Relevant bibliographies by topics / D-Glucofuranose

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'D-Glucofuranose'

Author: Grafiati
Published: 5 June 2025
Last updated: 15 July 2025

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Journal articles on the topic "D-Glucofuranose"

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Hřebabecký, Hubert, Jan Dočkal та Antonín Holý. "Synthesis of Deoxy, Dideoxy and Didehydrodideoxy Analogs of 9-(β-D-Hexofuranosyl)adenine". Collection of Czechoslovak Chemical Communications 59, № 6 (1994): 1408–19. http://dx.doi.org/10.1135/cccc19941408.

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Condensation of 1,2-di-O-acetyl-3,5,6-tri-O-benzoyl-D-glucofuranose with N6-benzoyladenine, catalyzed with tin tetrachloride, afforded nucleoside I. Partial deacetylation of I, followed by mesylation, gave 9-(3,5,6-tri-O-benzoyl-2-O-methanesulfonyl-β-D-glucofuranosyl)adenine (III). 9-(2,5,6-Tri-O-acetyl-3-O-methanesulfonyl-β-D-glucofuranosyl)-N6-benzoyladenine (IV) was prepared by condensation of 1,2,5,6-tetra-O-acetyl-3-O-methanesulfonyl-D-glucofuranose with N6-benzoyladenine. Reaction of mesyl derivative III with methanolic sodium methoxide and of mesyl derivative IV with methanolic ammonia
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2

Svoboda, Jiří, Karel Čapek та Jaroslav Paleček. "Esters of arylpropionic acids with 1,2:5,6-di-O-isopropylidene- and 1,2-O-isopropylidene-α-D-glucofuranose". Collection of Czechoslovak Chemical Communications 52, № 3 (1987): 766–74. http://dx.doi.org/10.1135/cccc19870766.

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On fractional crystallization of 3-O-(2-(2-fluoro-4-biphenylyl)propionyl)-, 3-O-(2-(4-isobutylphenyl)propionyl)- and 3-O-(2-(6-methoxy-2-naphthyl)propionyl)-1,2 :5,6-di-O-isopropylidene-α-D-glucofuranoses V-VII optically pure R-diastereoisomers were isolated. The derivatives of 1,2-O-isopropylidene-α-D-glucofuranose obtained on partial deacetylation of esters V-VII were separated chromatographically to R and S-diastereoisomers. Their hydrolysis or transesterification afforded optically pure arylpropionic acids or their methyl esters, respectively. Kinetic resolution of the acids gives rise to
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3

Utkina, Natalia K., Natalia D. Pokhilo, and Lyubov N. Atopkina. "Antiradical Activity of Naphthazarin-Carbohydrate Nonglycoside Conjugates." Natural Product Communications 14, no. 5 (2019): 1934578X1984817. http://dx.doi.org/10.1177/1934578x19848170.

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The ABTS·+ scavenging activity of known (4, 6-8) and new (5, 9-12) naphthazarin-carbohydrate nonglycoside conjugates, and methoxynaphthazarins 1-3 was evaluated. The study of structure-activity relationships showed that the presence of carbohydrate fragments in the structure of naphthazarin-carbohydrate conjugates increased their antiradical activity compared with starting methoxynaphthazarins. Antiradical activity depends on the structure of carbohydrate fragments, their number, and position. Depending on the carbohydrate fragment the activity increased in the following order: methyl-α-d-gluc
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Nizamov, Ilyas S., Yevgeniy N. Nikitin, Ilnar D. Nizamov та ін. "α-d-Glucofuranose and α-d-allofuranose diacetonides and silyl ether of α-d-glucofuranose diacetonide in dithiophosphorylation reactions". Heteroatom Chemistry 27, № 6 (2016): 345–52. http://dx.doi.org/10.1002/hc.21344.

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5

Bujnicki, Bogdan, Jarosław Błaszczyk, Marek Chmielewski та Józef Drabowicz. "Diastereoisomerically Pure, (S)-O-1,2-O-isopropyli dene-(5-O-α-d-glucofuranosyl) t-butanesulfinate: Synthesis, Crystal Structure, Absolute Configuration and Reactivity". Molecules 25, № 15 (2020): 3392. http://dx.doi.org/10.3390/molecules25153392.

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The reaction of t-butylmagnesium chlorides with diastereomerically pure (R)-1,2-O-isopropylidene-3,5-O-sulfinyl-α-d-glucofuranose (R)-4 was found to be stopped at the stage of the corresponding, diastereoisomerically pure 1,2-O-isopropylidene-(5-O-α-d-glucofuranosyl) t-butanesulfinate (S)-10 for which the crystal structure and the (S)-absolute configuration was determined by X-ray crystallography. Comparison of the absolute configurations of the starting sulfite (R)-4, and t-butanesulfinate (S)-10 (which crystallizes in the orthorhombic system, space group P212121, with the single compound mol
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6

Erişkin, Selinay Y., Fatma Ç. Telli, Yeliz Yıldırım, and Yeşim Salman. "Synthesis, Characterization, and Thermokinetic Analysis of New Epoxy Sugar Derivative." Journal of Chemistry 2014 (2014): 1–6. http://dx.doi.org/10.1155/2014/737953.

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The synthesis of 5,6-O-isopropylidene-1,2-O-(R)-trichloroethylidene-α-D-glucofuranose (compound1) and 5,6-O-isopropylidene-1,2-O-(R)-trichloroethylidene-3-O-(2′,3′-epoxypropan-1′-yl)-α-D-glucofuranose (compound2) was carried out. The synthesized compounds1and2were characterized by nuclear magnetic resonance (1H-NMR), Fourier transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TG). The FTIR and1H NMR spectra showed that the epoxy group in compound2was attached by means of a nucleophilic substitution reaction. The activation energies for thermal degradation of compounds1and2w
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7

Chibac, Andreea L., Tinca Buruiana, Violeta Melinte, Ionel Mangalagiu, and Emil C. Buruiana. "Tuning the size and the photocatalytic performance of gold nanoparticles in situ generated in photopolymerizable glycomonomers." RSC Advances 5, no. 110 (2015): 90922–31. http://dx.doi.org/10.1039/c5ra14695j.

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Polymer nanocomposites containing Au NPs in situ photogenerated during the UV-curing process were prepared starting from methacrylated glycomonomers with α-d-glucofuranose or d-mannitol structural units, other mono(di)methacrylates and AuCl<sub>3</sub>.
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Dhudmal, Chaya N., Dhanraj O. Biradar, Maddipatla V. Satyanarayana, and Basi V. Subba Reddy. "Stereoselective Total Synthesis of 1,4-Dideoxy-1,4-imino-L-ribitol by an Intramolecular Ring Opening of Epoxide with a Tethered Amide." Natural Product Communications 13, no. 8 (2018): 1934578X1801300. http://dx.doi.org/10.1177/1934578x1801300821.

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Stereoselective total synthesis of 1,4-dideoxy-1,4-imino-L-ribitol has been accomplished from D-glucose. The key step involved in this synthesis is the regioselective ring-opening of the epoxide with a tethered amido group to give the N-tosyl-3,6-dideoxy-3,6-imino-1,2- O-isopropylidene-α-D-glucofuranose.
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9

Furneaux, Richard H., Bénédicte Martin, Phillip M. Rendle та Carol M. Taylor. "Glucofuranosylation with penta-O-propanoyl-β-d-glucofuranose". Carbohydrate Research 337, № 21-23 (2002): 1999–2004. http://dx.doi.org/10.1016/s0008-6215(02)00300-2.

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10

Morin, Christophe, та Lionel Ogier. "Synthesis of 5-O-β-Iodoethyl-D-Glucofuranose". Journal of Carbohydrate Chemistry 19, № 1 (2000): 111–17. http://dx.doi.org/10.1080/07328300008544068.

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Dissertations / Theses on the topic "D-Glucofuranose"

1

Wingert, Amanda E. "Atom Transfer Radical Polymerization (ATRP) of 3-O-Methacryloyl-1,2:5,6-di-O-Isopropylidene-D-Glucofuranose (MAIpGlc): Towards Sugar-Functionalized, Non-Ionic, Diblock Copolymer Brushes." University of Cincinnati / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1299005265.

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Book chapters on the topic "D-Glucofuranose"

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David, Serge. "Sugars in chiral synthesis." In The Molecular and Supramolecular Chemistry of Carbohydrates: Chemical Introduction to the Glycosciences. Oxford University PressOxford, 1997. http://dx.doi.org/10.1093/oso/9780198500476.003.0008.

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Abstract The experiments we are about to describe bring into play chiral reagents constructed from a titanocene (titanium-carbohydrate complex) (Riediker and Duthaler 1989a; Duthaler et al. 1989; Bold et al. 1989; Riediker et al. 1989b). The starting compound is cyclopentadienyltitanium(IV) trichloride, C5H5TiCl3, which is prepared from dichloride (C5H5)iTiC12 by heating with TiC14. This trichloride reacts with 1,2:5,6-di-0-isopropylidene-α-D-glucofuranose (‘diacetone glucose’) in the presence of triethylamine to provide the bis-titanate 8.1. The latter is a crystalline compound, hence its structure could be determined in the solid state. Its form is that of a three-legged piano stool with the cyclopentadiene ring being its seat. The two ligands have completely different orientations with respect to the cyclopentadienyl ring. Because of this, they create a chiral cavity around the titanium atom. A study of the NMR spectra of 8.1 in solution indicates neither inversion at the metal centre nor rapid ligand exchange. This suggests that the conformation in solution is close to the conformation in the crystal.
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2

"Diosmetin-7-O-β-D-glucofuranoside." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0535-1_434.

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3

"Isorhamnetin-7-O-α-L-rhamnofuranosyl-3-O-β-D-glucofuranosyl-6-O-β-D-glucopyranoside." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0535-1_517.

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You might also be interested in the extended bibliographies on the topic 'D-Glucofuranose' for particular source types:
Journal articles
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