20880-54-0

Upstream product

• 19186-38-0 O¹,O³,O⁴-Triacetyl-α-D-xylopyranose 
• 74-88-4 methyl iodide 
• 67-56-1 methanol 
• 4049-33-6 tetra-O-acetyl-β-D-xylopyranose 
• 90899-20-0 4-[β-D-xylopyranosyl-(1→6)-β-D-glucopyranosyl]-styrene 
• 108-24-7 acetic anhydride 
• 66648-51-9 miyaginin 
• 91-09-8 methyl α-L-xylopyranoside 
• 95851-48-2 C₄₂H₆₈O₁₂ 
• 91-09-8 methyl α,β-L-xyloside 
• 612-05-5 methyl-β-D-xylopyranoside 
• 53448-52-5 methyl β-L-xylopyranoside 

Downstream Products

• 74162-08-6 methyl 2,4-di-O-acetyl-β-D-xylopyranoside 
• 41897-35-2 methyl 2-mono-O-acetyl-β-D-xylopyranoside 
• 91-09-8 methyl-α-D-xylopyranoside 
• 612-05-5 methyl-β-D-xylopyranoside 
• 77217-82-4 methyl 3,4-di-O-acetyl-β-D-xylopyranoside 

Relevant academic research and scientific papers

ACTIVE AGENTS AND METHODS OF THEIR USE FOR THE TREATMENT OF METABOLIC DISORDERS AND NONALCOHOLIC FATTY LIVER DISEASE

Disclosed herein are active agents, compositions containing them, unit dosage forms containing them, and methods of their use, e.g., for treating a metabolic disorder or nonalcoholic fatty liver disease or for modulating a metabolic marker or nonalcoholic fatty liver disease marker.

Synthesis of C7-C16-alkyl glycosides: Part II - Synthesis of alkyl d-xylopyranosides in the presence of tin(IV) chloride as a Lewis acid catalyst

The Lewis acid catalyzed glycosylation reaction of β-peracetylated sugar derivatives (xylose) with fatty alkanols is used in a synthesis of C7-C16-alkyl D-xylopyranosides. The process occurs under the influence of tin(IV) chloride.

Synthesis of acylated methyl β-D-xylopyranosides and their enzymic deacylations by rabbit serum esterases

Selective pivaloylations of methyl β-D-xylopyranoside have been studied under various reaction conditions. Partially pivaloylated products were submitted to additional acetylations. The structures were established by 1H NMR spectroscopy. Representatives of acylated methyl β-D-xylopyranosides (acyl being pivaloyl, acetyl, or a combination of both) were submitted to hydrolysis catalyzed by rabbit serum and esterases isolated from rabbit serum.

Oviposition Deterrent of a Rutaceae-feeding Swallowtail Butterfly, Papilio xuthus, from a Non-host Rutaceous Plant, Orixa japonica

Females of the Rutaceae-feeding swallowtail butterfly, Papilio xuthus, do not oviposit on the rutaceous plant, Orixa japonica.A methanolic extract of O. japonica leaves was found to contain contact-chemical factors which deterred oviposition of the butter

Structure and Synthesis of Miyaginin, a p-Allylphenyl Glycoside from Lespedeza thunbergii forma macrantha

The structure of miyaginin previously reported as p-vinylphenyl O-D-xylosyl-(1->6)-D-glucoside without stereochemical assignment of two glycosidic linkages was reinvestigated by spectral and chemical means and shown to be revised as p-allylphenyl O-β-D-xylopyranosyl-(1->6)-β-D-glucopyranoside (p-allylphenyl β-primeveroside).In order to confirm the revised structure, an unambiguous synthesis of miyaginin was performed.

ISOLATION AND STRUCTURES OF TWO NEW p-HYDROXYSTYRENE GLYCOSIDES, PTELATOSIDE-A AND PTELATOSIDE-B FROM BRACKEN, PTERIDIUM AQUILINUM VAR. LATIUSCULUM, AND SYNTHESIS OF PTELATOSIDE-A

Two new p-hydroxystyrene glycosides, ptelatoside-A and ptelatoside-B were isolated from the carcinogenic fraction of aqueous extracts of bracken, Pteridium aquilinum var. latiusculum, and their structures were established to be p-β-primeverosyloxystyrene and p-β-neohesperidosyloxystyrene, respectively by chemical and spectral means.A synthesis of ptelatoside-A was achieved.