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Core synthesis

Hirsch, A., Lamparth, I., and Grdsscr, T. (1994) Regiochemistry of multiple additions to the fullerene core Synthesis of a T -symmetric hexakisadduct of Ca with bis(ethoxycarbonyl)methylene. J. Am. Chem. Soc. 116, 9385-9386. [Pg.1073]

Unimolecular cyclizations involving C-N bond formation include intramolecular alkylations and acylations were applied for a variety of azocines, while macrocyclic O-alkylations and ketalizations are the most reliable methods for oxocine core synthesis through C-O bond formation. Other types of unimolecular cyclizations are scarce and erratic, and they usually depend on stereochemistry of the open-chain precursors and require tuning of the functional groups involved. [Pg.512]

Star-shape Poly(vinylmethyl-co-dimethyl)siloxanes with Carbosilane Core - Synthesis and Application... [Pg.99]

Shen, L., Shi, M., Li, F.Y., et al. (2006) Polyaryl ether dendrimer with a 4-phenylacetyl-5-pyrazolone-based terbium(III) complex as core synthesis and photophysical properties. Inorganic Chemistry, 45, 6188-6197. [Pg.90]

Core 1, the most common mucin-type O-linked core structure, is formed by the action of fSl-3 galactosyltransferase (fS3GalT), which adds galactose to form Galfi 1-3GalNAc (Fig. 2a). fS3GalT is expressed in most mammalian cells. The substrate specificity of this enzyme, like others involved in O-hnked core synthesis, is influenced by the amino acid sequences of substrate proteins and their glycosylation patterns. [Pg.638]

Wang, Y. Zeng, E. Zimmerman, S.C. Dendrimers with anthyridine-based hydrogen-bonding units at their cores synthesis, complexation and self-assembly studies. Tetrahedron Lett. 1997, 38, 5459-5462. [Pg.887]

For the maleimido activated core synthesis, the substitution of the resin does not have to be lower than 0.25 mmol/g. A normal substitution between 0.5 and -0.8 mmol/g will suffice the synthesis. [Pg.319]

H. Kang, J. Zubieta, Coordination complexes of polyoxomolybdates with a hexanuclear core synthesis... [Pg.137]

When D-mannosyl-L-rhamnosyl-D-galactosyl-PP-ACL is produced, the trisaccharide units rapidly polymerize to form O side-chain polysaccharide. If cell envelopes from strains unable to synthesize the core are utilized, the polysaccharide is not transferred to the core, and presumably stays attached to P-ACL. This conclusion was based on the observation that the polysaccharide could be extracted only after mild, acid hydrolysis and that a phosphate group was present at the reducing end of the polysaccharide thus obtained. In mutants defective in core synthesis, O side-chains were, indeed, found to accumulate, presumably in a form still linked to P-ACL. ... [Pg.420]

W. Yuan, et al.. Asymmetric penta-armed poly(e-caprolactone)s with short-chain phosphazene core synthesis, characterization, and in vitro degradation, Polym. Int. 54 (9) (2005) 1262-1267. [Pg.205]

Synthesis of tetrahydroimidazo[2,l-a]isoquinolines is another example of the reaction s utility in a fused core synthesis. Formation of compounds of structure 57 starts with 7-phenyl-5,6,7,8-tetrahydroiso-quinoline (56) amination in either DMA or tetralin in autoclave at 220 C for 18 h, which gives 53 in 41-48% yield, consecutively, although a higher yield is achieved when heating the starting material in DMA in the microwave for 12 h, which gives 58 in a 59% yield. The product is then used to construct the tetrahydroimidazo[2,l-a]isoquinoline framework using chloroacetone or 3-bromobutanone, which affords 58a,b in 46% and 75% yields, respectively... [Pg.550]

Goswami, A., and Singh, A. K., Hyperbranched polyester having nitrogen core synthesis and applications as metal ion extractant Reactive Functional Polymers, 61 255-263 (2004). [Pg.51]

Sankar J, Rath H, Prabhuraja V, Gokulnath S, Chandrashekar TK, Purohit CS, Verma S (2007) meso-meso-linked corrole dimers with modified cores synthesis, characterization, and properties. Chem Eur J 13 105-114... [Pg.432]

Hercules peifoims the dirty work such as parsing HardwareC and cleaning stables. His wife, Hebe, performs the core synthesis tasks such as scheduling and binding, and also serves wine to the gods on Mount Olympus. [Pg.8]

P3-Glucuronyl P3-GlcA to Gal 3 Involved in HNK-1 epitope and proteoglycan core synthesis... [Pg.610]


See other pages where Core synthesis is mentioned: [Pg.551]    [Pg.280]    [Pg.246]    [Pg.602]    [Pg.890]    [Pg.310]    [Pg.22]    [Pg.551]    [Pg.413]    [Pg.418]    [Pg.421]    [Pg.273]    [Pg.219]    [Pg.242]    [Pg.563]    [Pg.248]    [Pg.334]   
See also in sourсe #XX -- [ Pg.88 ]

See also in sourсe #XX -- [ Pg.88 ]




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Core-first star synthesis

Core-first star synthesis compounds

Core-first star synthesis polymerization

Core-first star synthesis precursors

Core-shell nanocable synthesis

Core-shell synthesis

Cored dendrimer, synthesis

Endoplasmic reticulum core protein synthesis

Golgi apparatus core protein synthesis

Roseophilin core, synthesis

Spirocyclic core synthesis

Synthesis of Core

Synthesis of Core-Shell Nanocrystals with InAs Cores

Synthesis of O-Glycan Core

Tetracyclic core synthesis

Total synthesis indole core and side-chain modifications

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