Polyvinyl trisulfonate ethylamine based solid acid catalyst for the efficient glycosylation of sugars under solvent free conditions
作者:Avinash A. Chaugule、Amol R. Jadhav、Hern Kim
DOI:10.1039/c5ra20300g
日期:——
We have synthesized Brønsted solid acid catalysts which exhibited effective catalytic activity for acid catalyzed glycosylation reactions.
我们合成了Brønsted固体酸催化剂,对酸催化的糖基化反应表现出有效的催化活性。
Ionic liquid promoted atom economic glycosylation under Lewis acid catalysis
作者:Jacques Augé、Gwenaëlle Sizun
DOI:10.1039/b904692e
日期:——
Straightforward glycosylation of various alcohols with unprotected and non-activated monosaccharides were performed under scandium triflate catalysis. Rate and yield of glycosylation were highly improved when using 1-butyl-3-methylimidazolium trifluoromethanesulfonate as a green solvent. This ionic liquid was allowed to be recycled at least three times without loss of activity. The possibility of drastically reducing the amounts of catalyst (down to 1 mol%) and aglycone (down to 1 equiv) when performing the reaction in ionic liquid opens new perspectives in O-glycosylation, as a direct coupling between an aglycone and free sugars.
Surfactants of biological origin: The role of Mo(VI) and microwaves in the synthesis of xylan-based non-ionic surfactants
作者:Zuzana Hricovíniová
DOI:10.1016/j.carbpol.2016.02.070
日期:2016.6
glycosylation of unprotected d-xylose and d-lyxose, obtained after tandem Mo(VI)-catalyzed xylan hydrolysis-epimerization reaction, provides alkyl xylosides and lyxosides in short reaction times. A homologous series of amphiphilic alkyl pentosides varying in chain structure (C8-C14) was prepared in very good yields (38-73%). A new catalytic approach using the reusable heterogeneous PMoA/SiO2 catalyst provides
Boronic Acids as Phase-Transfer Reagents for Fischer Glycosidations in Low-Polarity Solvents
作者:Sanjay Manhas、Mark S. Taylor
DOI:10.1021/acs.joc.7b01880
日期:2017.11.3
Protocols employing phenylboronic acid as a phase-transfer reagent for Fischer glycosidations in low-polarity organic solvents are described. In addition to providing rate acceleration, the formation of a substrate-derived boronic ester alters the course of the reaction by selective promotion of a furanoside- or pyranoside-selective pathway. Computational modeling of the relative energies of the glycoside-derived
D-Xylopyranoside series compounds and therapeutical compositions containing same
申请人:Seikagaku Kogyo Co. Ltd.
公开号:EP0118676A1
公开(公告)日:1984-09-19
Disclosed are D-xylopyranoside series compounds represented by the following general formula:
in which R1 represents
wherein X represents a sulfur atom, Y represents a hydrogen, a lithium, a sodium, a potassium, a magnesium, a calcium or an aluminum atom; and p represents a valency of an atom represented by Y; -S-R2 (R2 represents a straight-chain alkyl group having from 9 to 25 carbon atoms or a branched alkyl group having from 4 to 25 carbon atoms, a straight-chain or a branched alkenyl group having from 3 to 25 carbon atoms, or a straight-chain or a branched alkynyl group having from 3 to 25 carbon atoms). In form of therapeutical compositions the compounds are effective against various diseases, including those caused by lipid deposition on the walls of blood vessels and cancer.