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Carboxylic amines

In turn the oxazoline-containing polymer may then react very rapidly (e.g. at 240°C) with such groups as carboxyls, amines, phenols, anhydrides or epoxides, which may be present in other polymers. This reaction will link the two polymers by a rearrangement reaction similar to that involved in a rearrangement polymerisation without the evolution of water or any gaseous condensation products (Figure 7.14). [Pg.156]

The functional groups that typically participate in this type of polymerization are carboxyl, amine, and alcohol groups. Examples of step growth polymers include polyesters and nylons, which are often spun into fibers used to manufacture carpeting and fabrics, and polycarbonates, which are converted into compact discs, jewel cases, and the large bottles used in water coolers. [Pg.50]

The following protocols may be used to create carboxyl-, amine-, or hydrazide-containing derivatives of dextran. [Pg.956]

Copolymers of ethyl acrylate with methacrylate and small amounts of hydroxyl, carboxyl, amine, or amide comonomers are used to prepare high quality latex points for wood, wall board and masonry in homes. [Pg.42]

Finally, the alcoholysis (RSiOH + HSiR ) catalyzed by metal carboxylate, amine or quaternary ammonium was patented by Gornowicz [149]. Various thermoplastics such as PA, PP, SBS and PE were described in the different examples. [Pg.138]

Intermolecular Nucleophilic Substitution with Heteroatom Nucleophiles. A patent issued in 1965 claims substitution for fluoride on fluorobenzene-Cr(CO)3 in dimethyl sulfoxide (DMSO) by a long list of nucleophiles including alkoxides (from simple alcohols, cholesterol, ethylene glycol, pinacol, and dihydroxyacetone), carboxylates, amines, and carbanions (from triphenyhnethane, indene, cyclohexanone, acetone, cyclopentadiene, phenylacetylene, acetic acid, and propiolic acid). In the reaction of methoxide with halobenzene-Cr(CO)3, the fluorobenzene complex is ca. 2000 times more reactive than the chlorobenzene complex. The difference is taken as evidence for a rate-limiting attack on the arene ligand followed by fast loss of halide the concentration of the cyclohexadienyl anion complex does not build up. In the reaction of fluorobenzene-Cr(CO)3 with amine nucleophiles, the coordinated aniline product appears rapidly at 25 °C, and a carefiil mechanistic study suggests that the loss of halide is now rate limiting. [Pg.3314]

M.Y. Galperin and E.V. Koonin. 1997. A diverse superfamily of enzymes with ATP-dependent carboxylate-amine/thiol ligase activity Protein Sci. 6 2639-2643. (PubMed)... [Pg.1059]

Pyridine-2-carboxylic amines, acids, phenols, diols, etc. 408 135 211... [Pg.469]

Noh Ncooh Nnh2 Nc=o Noch3 Nsh Nh2c= Nbenz - ) whose entries represent the number of oxhydryl, carboxylic, aminic, carbonylic, meth-oxy, thio, methylene, and phenyl functional groups, respectively. [Pg.92]

Ualporin, M. V.. and Koonin, li. V. 1907. A diverse superfamily of enzymes with A l H dependent carboxylate-amine/thiol lipase activity. Protein Set. 6 2639 2643. [Pg.729]


See other pages where Carboxylic amines is mentioned: [Pg.860]    [Pg.877]    [Pg.877]    [Pg.307]    [Pg.119]    [Pg.954]    [Pg.275]    [Pg.32]    [Pg.6]    [Pg.867]    [Pg.884]    [Pg.1147]    [Pg.522]    [Pg.643]    [Pg.55]    [Pg.169]    [Pg.172]    [Pg.32]    [Pg.149]    [Pg.4973]    [Pg.5663]    [Pg.532]    [Pg.277]    [Pg.120]    [Pg.2035]    [Pg.506]    [Pg.265]    [Pg.280]    [Pg.56]    [Pg.211]    [Pg.111]    [Pg.475]    [Pg.176]    [Pg.804]    [Pg.821]    [Pg.397]   
See also in sourсe #XX -- [ Pg.395 ]




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1.1.1- Trifluorides amines carboxylic acids

AMINES FROM MIXED CARBOXYLIC-CARBONIC ANHYDRIDES

Acetylene and Substituted Acetylenes in Presence of Carboxylic Acids, Hydrogen Halides, Mercaptans or Amines

Aminations carboxylic acids, pyridine

Amine and Carboxylic Ester

Amine from carboxylic acids

Amine reaction with carboxylic acids

Amine with carboxylic acids

Amines carboxylates

Amines carboxylates

Amines carboxylation

Amines carboxylation

Amines carboxylic acid amides

Amines carboxylic acid esters

Amines carboxylic acid reduction

Amines carboxylic acid thioamides

Amines carboxylic acids

Amines carboxylic acids and

Amines condensations, carboxylic acids, pyridine

Amines dehydrative condensations with carboxylic acids

Amines from carboxylic acid derivatives

Amines reaction with carboxylic

Amines salts formed between carboxylic acids

Amines synthesis from carboxylic

Amines with carboxylic acid anhydrides

Amines, separation from carboxylic acids

Aziridine-2-carboxylate ester amine

Carboxyl group conjugation amines

Carboxylation of amines

Carboxylic Acids, Esters, Amines, and Amides

Carboxylic acid anhydrides with ammonia and amines

Carboxylic acid azides amines

Carboxylic acid derivatives reaction with amine nucleophiles

Carboxylic acid hydrazides amines

Carboxylic acid hydrazides amines, Curtius

Carboxylic acid silyl esters amines

Carboxylic acids amine synthesis

Carboxylic acids from amine-catalyzed condensation reactions

Carboxylic acids reductive amination

Carboxylic amination

Carboxylic esters with amines

Condensations amines with carboxylic acids, pyridine

How Do Carboxylic Acid Derivatives React with Ammonia and Amines

Ketene aminals carboxylic acid chlorides

Olefins and Functional Derivatives in the Presence of Carboxylic Acids, Thiols, Amines or Hydrogen Chloride

Oxidation, amines carboxylic acids

Primary amines with carboxylic acid salts

Reducible Functional Groups Reductive Amination with Carboxylic Acids

Reductions of Carboxylic Acid Derivatives to Alcohols or Amines

Schmidt amines from carboxylic

Sulfonic or Carboxylic Acid-Amine Bifunctional Catalyst

Synthesis of Amines from Carboxylic Amides

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