20131-81-1

Upstream product

• 19073-14-4 4-(1,3-dioxolan-2-yl)aniline 
• 79-22-1 methyl chloroformate 
• 2403-53-4 2-(4-nitrophenyl)-1,3-dioxolane 
• 67-56-1 methanol 
• 2597-44-6 formyl radical 
• 555-16-8 4-nitrobenzaldehdye 
• 30063-17-3 4-[(methoxycarbonyl)amino]benzoic acid 
• 1341397-27-0 methyl (4-(hydroxymethyl)phenyl)carbamate 
• 150-13-0 4-amino-benzoic acid 
• 556-18-3 4-aminobenzaldehyde 
• 6294-89-9 hydrazinecarboxylic acid methyl ester 
• 52161-21-4 N-[4-(1,3-dioxolan-2-yl)phenyl]acetamide 

Downstream Products

• 89221-65-8 [4-(3-Methyl-oxazolidin-2-yl)-phenyl]-carbamic acid methyl ester 
• 87623-02-7 [4-(4-Methyl-[1,3]dioxolan-2-yl)-phenyl]-carbamic acid methyl ester 
• 87641-98-3 (4-[1,3]Dioxepan-2-yl-phenyl)-carbamic acid methyl ester 
• 81263-12-9 [4-(4-Methyl-[1,3]dioxan-2-yl)-phenyl]-carbamic acid methyl ester 
• 87537-46-0 (4-{[(E)-2-Hydroxy-ethylimino]-methyl}-phenyl)-carbamic acid methyl ester 
• 87622-91-1 2-(4'-methoxycarbamino)phenyldioxane-1,3 
• 87623-20-9 2-(4'-methoxycarbamino)phenyl-dithiolane-1,3 
• 89221-80-7 (4-{[(E)-2-Dimethylamino-ethylimino]-methyl}-phenyl)-carbamic acid methyl ester 
• 84832-84-8 (4-Thiazolidin-2-yl-phenyl)-carbamic acid methyl ester 
• 81263-10-7 2-(4'-methoxycarbamino)phenyloxathiolane-1,3 
• 87623-09-4 (4-[1,3]Dioxan-2-yl-phenyl)-carbamic acid methyl ester 
• 87623-06-1 [4-(4,5-Dimethyl-[1,3]dioxolan-2-yl)-phenyl]-carbamic acid methyl ester 
• 87537-51-7 [4-(3-Methylcarbamoyl-oxazolidin-2-yl)-phenyl]-carbamic acid methyl ester 
• 71207-60-8 [4-(3-Methylcarbamoyl-thiazolidin-2-yl)-phenyl]-carbamic acid methyl ester 

Relevant academic research and scientific papers

Copper-Catalyzed Coupling of Amines with Carbazates: An Approach to Carbamates

A new approach for the preparation of carbamatesviathe copper-catalyzed cross-coupling reaction of amines with alkoxycarbonyl radicals generated from carbazates is described. This environmentally friendly protocol takes place under mild conditions and is compatible with a wide range of amines, including aromatic/aliphatic and primary/secondary substrates.

FACTOR XIa INHIBITORS

The present invention provides a compound of Formula (I) and pharmaceutical compositions comprising one or more said compounds, and methods for using said compounds for treating or preventing thromboses, embolisms, hypercoagulability or fibrotic changes. The compounds are selective Factor XIa inhibitors or dual inhibitors of Factor XIa and plasma kallikrein.

Efficient palladium/1,10-phenanthroline-catalyzed reductive carbonylation of mono- and dinitroarenes to urethanes in phosphonium salt ionic liquids

(Chemical Equation Presented) The highly reactive and selective reductive carbonylation of mono- and dinitroarenes to the corresponding mono- and diurethanes was carried out in the presence of a PdCl2/Phen catalytic system, using PSIL110[C14H29(C6H 13)3P+PF6-] as the ionic liquid under mild reaction conditions. No cocatalyst is required.

New pesticides and intermediates. Part VI. Some 2-substituted dioxa-, oxathio-, and dithiocyclanes

N-Formylphenyl and N-acetophenyl derivatives of urea and carbamic acid (1) were reacted with diols and their sulfur analogs to yield easily the title compounds (2-9).