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2 deoxy beta d ribose

2 deoxy beta d ribose

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2 deoxy beta d ribose
Deoxyribose - Wikipedia, 2-Deoxy-D-ribose | C5H10O4 - PubChem, 2-Deoxy-D-ribose 97% | Sigma-Aldrich, 2-Deoxy-D-ribose | Sigma-Aldrich, beta-D-2-Deoxyribose | C5H10O4 - PubChem, Conversion of 2-deoxy-D-ribose into 2-amino-5-(2-deoxy , 2-Deoxy-D-Ribose | C5H10O4 | ChemSpider, β-D-2-deoxyribose - Wikidata, Difference Between Deoxyribose and Ribose - pediaa.com.
2003 Sep 21;1(18):3160-72.Conversion of 2-deoxy-D-ribose into 2-amino-5-(2-deoxy-beta-D-ribofuranosyl)pyridine, 2'-deoxypseudouridine, and other C-(2'-deoxyribonucleosides).1, .Author information1Department of Chemistry, King's College London, Strand, London, UK WC2R 2LS. colin.reese@kcl.ac.ukAbstractThe synthesis of 2-amino-5-(2-deoxy-beta-D-ribofuranosyl)pyridine 2a, 2-amino-5-(2-deoxy-alpha-D-ribofuranosyl)-pyridine 23, 2-amino-5-(2-deoxy-beta-D-ribofuranosyl)-3-methylpyridine 2b, 2-amino-5-(2-deoxy-alpha-D-ribofuranosyl)-3-methylpyridine 29 and 5-(2-deoxy-beta-D-ribofuranosyl)-2,4-dioxopyrimidine [2'-deoxypseudouridine] 30a is described. These C-nucleosides are prepared either from 2-deoxy-3,5-O-(1,1,3,3-tetraisopropyldisiloxan-1,3-diyl)-D-ribofuranose 15 or from 2-deoxy-3,5-O-(1,1,3,3-tetraisopropyldisiloxan-1,3-diyl)-D-ribono-1,4-lactone 16, which are themselves prepared from 2-deoxy-D-ribose 13. The sugar derivatives are first allowed to react with the appropriate 5-lithio-pyridine or 5-lithio-pyrimidine derivatives, which are prepared from 5-bromo-2-(dibenzylamino)pyridine 12a, 5-bromo-2-[bis(4-methoxybenzyl)amino]pyridine 12b, 5-bromo-2-dibenzylamino-3-methylpyridine 25 and 5-bromo-2,4-bis(4-methoxybenzyloxy)pyrimidine 33. The products from the reactions between the lithio-derivatives and the lactol 15 are cyclized under Mitsunobu conditions; the products from the reactions between the lithio-derivatives and the lactone 16 are first reduced with L-Selectride before cyclization, also under Mitsunobu conditions. In all cases, the beta-anomers of the protected C-nucleosides are the predominant products. Finally, the separation of the alpha- and beta-anomers and the removal of all of the protecting groups are described.PMID: 14527147 [Indexed for MEDLINE] Publication type, MeSH terms, SubstancesPublication typeMeSH termsSubstancesLinkOut - more resourcesMiscellaneousNCI CPTAC Assay Portal. Deoxyribose, or more precisely 2-deoxyribose, is a monosaccharide with idealized formula H−(C=O)−(CH 2)−(CHOH) 3 −H. Its name indicates that it is a deoxy sugar, meaning that it is derived from the sugar ribose by loss of an oxygen atom.. 2-deoxy-D-ribose is a deoxypentose that is D-ribose in which the hydroxy group at position C-2 is replaced by hydrogen. It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite and a mouse metabolite. It derives from a.
MSMLS Online Plate Map. Metabolite descriptors included with the software download upon purchase of the product include: Name, Parent CID, molecular formula, molecular weight, CAS, ChEBI, HMDB ID, PubChem Compound and Subst. Use the product Attributes below to configure the comparison table. (Select up to %1% total). beta-D-2-Deoxyribose | C5H10O4 | CID 439576 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities . 1. Org Biomol Chem. 2003 Sep 21;1(18):3160-72. Conversion of 2-deoxy-D-ribose into 2-amino-5-(2-deoxy-beta-D-ribofuranosyl)pyridine, 2'-deoxypseudouridine, and other C-(2'-deoxyribonucleosides).. A deoxypentose that is D-ribose in which the hydroxy group at position C-2 is replaced by hydrogen. ChEBI CHEBI:28816. This page was last edited on 13 April 2019, at 09:57. All structured data from the main, property and lexeme namespaces is available under the Creative Commons CC0 License; text in the other namespaces is available under the Creative Commons Attribution-ShareAlike License; additional terms may apply..
 
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