Category: 130539-43-4

On June 13, 2008, Minuth, Tobias; Boysen, Mike M. K. published an article.Product Details of 130539-43-4 The title of the article was A general and efficient route to 3-O-modified carbohydrate bis(oxazoline) ligands. And the article contained the following:

An efficient route to derivatives of carbohydrate-based bis(oxazoline) ligands with 3-O substituents of varying steric demand is described. The synthesis of the new ligands proceeds via a thioglucoside key intermediate. The double cyclization to the desired bis(oxazolines) is initiated with N-iodosuccinimide under mild conditions. Employing this strategy, four new 3-O-modified bis(oxazoline) ligands were obtained in good yields. The experimental process involved the reaction of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside(cas: 130539-43-4).Product Details of 130539-43-4

The Article related to thioglucoside malonamide cyclization, glucosamine oxazoline chiral ligand asym synthesis, Carbohydrates: Amines and other aspects.Product Details of 130539-43-4

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Li, Wei; Gao, Yu; Li, Qing; Li, Zhong-Jun published an article in 2018, the title of the article was Ionic-liquid supported rapid synthesis of an N-glycan core pentasaccharide on a 10 g scale.Quality Control of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside And the article contains the following content:

A new and efficient Ionic Liquid-Supported Oligosaccharide Synthesis (ILSOS) strategy for an N-linked core pentasaccharide on a 10 g scale is reported. This new ILSOS includes a new spacer for an IL support, a new tagging strategy, and fast, efficient and orthogonal removal of the ionic-liquid support, producing the N-linked core pentasaccharide with direct applicability potential in a short time, with high yield and on a large gram scale. The experimental process involved the reaction of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside(cas: 130539-43-4).Quality Control of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside

The Article related to glycan pentasaccharide ionic liquid supported synthesis orthogonal protecting group, Carbohydrates: Amines and other aspects.Quality Control of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

On August 31, 2005, Sundgren, Andreas; Lahmann, Martina; Oscarson, Stefan published an article.Formula: C16H19NO6S The title of the article was Block synthesis of Streptococcus pneumoniae type 14 capsular polysaccharide structures. And the article contained the following:

Synthesis of a thioglycoside tetrasaccharide block, β-D-Galp-(1â†?)-β-DGlcp-(1â†?)-[β-D-Galp-(1â†?)]-β-D-GlcNPhthp-(1→SEt), corresponding to the repeating unit of Streptococcus pneumoniae serotype 14 CPS is described. Coupling of this block with a spacer followed by removal of an isopropylidene acetal yielded an acceptor, which was elongated with the donor block to give a protected dimer of the repeating unit. Iteration of this methodol. yielded the trimer. Deprotection then produced an octa and a dodecasaccharide derivative ready for conjugation to proteins to afford immunoactive glycoconjugates. The experimental process involved the reaction of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside(cas: 130539-43-4).Formula: C16H19NO6S

The Article related to capsular polysaccharide preparation streptococcus pneumoniae, Carbohydrates: Amines and other aspects.Formula: C16H19NO6S

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Peters, J. L.; Wesselius, J. C.; Georghiou, K. C.; Kendrick, R. E.; Van Tuinen, A.; Koornneef, M. published an article in 1991, the title of the article was The physiology of photomorphogenetic tomato mutants.Product Details of 130539-43-4 And the article contains the following content:

A review with 37 references Photomorphogenesis of higher plants is a complex process resulting from the co-action of at least 3 different photoreceptors: phytochrome, a blue light (B)/UV-A photoreceptor (cryptochrome) and a UV-B photoreceptor. The existence of multiple photoreceptor types, e.g. type I (PI) or light-labile phytochrome and type II (PII) or light-stable phytochrome, adds to the complexity. The assignment of specific functions to the distinct mol. species of the photoreceptor is therefore being studied with the aid of photomorphogenetic mutants in which certain parts of the morphogenetic pathway are eliminated or altered. The relevance of the changed part in the mutant is directly indicated by its difference in response compared to its isogenic wild type. Mutants can be found (isolated) from natural populations or varieties (cultivars) or more efficiently after mutagenic treatment: using e.g. chems., irradiation; somaclonal variation; transposon insertion; transformation; introduction of antisense RNA. Photomorphogenetic mutants can be divided into three groups: photoreceptor mutants, lacking the photoreceptor or containing a modified photoreceptor which is non-functional; transduction chain mutants and response mutants. The first two will be pleiotropic for all responses regulated by the photoreceptor, while the latter are modified with respect to particular responses. Tomato (Lycospersicon esculentum) has several features which make it suitable for genetic anal. It is widely studied since it is a crop species of economic importance and many mutants are available. In addition it has a relatively small genome, is diploid with 12 chromosomes, is self pollinating, individual plants producing a large number (≈2000) of relatively large seeds which result in seedlings suitable for physiol. anal. and it is amenable for Agrobacterium-mediated transformation. Mutants of tomato which are important for the study of photomorphogenesis are discussed. The experimental process involved the reaction of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside(cas: 130539-43-4).Product Details of 130539-43-4

The Article related to review tomato photomorphogenesis mutant, Plant Biochemistry: Reviews and other aspects.Product Details of 130539-43-4

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

On January 11, 1996, Reddy, Gurijala V.; Jain, Rakesh K.; Locke, Robert D.; Matta, Khushi L. published an article.Related Products of 130539-43-4 The title of the article was Synthesis of precursors for the dimeric 3-O-SO3Na LewisX and LewisA structures. And the article contained the following:

Stereoselective syntheses of 3-O-SO3Na-β-Gal-(1→4)-β-GlcNAc-(1→3)-β-Gal-(1→4)-GlcNAc-β-OBn (I) and 3-O-SO3Na-β-Gal-(1→3)-β-GlcNAc-(1→3)-β-Gal-(1→3)-β-GlcNAc-(1→3)-β-Gal-(1→4)-Glc-β-OBn (II) were accomplished through the use of two novel glycosyl donors, namely, Et O-(2,6-di-O-acetyl-3,4-O-isopropylidene-β-D-galactopyranosyl)-(1→4)-3-O-acetyl-2-deoxy-2-phthalimido-1-thio-6-O-trimethylacetyl-β-D-glucopyranoside (III) and Et O-(2,6-di-O-acetyl-3,4-O-isopropylidene-β-D-galactopyranosyl)-(1→3)-4-O-acetyl-2-deoxy-2-phthalimido-1-thio-6-O-trimethylacetyl-β-D-glucopyranoside (IV). The experimental process involved the reaction of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside(cas: 130539-43-4).Related Products of 130539-43-4

The Article related to lewis oligosaccharide precursor stereoselective synthesis, Carbohydrates: Oligosaccharides and other aspects.Related Products of 130539-43-4

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

On July 24, 1992, Spijker, Nynke M.; Westerduin, Pieter; Van Boeckel, Constant A. A. published an article.Related Products of 130539-43-4 The title of the article was Synthesis of a pentasaccharide and a heptasaccharide corresponding to an ovarian glycoprotein; studies towards glycosylations. And the article contained the following:

Oligosaccharides I (R = H, R1), which correspond to an ovarian O-glycoprotein, were prepared via glycosidation reactions. The experimental process involved the reaction of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside(cas: 130539-43-4).Related Products of 130539-43-4

The Article related to oligosaccharide preparation fragment ovarian glycoprotein, Carbohydrates: Oligosaccharides and other aspects.Related Products of 130539-43-4

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Sau, Abhijit; Misra, Anup Kumar published an article in 2011, the title of the article was Environmentally Benign Preparation of Benzylidene Acetal of Carbohydrate Derivatives in PEG 600.Formula: C16H19NO6S And the article contains the following content:

An environmentally benign preparation of benzylidene acetal of carbohydrate derivatives catalyzed by HClO4-SiO2 in PEG 600 as solvent has been developed. Yields were excellent in every case. The experimental process involved the reaction of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside(cas: 130539-43-4).Formula: C16H19NO6S

The Article related to benzylidene acetal glycoside preparation, Carbohydrates: Monosaccharides, Glycals and other aspects.Formula: C16H19NO6S

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

On May 17, 2011, Seeberger, Peter H.; Hewitt, Michael C.; Snyder, Daniel A. published a patent.Quality Control of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside The title of the patent was Solid-phase and solution-phase synthesis of glycosylphosphatidylinositol glycans. And the patent contained the following:

One aspect of the present invention relates to solution-phase approaches to GPI synthesis. Another aspect of the present invention relates to key building blocks, and syntheses thereof, useful for GPI assembly. Yet another aspect of the invention relates to an automated method for the synthesis of GPIs and fragments thereof. The experimental process involved the reaction of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside(cas: 130539-43-4).Quality Control of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside

The Article related to glycosylphosphatidylinositol oligosaccharide glycan solid phase synthesis vaccine human, Carbohydrates: Alditols, Cyclitols, Glycerides and other aspects.Quality Control of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

On May 20, 2021, Wyand, Michael; Patel, Suman; Swiss, Gerald F. published a patent.Related Products of 130539-43-4 The title of the patent was Low contaminant vaccines against microbes possessing a cell wall structure comprising poly-β-(1→6)-glucosamine (PNAG). And the patent contained the following:

Disclosed are antimicrobial vaccines comprising oligosaccharide β-(1→6)-glucosamine groups linked units onto a tetanus toxoid carrier, wherein less than about 40% of the total number of such units are N-acetylated. The experimental process involved the reaction of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside(cas: 130539-43-4).Related Products of 130539-43-4

The Article related to antimicrobial vaccine cell wall beta glucosamine oligosaccharide, vaccine oligosaccharide beta glucsosamine tetanus toxoid carrier, Pharmaceuticals: Formulation and Compounding and other aspects.Related Products of 130539-43-4

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

On March 4, 2021, Dabora, Rebecca; Dingley, Amy; Patel, Suman; Swiss, Gerald F. published a patent.HPLC of Formula: 130539-43-4 The title of the patent was Tetanus toxoid and other antimicrobial vaccine compositions providing natural immunity against microbes with N-acetyl-β-(1->6)-glucosamine in cell wall. And the patent contained the following:

This invention is directed to antimicrobial vaccine compounds and compositions comprising oligosaccharide β-(1→6)- glucosamine groups having from 3 to 12 glucosamine units linked through a linker group to tetanus toxoid wherein the toxoid is primarily in its monomeric form. This invention is also directed to vaccine compositions that provide natural immunity against microbes possessing a cell wall structure that comprises oligosaccharide N-acetyl-β-(1→6)-glucosamine (PNAG) structures. The experimental process involved the reaction of Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside(cas: 130539-43-4).HPLC of Formula: 130539-43-4

The Article related to antimicrobial vaccine cell wall beta glucosamine antigen oligosaccharide, tetanus toxoid vaccine oligosaccharide beta glucsosamine, Immunochemistry: Adjuvants, Antigens, Haptens, and Vaccines and other aspects.HPLC of Formula: 130539-43-4

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles