Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Glycols solid support

Fused silica capillary columns of various internal bores and of lengths in the range 25 to 50 m are mainly employed for analytical separations. A variety of polar and non-polar column types are available including those open tubular types with simple wall coatings (WCOT), those with coatings dispersed on porous solid-supports to increase adsorbent surface area (SCOT) and porous layer open tubular (PLOT) columns. Important stationary phases include polyethylene glycol, dimethylpolysiloxane and different siloxane copolymers. Various sample introduction procedures are employed including ... [Pg.565]

Poly(ethylene glycol) supported liquid-phase syntheses by both the reaction of (polyethylene glycol (PEG))-supported imines with nitrile oxides, generated in situ from aldoximes, (300) and 1,3-dipolar cycloadditions of nitrile oxide, generated in situ on soluble polymers with a variety of imines (301, 302) have been described. The solid-phase synthesis of 1,2,4-oxadiazolines via cycloaddition of nitrile oxide generated in situ on solid support with imines has also been elaborated (303). These syntheses of 1,2,4-oxadiazolines provide a library of 1,2,4-oxadiazolines in good yields and purity. [Pg.46]

Soluble polyethylene glycol (PEG) as polymer support was also successfully investigated. Precipitation after each reaction step in order to remove excesses of reagents and soluble byproducts seemed to work well. Another topic of great interest is direct glycosylation of solid support connected peptides in order to arrive finally at glycopeptides. (9-Glycosyl trichloroacetimidates also proved successful in this endeavor. [Pg.97]

PEG has been converted into a solid support by grafting functionalized polyethylene glycol chains onto polystyrene to form constructs such as TentaGel ... [Pg.181]

Scheme 10.1 Glycopeptide synthesis and a-chymotrypsin catalyzed release from the solid support, a) 25% TFA (CH2CI2) b) 0-(N-Boc-Phe)glycolic acid (7 eq), BOP, HOBt, DIEA b) 25% TFA (CH2CI2) c) Boc-Gly-OH (7 eq), BOP, HOBt, DIEA c) 25% TFA (CH2CI2) d) Boc-Asn(GlcNAcb)-OH (3 eq), BOP, DIEA e) galactosyl transferase, sialyl transferase f) CT, H2O, pH 7.0 g) ultrafiltration h) a-l,3-fuco-syltransferase, GDP-Fuc (2.5 eq), 0.1 M HEPES (pH 7.0), 95%. Scheme 10.1 Glycopeptide synthesis and a-chymotrypsin catalyzed release from the solid support, a) 25% TFA (CH2CI2) b) 0-(N-Boc-Phe)glycolic acid (7 eq), BOP, HOBt, DIEA b) 25% TFA (CH2CI2) c) Boc-Gly-OH (7 eq), BOP, HOBt, DIEA c) 25% TFA (CH2CI2) d) Boc-Asn(GlcNAcb)-OH (3 eq), BOP, DIEA e) galactosyl transferase, sialyl transferase f) CT, H2O, pH 7.0 g) ultrafiltration h) a-l,3-fuco-syltransferase, GDP-Fuc (2.5 eq), 0.1 M HEPES (pH 7.0), 95%.
The Sharpless asymmetric dehydroxylation of resin-bound olefins was monitored using 3H, 13C and HMQC HRMAS NMR.63 The authors found 13C HRMAS NMR to be particularly suited to evaluating the progress of this reaction and permitted the enantiomeric excesses of the products to be determined before they were cleaved from the support. Most importantly, they were able to evaluate the types of substrates amenable to this reaction on solid supports, showing the ability of HRMAS NMR to contribute to synthetic questions. Transformation of the unnatural amino acid Lys(NH2) on a poly (ethylene glycol)-dimethylacrylamide (PEGA) resin to 6-hydroxynorleucine was confirmed by application of TOCSY HRMAS experiments.64... [Pg.273]

All peptide-catalyzed enone epoxidations described so far were performed using insoluble, statistically polymerized materials (neat or on solid supports). One can, on the other hand, envisage (i) generation of solubilized poly-amino acids by attachment to polyethylene glycols (PEG) and (ii) selective construction of amino acid oligomers by standard peptide synthesis-linked to a solid support, to a soluble PEG, or neat as a well-defined oligopeptide. Both approaches have been used. The former affords synthetically useful and soluble catalysts with the interesting feature that the materials can be kept in membrane reactors for continuously oper-... [Pg.296]

Fig. 2. Application of the polyethylene glycol-co-monomethyl ether (MPEG) solid support with an a,a -dioxyxylyl (DOX) diether linker for oligosaccharide synthesis in solution. Fig. 2. Application of the polyethylene glycol-co-monomethyl ether (MPEG) solid support with an a,a -dioxyxylyl (DOX) diether linker for oligosaccharide synthesis in solution.
Oxetanes have also been synthesized by the immobilization of 2,2 -disubstituted 1,3-diols with polymer-bound sulfonyl chloride, followed by intramolecular cyclization/cleavage from the solid support (Scheme 17) <2005TL643>. One percent divinylbenzene (DVB) cross-linked polystyrene and polyethylene glycol (PEG) (average Mn 3400) were used as polymer support in this reaction, and in both cases the properties of the polymer support allowed rapid purification of the intermediate. Intermediates on the insoluble cross-linked polystyrene support could be washed with a range of organic solvents to remove insoluble impurities, whereas the soluble PEG supported products could be purified by recrystallization from isopropanol. This is thought to represent the first reported polymer-supported synthesis of oxetanes. [Pg.344]

Various polymeric and solid supports, such as polyethylene glycol (PEG), can be used to immobilise these catalysts.[46 48] Exchanging the polymer support on the styrene moiety for charged ionic liquid tags affords complexes 38 and 39, which are retained to a significantly higher degree in the ionic liquid phase (Scheme 7.4). [Pg.162]

One major disadvantage of the OBOC method using the on-bead screening method is that each library compound is tethered to the solid support via a linker such as polyethylene glycol and may result in steric hindrance between the cellular receptor and the library compound. However, in some instances the linker may be beneficial, for example, the linker can be used as a convenient handle to link the cancer-targeting ligand to the therapeutic payload. [Pg.1431]


See other pages where Glycols solid support is mentioned: [Pg.131]    [Pg.148]    [Pg.185]    [Pg.139]    [Pg.135]    [Pg.501]    [Pg.138]    [Pg.206]    [Pg.288]    [Pg.144]    [Pg.78]    [Pg.78]    [Pg.484]    [Pg.169]    [Pg.157]    [Pg.539]    [Pg.76]    [Pg.13]    [Pg.231]    [Pg.300]    [Pg.348]    [Pg.43]    [Pg.385]    [Pg.391]    [Pg.253]    [Pg.365]    [Pg.437]    [Pg.194]    [Pg.37]    [Pg.116]    [Pg.75]    [Pg.231]    [Pg.682]    [Pg.299]    [Pg.78]    [Pg.202]    [Pg.44]    [Pg.622]   
See also in sourсe #XX -- [ Pg.841 , Pg.843 ]

See also in sourсe #XX -- [ Pg.841 , Pg.843 ]

See also in sourсe #XX -- [ Pg.841 , Pg.843 ]




SEARCH



Solid support

Solid-supported

© 2024 chempedia.info