28509-24-2

Upstream product

• 630-19-3 pivalaldehyde 
• 381725-49-1 2-methoxy-5-(pyridin-2-yl)pyridine 
• 71-36-3 butan-1-ol 

Downstream Products

• 50270-27-4 2,4,6-trichloropyrimidine-5-carbaldehyde 
• 213316-32-6 (1S,2R)-1-amino-2-vinylcyclopropanecarboxylic acid ethyl ester 
• 138509-36-1 3-(3'-Cyclopentyloxy₄'-methoxy)phenyl-2-cyclohexene-1-one 
• 169280-16-4 2-methyl-2-phenyl-propionic acid , N-methoxy-N-methylamide 
• 169280-21-1 2-[4-(4-chloro-butyryl)-phenyl]-2-methyl-propionic acid 
• 121800-25-7 2-methyl-2-phenyl-propionic acid , dimethylamide 
• 177770-52-4 (2'S,2R,4S)acetic acid-2-[4-acetylamino-2-(4-chlorobenzyl)piperidin-1-yl]-2-oxo-1-phenyl ethyl ester 
• 77359-11-6 propanedioic acid mono[(4-nitrophenyl)methyl] ester 
• 169280-17-5 2-[4-(4-Chloro-butyryl)-phenyl]-2-methyl-propionic acid , dimethylamide 
• 364590-91-0 3-Chloro-benzo[b]thiophene-2-carboxylic acid (4'-cyano-6-methoxy-biphenyl-3-ylmethyl)-(4-methylaminocyclohexyl)-amide hydrochloride 
• 215303-07-4 2-Bromo-1-(3-Phenylpropyl)-4-(4-Fluorophenyl)-5-(4-Pyridyl)-1H-Imidazole 
• 19385-96-7 1,3?diamino?5,7?dimethyladamantane 

Relevant academic research and scientific papers

Reactivities of Carbonyl Compounds in Acid-Catalyzed Hydride Transfer vs. Electron Transfer

Rate constants for acid-catalyzed hydride-transfer reactions from triethylsilane to a series of carbonyl compounds are compared with those for acid-catalyzed electron transfer from the excited state of 2+ to the same series of carbonyl compounds in the presence of HClO4 in acetonitrile at 298 K.

1,2-DIHYDROPYRIDINE COMPOUNDS, PROCESS FOR PREPARATION OF THE SAME AND USE THEREOF

The present invention provides a novel compound having an excellent AMPA receptor inhibitory action and/or kainate inhibitory action. A compound represented by the following formula, a salt thereof or hydrates thereof. In the formula, Q indicates NH, O or S; and R1, R2, R3, R4 and R5 are the same as or different from each other and each indicates hydrogen atom, a halogen atom, a C1-6 alkyl group or a group represented by the formula -X-A (wherein X indicates a single bond, an optionally sbutituted C1-6 alkylene group etc.; and A indicates an optionally substituted C6-14 aromatic hydrocarbocyclic group or 5- to 14-membered aromatic heterocyclic group etc.).

Polymer-supported solution synthesis of oligosaccharides

The present invention provides improved syntheses of oligosacchairdes. In accordance with preferred embodiments, anomeric specificity in such syntheses can be attained using polymer-supported liquid synthetic design with certain novel diether linkers. The present invention also provides novel strategies for capping imcompletely glycosylated hydroxyls.