-ticles/polymer aggregates, c Polymersome formation by aggregation of poly(norbornenes) and poly(styrenes) bearing N-bisacyl-2,6-diamino-pyridine and thymine side-chains, respectively. Reprinted with permission from [104,105]... Fig. 21 Assembly of polymers via triple-hydrogen bonds, a Formula of the flavine/2,6-diamino-triazine and thymine/2,6-diaminotriazine interactions, b Formation of nanopar-ticles/polymer aggregates, c Polymersome formation by aggregation of poly(norbornenes) and poly(styrenes) bearing N-bisacyl-2,6-diamino-pyridine and thymine side-chains, respectively. Reprinted with permission from [104,105]...
Synthesis of 4(6)-amino-l,3,5-triazine-2-ones and 2-thiones starting from benzotriazole derivatives has been reported <01JOC6797>. The first template photochemical synthesis of a 1,3,5-triazine derivative as a receptor capable of differentiating between thymine and uracil has been described <01CC1446>. A new solid phase synthesis of trisubslituted 6-amino(substituted)-2,4-dioxo-3,4-dihydro-l,3,5-triazines from a resin-bound amine component has been reported <01JCO278>. The synthesis of thirteen lris(azol-l-yl)-13,5-triazines, as a new class of multidentatc ligands, has been described <01H(55)905>. Tris(pyrazolyl-13,5-triazincs) 14 have been prepared by cyclotrimerization of aromatic nitriles, in piperidine and in solvent-free conditions <01T4397>. [Pg.312]

As a result, we prepare strong multiple hydrogen-bonding interactions between the 2,4-diaminotriazine groups of the PVDAT units and the T groups of the poly(vinylbenzylthymine) (PVBT) units in blends of poly(2-vinyl-4,6-diamino-l,3,5-triazine-co-methyl methacrylafe) (PVDAT-co-PMMA) and poly(vinylbenzyl thymine-co-methyl methacrylate) (PVBT-co-PMMA) as shown in Figure 2.13 [91]. [Pg.42]

Fig. 2 Classification of supramolecular building blocks functionalized with hydrogen-bonding groups (HBGs) and a few examples of self-complementary and heterocomplementary binding motifs. BTA benzene-1,3,5-tricarboxyamide, UPy ureidopyrimidinone, DATdiamino triazine. Thy thymine, Napy 2,7-diaminonaphtyriine, Ba barbituric acid, HR hamilton receptor... Fig. 2 Classification of supramolecular building blocks functionalized with hydrogen-bonding groups (HBGs) and a few examples of self-complementary and heterocomplementary binding motifs. BTA benzene-1,3,5-tricarboxyamide, UPy ureidopyrimidinone, DATdiamino triazine. Thy thymine, Napy 2,7-diaminonaphtyriine, Ba barbituric acid, HR hamilton receptor...
Many supramolecular polymers are derived directly from DNA s nucleobases adenine (A), cytosine (C), guanine (G), and thymine (T) [9]. Although each nucleobase can homodimerize, as described in the previous section, heterodynamic complexation is favored to different degrees. The G-C complex involves three H-bonds, and it is two or three orders of magnitude more stable than the A-T complex, involving only two H-bonds. 2,6-Diamino triazine derivatives strongly associate with thymine, and this pair has formed the basis for many studies. [Pg.52]

Butyl methacrylate-c< -vinylbenzyl thymine Styrene-c< -2-vinyl-4,6-diamino- 1,3,5-triazine Single Tg, FTIR I had <93 mol% butyl methacrylate II had <93 mol% styrene Kuo and Hsu (2010)... [Pg.1949]


See other pages where Thymine/triazine is mentioned: [Pg.122]    [Pg.1079]    [Pg.122]    [Pg.1079]    [Pg.149]    [Pg.23]    [Pg.187]    [Pg.331]    [Pg.39]    [Pg.607]    [Pg.547]    [Pg.1306]    [Pg.2652]    [Pg.629]    [Pg.142]    [Pg.80]    [Pg.243]   
See also in sourсe #XX -- [ Pg.123 ]




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