A synthesis of C-glycosidic multivalent mannosides suitable for divergent functionalized conjugation
摘要:
Divergent synthesis of two novel C-glycosidic multivalent mannosides derived from a common trivalent C-mannosyl carboxylate-terminated intermediate is described. This illustrates synthesis of multivalent C-glycosidic architectures bearing variable extended functionalized tethers. One such tether incorporates an embedded fluorescent unit providing a C-mannosyl multivalent epitope offering potential applications through further conjugation or immobilization. (C) 2011 Elsevier Ltd. All rights reserved.
Visible-Light-Mediated Organocatalyzed Thiol–Ene Reaction Initiated by a Proton-Coupled Electron Transfer
作者:Vitalij V. Levin、Alexander D. Dilman
DOI:10.1021/acs.joc.9b01331
日期:2019.6.21
A convenient method for performing a thiol–ene reaction is described. The reaction is performed under blue-light irradiation and catalyzed by photoactive Lewis basic molecules such as acridine orange or naphthalene-fused N-acylbenzimidazole. It is believed that the process is initiated by a proton-coupled electron transfer process within the complex between the thiol and the Lewis basic catalyst.
[EN] STABLE VACCINE AGAINST CLOSTRIDIUM DIFFICILE<br/>[FR] VACCIN STABLE DIRIGÉ CONTRE CLOSTRIDIUM DIFFICILE
申请人:VAXXILON AG
公开号:WO2020104697A1
公开(公告)日:2020-05-28
The present invention relates to a synthetic saccharide of general formula (I) that is related to Clostridium difficile PS-II cell-surface polysaccharide and conjugate thereof. Said synthetic saccharide, said conjugate and pharmaceutical composition containing said synthetic saccharide or said conjugate are useful for prevention and/or treatment of diseases associated with Clostridium difficile. Furthermore, the synthetic saccharide of general formula (I) is useful as marker in immunological assays for detection of antibodies against Clostridium difficile bacteria.
generation of thiylradicals via hole oxidation to initiate the reaction, followed by redox neutral pathway and/or chain transfer pathway to accomplish thiol–olefin coupling. It is notable that CsPbBr3 exhibits advanced thiol-ene performance than that using MHP analogs and others. The work presents a new exploration of MHP-mediated transformation and shows great potential of MHPs for radical chemistry
The present invention relates to a synthetic saccharide of general formula (I) that is related to Klebsiella pneumoniae serotype O1, O2, O2ac, and O8 O-polysaccharide and carbapenem-resistant Klebsiella pneumoniae ST258 O-polysaccharide and conjugate thereof. Said synthetic saccharide, said conjugate and pharmaceutical composition containing said synthetic saccharide or said conjugate are useful for prevention and/or treatment of diseases associated with Klebsiella pneumoniae. Furthermore, the synthetic saccharide of general formula (I) is useful as marker in immunological assays for detection of antibodies against Klebsiella pneumoniae bacteria.
Reductions with Metal Hydrides. XV. Reduction of 2-Tetrahydropyranyl and 2-Tetrahydrofuranyl Thioethers with Lithium Aluminum Hydride- Aluminum Chloride
作者:Ernest L. Eliel、Bernard E. Nowak、Ronald A. Daignault