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tert-butyl(((2R,3S)-3-((tert-butyldiphenylsilyl)oxy)-5-methoxytetrahydrofuran-2-yl)methoxy)diphenylsilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

148903-86-0

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148903-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148903-86-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,9,0 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 148903-86:
(8*1)+(7*4)+(6*8)+(5*9)+(4*0)+(3*3)+(2*8)+(1*6)=160
160 % 10 = 0
So 148903-86-0 is a valid CAS Registry Number.

148903-86-0Downstream Products

148903-86-0Relevant academic research and scientific papers

Highly Stereoselective Glycosylation Reactions of Furanoside Derivatives via Rhenium (V) Catalysis

Casali, Emanuele,Othman, Sirwan T.,Dezaye, Ahmed A.,Chiodi, Debora,Porta, Alessio,Zanoni, Giuseppe

, p. 7672 - 7686 (2021/06/21)

A novel approach for the formation of anomeric carbon-functionalized furanoside systems was accomplished through the employment of an oxo-rhenium catalyst. The transformation boasts a broad range of nucleophiles including allylsilanes, enol ethers, and aromatics in addition to sulfur, nitrogen, and hydride donors, able to react with an oxocarbenium ion intermediate derived from furanosidic structures. The excellent stereoselectivities observed followed the Woerpel model, ultimately providing 1,3-cis-1,4-trans systems. In the case of electron-rich aromatic nucleophiles, an equilibration occurs at the anomeric center with the selective formation of 1,3-trans-1,4-cis systems. This anomalous result was rationalized through density functional theory calculations. Different oxocarbenium ions such as those derived from dihydroisobenzofuran, pyrrolidine, and oxazolidine heterocycles can also be used as a substrate for the oxo-Re-mediated allylation reaction.

Synthesis of disaccharide nucleosides by the O-glycosylation of natural nucleosides with thioglycoside donors

Aoki, Shin,Fukumoto, Taketo,Itoh, Taiki,Kurihara, Masayuki,Saito, Shigeto,Komabiki, Shin-Ya

, p. 740 - 751 (2015/06/02)

Disaccharide nucleosides constitute an important group of naturally-occurring sugar derivatives. In this study, we report on the synthesis of disaccharide nucleosides by the direct O-glycosylation of nucleoside acceptors, such as adenosine, guanosine, thy

Synthesis and Characterization of Oligonucleotides Containing the C4′-Oxidized Abasic Site Produced by Bleomycin and Other DNA Damaging Agents

Kim, Jaeseung,Gil, Jun Mo,Greenberg, Marc M.

, p. 5882 - 5885 (2007/10/03)

Selective introduction of damage: The C4′-position of DNA serves as the site of attack for a number of DNA damaging agents, including bleomycin. The C4′-abasic site is a major product found in damaged DNA following abstraction of the hydrogen atom from th

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