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Starch tosylation

Deoxyfluorostarches were prepared from com starch by treatment of the tosylated (mostly at 0-6 of the o-glucosyl residues) starch precursors with KF in ethylene glycol (190°, 15 min) or by treatment of starch with hydrofluoric acid (Mc2SO, —30°, 4 h — room temp., 10 min). [Pg.222]

Poly(amino acids)2892 and polypeptides2893 can also be grafted onto starch. Starch was first alkylated in the presence of lithium naphthalene, and then the alkoxy derivatives were reacted with /V-carboxy anhydrides. Poly(amide amines) were produced by reacting amines with dioic acids on starch and then crosslinking with epichlorohydrin or 1,2-dichloroethane 2894 Grafting of starch with a synthetic polymer chain, for instance, polystyryl carboxylate anions prepared by an anionic polymerization, can be carried out on a blend of starch and cellulose functionalized by sulfonation, mesylation, or tosylation. In this manner, cellulose-starch graft copolymers were prepared.2895... [Pg.302]

Abstract Pure, well soluble p-toluenesulfwiyl (tosyl) starch samples with a DSm range... [Pg.205]

Synthesis of /Htoluenesulfonyl (tosyl) starch, and tosyl starch acetate... [Pg.208]

For a typical preparation, to a stirred solution of tosyl starch (1.0 g, DStos = 1.02) in 20 ml pyridine 0.3 g A iV-dimethylaminopyridine (DMAP) and 10 ml (106.0 mmol) acetic anhydride were added. The mixture was kept at 20°C for20 h and at 80 °C for 5 h. After cooling down to room temperature, the product was isolated by precipitation in 150 ml ethanol, filtered off, washed with ethanol and dried at 50 C under vacutun. [Pg.208]

Reaction of tosyl starch and tosyl starch acetate viith iodine... [Pg.208]

In order to guarantee an even distribution of the functional groups within the polymer chain, a homogeneous procedure for the tosylation reaction was preferred. It was already shown that homogeneous tosylation using the well-known starch solvent dimethyl sulfoxide does not yield products of sufficient degree of substitution . Therefore, we carried out the reaction in the solvent system A,iV-dimethyl acetamide (DMA)/LiCl which is usually applied for homogeneous functionalisation of cellulose. [Pg.209]


See other pages where Starch tosylation is mentioned: [Pg.125]    [Pg.279]    [Pg.302]    [Pg.279]    [Pg.206]    [Pg.215]    [Pg.125]    [Pg.279]    [Pg.302]    [Pg.279]    [Pg.206]    [Pg.215]    [Pg.23]    [Pg.30]    [Pg.116]    [Pg.123]    [Pg.148]    [Pg.193]    [Pg.197]    [Pg.212]    [Pg.213]    [Pg.16]    [Pg.372]    [Pg.89]    [Pg.224]    [Pg.302]    [Pg.28]    [Pg.1463]    [Pg.8]    [Pg.251]    [Pg.253]    [Pg.270]    [Pg.271]    [Pg.271]    [Pg.289]    [Pg.302]    [Pg.205]    [Pg.207]    [Pg.208]    [Pg.208]    [Pg.208]    [Pg.208]    [Pg.209]   
See also in sourсe #XX -- [ Pg.123 ]




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Starch tosylate

Tosyl starch

Tosyl starch acetate

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