86236-18-2

Upstream product

• 106-96-7 propargyl bromide 
• 95-01-2 2,4-Dihydroxybenzaldehyde 

Downstream Products

• 1616487-87-6 (E)-1-(4,6-O-butylidene-β-D-glucopyranosyl)-4-{2,4-bis[1'-(dodecyl)-4'-hydroxymethylenetriazolo]phenyl}but-3-ene-2-one 
• 1616487-82-1 (E)-1-(4,6-O-butylidene-β-D-glucopyranosyl)-4-(2,4-bisprop-1’-oxo-2’-yne phenyl)-but-3-ene-2-one 
• 1616487-83-2 (E)-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-4-(2,4-bisprop-1’-oxo-2’-yne phenyl)-but-3-ene-2-one 

Relevant academic research and scientific papers

Benzaldehyde derivatives with functional propargyl groups as α-glucosidase inhibitors

The benzaldehyde derivatives (1–6) containing one and/or two propargyl arm(s) attached to the phenolic hydroxyl oxygen atom on the ortho-, meta- or para-positions of the aromatic ring were synthesized and characterized by spectral and microanalytical meth

Synthesis and characterization of novel phenoxy-substituted enediyne-triazole conjugates using click chemistry

Novel group of phenoxy-substituted enediyne-triazole conjugates were synthesized by Huisgen [3+2] cycloaddition reaction (Click chemistry) in aqueous media. It was observed that ene-diynes were stable in aqueous medium and open-air conditions.

Synthesis of novel 1,2,3-triazole based artemisinin derivatives and their antiproliferative activity

Two series of novel 1,2,3-triazole based artemisinin derivatives were designed, synthesized via a copper(i)-catalyzed azide alkyne cycloaddition (CuAAC) reaction and investigated for their antiproliferative activity by MTT assay against various human canc

Bis-triazologlycolipid mimetics - Low molecular weight organogelators

A facile regioselective synthesis of bis-triazologlycolipids, a class of organogelators, has been accomplished by "Click reaction". The morphology and self-assembly of the gelators were examined by FESEM and HRTEM analysis. the Partner Organisations 2014.

Syntheses and antibacterial activity of phendioxy substituted cyclic enediynes

Syntheses and antibacterial activity of 13-membered 1,3-phendioxy substituted cyclic enediynes are reported. The compounds were screened against gram-positive and gram-negative strains and some of the compounds exhibit potent antibacterial activity.