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5-O-tert-butyldiphenylsilyl-α,β-L-arabinofuranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103763-13-9

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103763-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103763-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,6 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 103763-13:
(8*1)+(7*0)+(6*3)+(5*7)+(4*6)+(3*3)+(2*1)+(1*3)=99
99 % 10 = 9
So 103763-13-9 is a valid CAS Registry Number.

103763-13-9Relevant academic research and scientific papers

Total Synthesis, Configuration Assignment, and Cytotoxic Activity Evaluation of Protulactone A

Markovi?, Martin,Koó?, Peter,?arny, Tomá?,Sokoliová, Saskia,Bohá?iková, Nikola,Moncol′, Ján,Gracza, Tibor

, p. 1631 - 1638 (2017)

The first total synthesis and absolute configuration assignment of protulactone A (1) has been achieved. Four stereoisomers, 1a, ent-1a, 1b, and ent-1b, of this natural polyketide were prepared by chiral pool synthesis starting from l- and d-arabinose, re

Amipurimycin: Total Synthesis of the Proposed Structures and Diastereoisomers

Wang, Shengyang,Sun, Jiansong,Zhang, Qingju,Cao, Xin,Zhao, Yachen,Tang, Gongli,Yu, Biao

supporting information, p. 2884 - 2888 (2018/02/16)

The proposed diastereoisomers (1 a–d) together with their C8′-epimers (1 e–h) of amipurimycin, a unique antifungal peptidyl nucleoside antibiotic, have been synthesized for the first time. The synthetic approach is efficient and stereodivergent, and features a stereoselective aldol condensation to build the branched C9 sugar amino acid skeleton and a regio- and stereocontrolled gold(I)-catalyzed N-glycosylation to furnish the purine nucleoside. Analysis of the NMR data suggests that the previously assigned configuration of the tertiary C3′ in amipurimycin should be of opposite configuration.

L-nucleoside compounds and application thereof

-

Paragraph 0162; 0164; 0165; 0166, (2016/11/02)

The invention discloses L-nucleoside compounds having the structure characteristic represented by the formula (I) or pharmaceutically acceptable salts thereof, and belongs to the technical field of pharmaceutical chemistry. The compounds can inhibit the activity of RNA viral polymerase, so the compounds can be used as potential drugs for prevention and treatment of infection of RNA viruses such as HCV, influenza virus, HRV (rhinovirus), RSV, Ebola virus, dengue virus, intestinal virus and the like.

Deoxygenation at the C3 position of d- and l-arabinofuranose: Stereospecific access to enantiomeric cordycepose derivatives

Da Paix?o Soares, Fábio,Silva, Maria Joselice E,Doboszewski, Bogdan

, p. 143 - 148 (2013/10/01)

Efficient synthesis of 3-deoxy-1,2-O-isopropylidene-β-d- and β-l-threo-pentofuranose (1,2-O-isopropylidene-β-d- and β-l-cordycepose) was accomplished starting from d- and l-arabinofuranose derivatives, respectively, by the action of LiBH(Et)3 on corresponding intermediate 3-O-lyxofuranosyl trifluoromethanesulfonates.

Synthesis of cis - And trans-α-l-[4.3.0]bicyclo-DNA monomers for antisense technology: Methods for the diastereoselective formation of bicyclic nucleosides

Hanessian, Stephen,Schroeder, Benjamin R.,Merner, Bradley L.,Chen, Bin,Swayze, Eric E.,Seth, Punit P.

, p. 9051 - 9063 (2013/10/08)

Two α-l-ribo-configured bicyclic nucleic acid modifications, represented by analogues 12 and 13, which are epimeric at C3′ and C5′ have been synthesized using a carbohydrate-based approach to build the bicyclic core structure. An intramolecular l-proline-mediated aldol reaction was employed to generate the cis-configured ring junction of analogue 12 and represents a rare application of this venerable organocatalytic reaction to a carbohydrate system. In the case of analogue 13, where a trans-ring junction was desired, an intermolecular diastereoselective Grignard reaction followed by ring-closing metathesis was used. In order to set the desired stereochemistry at the C5′ positions of both nucleoside targets, a study of diastereoselective Lewis acid mediated allylation reactions on a common bicyclic aldehyde precursor was carried out. Analogue 12 was incorporated in oligonucleotide sequences, and thermal denaturation experiments indicate that it is destabilizing when paired with complementary DNA and RNA. However, this construct shows a significant improvement in nuclease stability relative to a DNA oligonucleotide.

BICYCLIC NUCLEOSIDES AND OLIGOMERIC COMPOUNDS PREPARED THEREFROM

-

Page/Page column 113, (2012/01/05)

The present invention provides novel 3', 5 '-linked bicyclic nucleosides and oligomeric compounds prepared therefrom. The bicyclic nucleosides provided herein are useful for enhancing one or more properties of the oligomeric compounds they are incorporated into such as nuclease resistance.

Simple approach to 1-O-protected (R)- and (S)-glycerols from l- and d-arabinose for glycerol nucleic acids (GNA) monomers research

Doboszewski, Bogdan,Herdewijn, Piet

scheme or table, p. 3853 - 3855 (2011/08/06)

5-O-Protected (-Tr, -Sitert-BuPh2) d- and l-arabinofuranoses easily available in multigram quantities were converted to (S)- and (R)-1-O-protected glycerols, respectively, via oxidation (NaIO4) and reduction (NaBH4). Sourc

Intermediate compounds for preparing macrocylcic analogs

-

Page column 10,28, (2008/06/13)

Intermediate compounds of the formulas for use in the preparation of macrocyclic analogs.

An enantiospecific synthesis of the human cytomegalovirus antiviral agent [(R)-3-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)-4- hydroxybutyl]phosphonic acid

Chamberlain,Biron,Dornsife,Averett,Beauchamp,Koszalka

, p. 1371 - 1377 (2007/10/02)

The racemic isosteric phosphonate of ganciclovir monophosphate (BW2482U89, SR3745, [3-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)-4- hydroxybutyl]phosphonic acid, 1) has potent and selective in vitro activity against human cytomegalovirus. An enant

Rapid synthesis of 5-O-(tert-butyldiphenylsilyl)-2-deoxy-L-ribonolactone

Sharma,Marquez

, p. 1937 - 1945 (2007/10/02)

A convenient, four-step synthesis of the title compound (1) in 21% overall yield from L-arabinose is described. Selective formation of the 2-O-phenoxythiocarbonyl derivative 6 and its tributyltin hydride/azobis(isobutyronitrile) deoxygenation performed in

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