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tert-Butyldimethylsilyl-2-azido-3,6-di-O-benzyl-2-desoxy-β-D-glucopyranosid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120312-09-6

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120312-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120312-09-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,3,1 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120312-09:
(8*1)+(7*2)+(6*0)+(5*3)+(4*1)+(3*2)+(2*0)+(1*9)=56
56 % 10 = 6
So 120312-09-6 is a valid CAS Registry Number.

120312-09-6Relevant articles and documents

One-Pot Protection Strategy of Glucosamine to Assemble Building Blocks of Chitosan and Lipid A

Chen, Jyun-Siao,Huang, Po-Hsun,Lin, Yi-Jyun,Liu, Jen-Wei,Liu, Yu-Hao,Luo, Shun-Yuan,Pantawane, Amit Ravindra,Sankar, Arumugam,Wu, Hsin-Ru

, (2020/08/21)

This investigation describes a one-pot reaction to prepare a series of building blocks for glycosylation reactions, such as 3-alcohol glucosamines, fully protected glucosamines, O-4 and O-6 alcohol glucosamines. These reactions readily produce not only gl

Toward the solid-phase synthesis of heparan sulfate oligosaccharides: Evaluation of iduronic acid and idose building blocks

Guedes, Nerea,Czechura, Pawel,Echeverria, Begona,Ruiz, Ada,Michelena, Olatz,Martin-Lomas, Manuel,Reichardt, Niels-Christian

, p. 6911 - 6934 (2013/08/23)

Glycan arrays have been established as the premier technical platform for assessing the specificity of carbohydrate binding proteins, an important step in functional glycomics research. Access to large libraries of well-characterized oligosaccharides rema

A Suzuki-Miyaura coupling mediated deprotection as key to the synthesis of a fully lipidated malarial GPI disaccharide

Liu, Xinyu,Seeberger, Peter H.

, p. 1708 - 1709 (2007/10/03)

Ligandless palladium-catalyzed Suzuki-Miyaura coupling converted an inert p-bromobenzyl ether to a DDQ-labile p-(3,4-dimethoxyphenyl) benzyl ether in the presence of azide functionality and this strategy serves as a key step for the convergent synthesis of a fully lipidated malaria GPI disaccharide.

Modular synthesis of heparin oligosaccharides

Orgueira, Hernan A.,Bartolozzi, Alessandra,Schell, Peter,Litjens, Remy E. J. N.,Palmacci, Emma R.,Seeberger, Peter H.

, p. 140 - 169 (2007/10/03)

A general, modular strategy for the first completely stereoselective synthesis of defined heparin oligosaccharides is described. Six monosaccharide building blocks (four differentially protected glucosamines, one glucuronic and one iduronic acid) were uti

Solid- and solution-phase synthesis of heparin and other glycosaminoglycans

-

, (2008/06/13)

Described is a modular, general synthetic strategy for the preparation in solution and on a solid support of heparin, heparin-like glycosaminoglycans, glycosaminoglycans and non-natural analogs of each of them. Additionally, the modular strategy provides

Stereoselective synthesis of glycobiosyl phosphatidylinositol, a part structure of the glycosylphosphatidylinositol (GPI) anchor of Trypanosoma brucei

Murakata, Chikara,Ogawa, Tomoya

, p. 75 - 92 (2007/10/02)

O-α-D-Mannopyranosyl-(1 -> 4)-O-2-amino-2-deoxy-α-D-glucopyranosyl-(1 -> 6)-1D-myo-inositol 1-(1,2-di-O-myristoyl-sn-glycer-3-yl hydrogen phosphate), a part structure of the glycosyl-phosphatidylinositol (GPI) anchor of Trypanosoma brucei, was synthesised

Electrochemical Oxidation of Proline Derivatives: Total Syntheses of Bulgecinine and Bulgecin C

Barrett, Anthony G. M.,Pilipauskas, Daniel

, p. 2787 - 2800 (2007/10/02)

The influence of structure on the efficiency of the electrochemical C-5 oxidation of (2S,4S)-hydroxyproline carbamate esters is presented.Optimum methoxylation was observed with (2S,4S)-4-acetoxy-1,2-pyrrolidine-dicarboxylic acid 2-methyl 1-(2-(trimethylsilyl)ethyl) ester (19).The corresponding C-5 methoxy derivative 20 was converted into bulgecinine (4) via a stereospecific radical homologation to incorporate the C-5 hydroxymethyl substituent.Bulgecin C (1c) was prepared via a β-stereoselective glycosidation reaction using a 2-azido-2-deoxy-α-D-glucopyranosyl trichloroacetimidate derivative, regiospecific C-4' sulfation, and deprotection.

SYNTHETIC STUDY ON GLYCOPHOSPHATIDYL INOSITOL (GPI) ANCHOR OF TRYPANOSOMA BRUCEI: GLYCOHEPTAOSYL CORE

Murakata, Chikara,Ogawa, Tomoya

, p. 2439 - 2442 (2007/10/02)

A stereocontrolled approach to the synthesis of glycoheptaosyl core of glycophosphatidyl inositol (GPI) anchor of Trypanosoma brucei is described for the first time.

Glycosyl Imidates, 41. - 6-O-Benzyl-Protected Muramic Acid as Glycosyl Acceptor. - Synthesis of the GlcNAc-β-(1->4)MurNAc Disaccharide

Termin, Andreas,Schmidt, Richard R.

, p. 789 - 796 (2007/10/02)

The α-trichloroacetimidates 1 and 2 as glucosamine donors afford with the 6-O-benzyl-protected muramic acid 6a as acceptor the β-connected disaccharides 14 and 15, respectively, in high yields.Compound 14 furnishes by cleavage of the TBDMS group, transfor

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