Bibliografías temáticas / Furanoside / Artículos de revistas
Siga este enlace para ver otros tipos de publicaciones sobre el tema: Furanoside.

Artículos de revistas sobre el tema "Furanoside"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 16 de febrero de 2022

Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros

Elija tipo de fuente:

Consulte los 50 mejores artículos de revistas para su investigación sobre el tema "Furanoside".

Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.

También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.

Explore artículos de revistas sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.

1

Gerbst, Alexey G., Vadim B. Krylov, Dmitry A. Argunov, Maksim I. Petruk, Arsenii S. Solovev, Andrey S. Dmitrenok y Nikolay E. Nifantiev. "Influence of per-O-sulfation upon the conformational behaviour of common furanosides". Beilstein Journal of Organic Chemistry 15 (15 de marzo de 2019): 685–94. http://dx.doi.org/10.3762/bjoc.15.63.

Texto completo
Resumen
The studies on the recently discovered pyranoside-into-furanoside rearrangement have led us to conformational investigations of furanosides upon their total sulfation. Experimental NMR data showed that in some cases drastic changes of the ring conformation occurred while sometimes only the conformation of the exocyclic C4–C5 linkage changed. Herein we describe a combined quantum chemical and NMR conformational investigation of three common monosaccharide furanosides as their propyl glycosides: α-mannose, β-glucose and β-galactose. Full exploration of the furanoside ring by means of ab initio calculations was performed and coupling constants were calculated for each of the low-energy conformers. The results demonstrated preferred trans-orientation of H4–H5 protons in the non-sulfated molecules which changed to gauche-orientation upon sulfation. The effect is less pronounced in the galactosides. For all the studied structures changes in the conformational distribution were revealed by quantum mechanical calculations, that explained the observed changes in intraring coupling constants occurring upon introduction of sulfates.
Los estilos APA, Harvard, Vancouver, ISO, etc.
2

Sanapala, Someswara Rao y Suvarn S. Kulkarni. "One-pot synthesis of bicyclic sugar oxazolidinone from d-glucosamine". RSC Advances 5, n.º 29 (2015): 22426–30. http://dx.doi.org/10.1039/c5ra02270c.

Texto completo
Resumen
Herein we report a one-pot and efficient method for the synthesis of a 1,2-cis fused furanoside bicyclic oxazolidinone derivative of d-glucosamine via pyranose to furanose conversion and concomitant cyclization involving the N-Troc group.
Los estilos APA, Harvard, Vancouver, ISO, etc.
3

Asres, Daniel D. y Hélène Perreault. "Preparation, isolation, and characterization of permethylated galactosides and fucosides". Canadian Journal of Chemistry 77, n.º 3 (1 de marzo de 1999): 319–25. http://dx.doi.org/10.1139/v99-019.

Texto completo
Resumen
Sugar analysis involving permethylation followed by methanolysis can lead to significant results, given that permethylated monosaccharide standards are available for comparison of spectral and chromatographic data. Such standards are not readily commercially available, especially the furanoside forms. This note describes the isolation and characterization of permethylated pyranoside and furanoside species of D(+)-galactose and L(-)-fucose. Separation of the isomers was optimized using a combination of column chromatography and continuous elution thin-layer chromatography (TLC). TLC, gas chromatography - mass spectrometry, and 1H nuclear magnetic resonance (NMR) spectroscopy were used as the characterization methods. The isolation of furanosides is emphasized, since no specific NMR data have been reported on those to date, while several reports have already discussed the structural aspects of pyranosides.Key words: permethylation, monosaccharide, GC-MS, TLC, NMR.
Los estilos APA, Harvard, Vancouver, ISO, etc.
4

Asres, Daniel Derbie y Hélène Perreault. "Monosaccharide permethylation products for gas chromatography - mass spectrometry: how reaction conditions can influence isomeric ratios". Canadian Journal of Chemistry 75, n.º 10 (1 de octubre de 1997): 1385–92. http://dx.doi.org/10.1139/v97-166.

Texto completo
Resumen
Methylation analysis has been widely used for determination of carbohydrate structures by mass spectrometry. Permethylation of monosaccharides yields mixtures of anomeric pyranosides and furanosides. This paper discusses the influence of some of the permethylation reaction parameters on the proportions of isomeric products obtained. The ratios of three five- and six-membered ring products obtained from two permethylated monosaccharides, D-galactose and L-fucose, have been determined as a function of reaction parameters. The method of Ciucanu and Kerek (1) (methyl iodide in dimethyl sulfoxide (DMSO) in the presence of sodium hydroxide (NaOH)) was used as a starting point. The "conventional" method consists of mixing all of the reagents with the substrate and allowing the reaction to proceed with stirring. Both D-galactose and L-fucose under these conditions produced two main permethylated isomers, a furanoside and a pyranoside, along with two other minor isomeric components. We have investigated the effect on the proportion of products obtained of mixing DMSO, substrate, and NaOH for various times prior to the addition of methyl iodide. Results for D-galactose showed that shorter times enhanced the formation of permethylated furanoside isomers, while reducing the proportion of pyranosides. In other sets of experiments, the time and temperature of reaction, following the addition of methyl iodide, were studied. The indication is that 15 min are sufficient to produce complete methylation, with longer reaction times yielding the same results. Again for D-galactose, low reaction temperatures (ca. 10 °C) favored formation of furanoside products. Higher temperatures yielded higher pyranoside/furanoside ratios. Higher quantities of NaOH also favored formation of the main galactopyranoside product. As for L-fucose, the ratio of the main furanoside vs. pyranoside products obtained by permethylation varied in a way similar to permethylated galactoside. Thus, higher temperatures and longer reaction times favored the main fucopyranoside product. Gentler conditions (i.e., shorter reaction times and lower temperatures) significantly favored the formation of the main fucofuranoside product. These results are interesting as they show the possibility of controlling the relative abundance of permethylated isomers of fucose and galactose. They also constitute a warning to chemists who use methylation procedures in their analyses, to the effect that permethylation products may vary considerably if the reaction conditions are not carefully controlled. Keywords: glucose, galactose, fucose, TLC, GC–MS, permethylation, monosaccharides.
Los estilos APA, Harvard, Vancouver, ISO, etc.
5

Gerbst, Alexey G., Vadim B. Krylov y Nikolay E. Nifantiev. "Conformational changes in common monosaccharides caused by per-O-sulfation". Pure and Applied Chemistry 91, n.º 7 (26 de julio de 2019): 1223–29. http://dx.doi.org/10.1515/pac-2018-1212.

Texto completo
Resumen
Abstract Polysulfated carbohydrates play an important role in many biological processes because of their ability to bind to various protein receptors such as different growth factors, blood coagulation factors, adhesion lectins etc. Precise information about spatial organization of sulfated derivatives is of high demand for molecular modelling of such interactions as well as for understanding of the mechanism of pyranoside-into-furanoside rearrangement. In this review we summarize the changes recently revealed for the conformations of common pyranosides and furanosides upon total O-sulfation which were studied by means of NMR spectroscopy as well as molecular modelling. It was found that pentoses, being more flexible, undergo complete conformational chair inversion. Meanwhile, for hexoses the situation strongly depends on the monosaccharide configuration. Conformational changes are most pronounced in gluco-compounds though quantum chemical calculations helped to establish that no complete chair inversion occurred. In furanosides distortions of two types were observed: either the ring conformation or the conformation of the side chain changed. The presented data may be used for the analysis of chemical, physical and biological properties of sulfated carbohydrates.
Los estilos APA, Harvard, Vancouver, ISO, etc.
6

Argunov, D. A., V. B. Krylov y N. E. Nifantiev. "Convergent synthesis of isomeric heterosaccharides related to the fragments of galactomannan from Aspergillus fumigatus". Organic & Biomolecular Chemistry 13, n.º 11 (2015): 3255–67. http://dx.doi.org/10.1039/c4ob02634a.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
7

Egron, David, Thierry Durand, Arlene Roland, Jean-Pierre Vidal y Jean-Claude Rossi. "C-Furanoside Synthesis via Intramolecular Cyclization". Synlett 1999, n.º 4 (abril de 1999): 435–37. http://dx.doi.org/10.1055/s-1999-3157.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
8

Vinnitskiy, Dmitry Z., Vadim B. Krylov, Nadezhda E. Ustyuzhanina, Andrey S. Dmitrenok y Nikolay E. Nifantiev. "The synthesis of heterosaccharides related to the fucoidan from Chordaria flagelliformis bearing an α-l-fucofuranosyl unit". Organic & Biomolecular Chemistry 14, n.º 2 (2016): 598–611. http://dx.doi.org/10.1039/c5ob02040a.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
9

Hale, Karl J., Leslie Hough, Soraya Manaviazar y Andrew Calabrese. "Rules and Stereoelectronic Guidelines for the Anionic Nucleophilic Displacement of Furanoside and Furanose O-Sulfonates". Organic Letters 17, n.º 7 (17 de marzo de 2015): 1738–41. http://dx.doi.org/10.1021/acs.orglett.5b00511.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
10

Krylov, Vadim B., Lucia Paulovičová, Ema Paulovičová, Yury E. Tsvetkov y Nikolay E. Nifantiev. "Recent advances in the synthesis of fungal antigenic oligosaccharides". Pure and Applied Chemistry 89, n.º 7 (26 de julio de 2017): 885–98. http://dx.doi.org/10.1515/pac-2016-1011.

Texto completo
Resumen
AbstractThe driving force for the constant improvement and development of new synthetic methodologies in carbohydrate chemistry is a growing demand for biologically important oligosaccharide ligands and neoglycoconjugates thereof for numerous biochemical investigations such as cell-to-pathogen interactions, immune response, cell adhesion, etc. Here we report our syntheses of the spacer-armed antigenic oligosaccharides related to three groups of the polysaccharides of the fungal cell-wall including α- and β-mannan, α- and β-glucan and galactomannan chains, which include new rationally designed synthetic blocks, efficient solutions for the stereoselective construction of glycoside bonds, and novel strategy for preparation of furanoside-containing oligosaccharides based on recently discovered pyranoside-into-furanoside (PIF) rearrangement.
Los estilos APA, Harvard, Vancouver, ISO, etc.
11

Linden, A., C. K. Lee y X. Li. "A fused furanoside-1,4-lactone at 173K". Acta Crystallographica Section C Crystal Structure Communications 55, n.º 4 (15 de abril de 1999): 642–44. http://dx.doi.org/10.1107/s0108270198016692.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
12

Sharma, Gangavaram V. M., Gonuguntla Anjaiah, Marumudi Kanakaraju, Bommeda Sudhakar, Deepak Chatterjee y Ajit C. Kunwar. "Synthesis of a new β-amino acid with a 3-deoxy-l-ara furnaoside side chain: the influence of the side chain on the conformation of α/β-peptides". Organic & Biomolecular Chemistry 14, n.º 2 (2016): 503–15. http://dx.doi.org/10.1039/c5ob01753j.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
13

Lemaire, Sébastien, Amandine Xolin, Charlotte Gozlan y Vittorio Farina. "Stereoselective C-glycosylation of furanosyl halides with arylzinc reagents". Pure and Applied Chemistry 86, n.º 3 (20 de marzo de 2014): 329–33. http://dx.doi.org/10.1515/pac-2013-1029.

Texto completo
Resumen
Abstract Were are reporting a highly diastereoselective, transition-metal-free approach of C-aryl glycosides in the pyranoside and furanoside series by the direct coupling of glycosyl halides with diarylzinc reagents in a toluene/di-n-butyl ether solvent mixture.
Los estilos APA, Harvard, Vancouver, ISO, etc.
14

Taha, Hashem A., Michele R. Richards y Todd L. Lowary. "Conformational Analysis of Furanoside-Containing Mono- and Oligosaccharides". Chemical Reviews 113, n.º 3 (16 de octubre de 2012): 1851–76. http://dx.doi.org/10.1021/cr300249c.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
15

Velty, Rachel, Thierry Benvegnu, Muriel Gelin, Eric Privat y Daniel Plusquellec. "A convenient synthesis of disaccharides containing furanoside units". Carbohydrate Research 299, n.º 1-2 (marzo de 1997): 7–14. http://dx.doi.org/10.1016/s0008-6215(96)00268-6.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
16

Krylov, Vadim B., Dmitry A. Argunov y Nikolay E. Nifantiev. "Pyranoside-into-furanoside rearrangement of D-glucuronopyranoside derivatives". Mendeleev Communications 26, n.º 6 (noviembre de 2016): 483–84. http://dx.doi.org/10.1016/j.mencom.2016.11.007.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
17

Gerbst, Alexey G., Vadim B. Krylov, Dmitry A. Argunov, Andrey S. Dmitrenok y Nikolay E. Nifantiev. "Driving Force of the Pyranoside-into-Furanoside Rearrangement". ACS Omega 4, n.º 1 (14 de enero de 2019): 1139–43. http://dx.doi.org/10.1021/acsomega.8b03274.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
18

McAuliffe, Joseph C. y Ole Hindsgaul. "Use of Acyclic Glycosyl Donors for Furanoside Synthesis". Journal of Organic Chemistry 62, n.º 5 (marzo de 1997): 1234–39. http://dx.doi.org/10.1021/jo9618583.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
19

Krishnudu, Kasireddy, Palakodety Radha Krishna y Hari Babu Mereyala. "Pd(II)Cl2 mediated oxidative cycllsation of some 3-hydroxy 4-vinyl furanoside derivatives to synthetically valuable bis-furanosides". Tetrahedron Letters 37, n.º 33 (agosto de 1996): 6007–10. http://dx.doi.org/10.1016/0040-4039(96)01261-0.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
20

KRISHNUDU, K., P. R. KRISHNA y H. B. MEREYALA. "ChemInform Abstract: PdCl2-Mediated Oxidative Cyclization of Some 3-Hydroxy-4-vinyl- furanoside Derivatives to Synthetically Valuable Bis-Furanosides." ChemInform 27, n.º 48 (4 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199648226.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
21

Benning, Rajdeep K., Helen M. I. Osborn y Andrea Turkson. "Regioselective Beckmann rearrangements of furanoside and pyranoside-derived oximes". Tetrahedron: Asymmetry 22, n.º 1 (enero de 2011): 109–16. http://dx.doi.org/10.1016/j.tetasy.2010.11.031.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
22

Lee, Eun y Cheol Min Park. "C-furanoside synthesis via radical cyclisation of β-alkoxyacrylates". J. Chem. Soc., Chem. Commun., n.º 3 (1994): 293–94. http://dx.doi.org/10.1039/c39940000293.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
23

Guimet, Eugeni, Montserrat Diéguez, Aurora Ruiz y Carmen Claver. "Pd-catalyzed asymmetric allylic alkylation using furanoside diphosphinite ligands". Inorganica Chimica Acta 358, n.º 13 (septiembre de 2005): 3824–28. http://dx.doi.org/10.1016/j.ica.2005.06.004.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
24

Ray, Ankur y Sabiha Khan. "Convergent Synthesis of Novel Mono- and Di-substituted 1,2-Isopropylideneglucofuranose Appended Dendrimers with a Ferrocene Core and their Electrochemical Studies". Synlett 29, n.º 10 (10 de abril de 2018): 1367–72. http://dx.doi.org/10.1055/s-0037-1609490.

Texto completo
Resumen
Ferrocene-cored dendrimers incorporating 1,2-isopropylidenefuranose capped furanoside branches were synthesized and their electrochemical properties were studied. It was observed that the dendritic environment in the ferrocene dendrimers increased the E 1/2 values with increase in bulk of the dendrimer, as expected. The reversible nature of the redox process was maintained in all the dendrimers.
Los estilos APA, Harvard, Vancouver, ISO, etc.
25

Maier, Martin E. y Tilmann Brandstetter. "Synthesis of an oxabicyclo[7.2.1] enediyne from a furanoside derivative". Tetrahedron Letters 33, n.º 49 (1992): 7511–14. http://dx.doi.org/10.1016/s0040-4039(00)60810-9.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
26

Diéguez, Montserrat, Aurora Ruiz y Carmen Claver. "Chiral furanoside phosphite–phosphoroamidites: new ligands for asymmetric catalytic hydroformylation". Tetrahedron: Asymmetry 12, n.º 20 (noviembre de 2001): 2827–34. http://dx.doi.org/10.1016/s0957-4166(01)00489-x.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
27

Diéguez, Montserrat, Aurora Ruiz y Carmen Claver. "Tunable furanoside diphosphite ligands. A powerful approach in asymmetric catalysis". Dalton Trans., n.º 15 (2003): 2957–63. http://dx.doi.org/10.1039/b303303a.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
28

Taha, Hashem A., Michele R. Richards y Todd L. Lowary. "ChemInform Abstract: Conformational Analysis of Furanoside-Containing Mono- and Oligosaccharides". ChemInform 44, n.º 17 (4 de abril de 2013): no. http://dx.doi.org/10.1002/chin.201317278.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
29

MCAULIFFE, J. C. y O. HINDSGAUL. "ChemInform Abstract: Use of Acyclic Glycosyl Donors for Furanoside Synthesis." ChemInform 28, n.º 28 (3 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199728175.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
30

VELTY, R., T. BENVEGNU, M. GELIN, E. PRIVAT y D. PLUSQUELLEC. "ChemInform Abstract: A Convenient Synthesis of Disaccharides Containing Furanoside Units." ChemInform 28, n.º 27 (3 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199727230.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
31

Shi, Zhizhong, Lili Sun y Chunbao Li. "Solvent Polarity-Controlled Selective Synthesis of Methyl Pyranoside and Furanoside". Journal of Agricultural and Food Chemistry 62, n.º 14 (26 de marzo de 2014): 3287–92. http://dx.doi.org/10.1021/jf500144b.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
32

Pàmies, Oscar, Gino P. F. van Strijdonck, Montserrat Diéguez, Sirik Deerenberg, Gemma Net, Aurora Ruiz, Carmen Claver, Paul C. J. Kamer y Piet W. N. M. van Leeuwen. "Modular Furanoside Phosphite Ligands for Asymmetric Pd-Catalyzed Allylic Substitution". Journal of Organic Chemistry 66, n.º 26 (diciembre de 2001): 8867–71. http://dx.doi.org/10.1021/jo0159284.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
33

Hardacre, Christopher, Ivano Messina, Marie E. Migaud, Kerry A. Ness y Sarah E. Norman. "1,2-Cyclic sulfite and sulfate furanoside diesters: improved syntheses and stability". Tetrahedron 65, n.º 32 (agosto de 2009): 6341–47. http://dx.doi.org/10.1016/j.tet.2009.06.013.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
34

Guimet, Eugeni, Montserrat Diéguez, Aurora Ruiz y Carmen Claver. "Furanoside thioether–phosphinite ligands for Pd-catalyzed asymmetric allylic substitution reactions". Tetrahedron: Asymmetry 16, n.º 5 (marzo de 2005): 959–63. http://dx.doi.org/10.1016/j.tetasy.2004.11.094.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
35

Diéguez, Montserrat, Oscar Pàmies y Carmen Claver. "Furanoside thioether–phosphinite ligands for Rh-catalyzed asymmetric hydrosilylation of ketones". Tetrahedron: Asymmetry 16, n.º 23 (noviembre de 2005): 3877–80. http://dx.doi.org/10.1016/j.tetasy.2005.10.009.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
36

Nifantiev, Nikolay, Vadim Krylov, Dmitry Argunov, Dmitry Vinnitskiy, Alexey Gerbst, Nadezhda Ustyuzhanina y Andrey Dmitrenok. "The Pyranoside-into-Furanoside Rearrangement of Alkyl Glycosides: Scope and Limitations". Synlett 27, n.º 11 (6 de abril de 2016): 1659–64. http://dx.doi.org/10.1055/s-0035-1561595.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
37

LEE, E. y C. M. PARK. "ChemInform Abstract: C-Furanoside Synthesis via Radical Cyclisation of β- Alkoxyacrylates." ChemInform 25, n.º 23 (19 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199423227.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
38

Lak, Parnian, Spandana Makeneni, Robert J. Woods y Todd L. Lowary. "Specificity of Furanoside-Protein Recognition through Antibody Engineering and Molecular Modeling". Chemistry - A European Journal 21, n.º 3 (20 de noviembre de 2014): 1138–48. http://dx.doi.org/10.1002/chem.201405259.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
39

DENİZALTI, Serpil, Fatma ÇETİN TELLİ, Selin YILDIRAN, Azize Yeşim SALMAN y Bekir ÇETİNKAYA. "Newly synthesized furanoside-based NHC ligands for the arylation of aldehydes". TURKISH JOURNAL OF CHEMISTRY 40 (2016): 689–97. http://dx.doi.org/10.3906/kim-1603-95.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
40

Casali, Emanuele, Sirwan T. Othman, Ahmed A. Dezaye, Debora Chiodi, Alessio Porta y Giuseppe Zanoni. "Highly Stereoselective Glycosylation Reactions of Furanoside Derivatives via Rhenium (V) Catalysis". Journal of Organic Chemistry 86, n.º 11 (25 de mayo de 2021): 7672–86. http://dx.doi.org/10.1021/acs.joc.1c00706.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
41

Yan, Tu-Hsin, Hong-Jay Lo y Yuan-Kang Chang. "A C2-Symmetric Pool Based Synthesis of the Furanoside of Hygromycin A". HETEROCYCLES 86, n.º 1 (2012): 687. http://dx.doi.org/10.3987/com-12-s(n)19.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
42

Pàmies, Oscar, Gemma Net, Aurora Ruiz y Carmen Claver. "Asymmetric hydroformylation of styrene catalyzed by furanoside phosphine–phosphite–Rh(I) complexes". Tetrahedron: Asymmetry 12, n.º 24 (enero de 2002): 3441–45. http://dx.doi.org/10.1016/s0957-4166(02)00030-7.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
43

Ray, Ankur y Subir Ghorai. "Ferrocene cored dendrimers incorporating anthracene capped furanoside branches: synthesis and photophysical studies". Tetrahedron Letters 52, n.º 23 (junio de 2011): 2980–83. http://dx.doi.org/10.1016/j.tetlet.2011.03.137.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
44

MAIER, M. E. y T. BRANDSTETTER. "ChemInform Abstract: Synthesis of an Oxabicyclo(7.2.1) Enediyne from a Furanoside Derivative." ChemInform 24, n.º 17 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199317083.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
45

Pamies, Oscar, Gino P. F. van Strijdonck, Montserrat Dieguez, Sirik Deerenberg, Gemma Net, Aurora Ruiz, Carmen Claver, Paul C. J. Kamer y Piet W. N. M. van Leeuwen. "ChemInform Abstract: Modular Furanoside Phosphite Ligands for Asymmetric Pd-Catalyzed Allylic Substitution." ChemInform 33, n.º 26 (21 de mayo de 2010): no. http://dx.doi.org/10.1002/chin.200226110.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
46

Guimet, Eugeni, José Parada, Montserrat Diéguez, Aurora Ruiz y Carmen Claver. "Asymmetric hydroformylation of vinyl arenes catalyzed by furanoside diphosphinites-Rh(I) complexes". Applied Catalysis A: General 282, n.º 1-2 (marzo de 2005): 215–20. http://dx.doi.org/10.1016/j.apcata.2004.12.013.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
47

Wilson, Lawrence J., Michael W. Hager, Yahya A. El-Kattan y Dennis C. Liotta. "Nitrogen Glycosylation Reactions Involving Pyrimidine and Purine Nucleoside Bases with Furanoside Sugars". Synthesis 1995, n.º 12 (diciembre de 1995): 1465–79. http://dx.doi.org/10.1055/s-1995-4142.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
48

Majdecki, Maciej, Janusz Jurczak y Tomasz Bauer. "Palladium-Catalyzed Enantioselective Allylic Substitution in the Presence of Monodentate Furanoside Phosphoramidites". ChemCatChem 7, n.º 5 (21 de enero de 2015): 799–807. http://dx.doi.org/10.1002/cctc.201402933.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
49

Diéguez, Montserrat, Oscar Pàmies, Aurora Ruiz y Carmen Claver. "Synthesis and structural studies of rhodium(I)-catalytic precursors containing two furanoside diphosphines". Journal of Organometallic Chemistry 629, n.º 1-2 (junio de 2001): 77–82. http://dx.doi.org/10.1016/s0022-328x(01)00819-1.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
50

Islam, Shahidul M., Brandon Havranek, Zahin Ibnat y Pierre-Nicholas Roy. "New Insights into the Role of Hydrogen Bonding in Furanoside Binding to Protein". Journal of Physical Chemistry B 124, n.º 10 (19 de febrero de 2020): 1919–27. http://dx.doi.org/10.1021/acs.jpcb.9b11924.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
También puede estar interesado en las bibliografías sobre el tema "Furanoside" para otros tipos de fuentes:
Tesis
Ofrecemos descuentos en todos los planes premium para autores cuyas obras están incluidas en selecciones literarias temáticas. ¡Contáctenos para obtener un código promocional único!

Pasar a la bibliografía