106180-60-3

Upstream product

• 934-20-3 (2Z)-2-(hydroxymethylene)cycloheptanone 
• 502-42-1 cycloheptanone 
• 106180-33-0 1-Ethynyl-2-[1-isopropoxy-meth-(Z)-ylidene]-cycloheptanol 
• 106180-27-2 2-Ethynyl-1-cycloheptene-carboxaldehyde 
• 65519-66-6 2-(Isopropoxymethylene)-cycloheptanone 
• 5798-79-8 bromo-phenyl-acetonitrile 
• 106180-41-0 (Z)-3-(2-Ethynyl-1-cycloheptenyl)-2-phenyloxirane-2-carbonitrile 

Relevant academic research and scientific papers

Antiparasitic Agents: Part VI-Synthesis of 7-Chloro-4-(4-substituted-phenylamino)- and 7-Chloro-4-(4-substituted-piperazin-1-yl)quinolines as Potential Antiparasitic Agents

The synthesis of a series of 7-chloro-4-(4-hydroxy-3-substituted-phenylamino)quinolines (9-13, 31-40, 58) and 7-chloro-4-(4-substituted-piperazin-1-yl)quinolines (41-51, 53-55) has been carried out.These compounds have been tested for their antimalarial,

THERMALLY INITIATED REACTIONS OF (Z)-EPOXYHEXENYNES A FACILE PREPARATION OF 3,4-ANNULATED FURANS

An efficient and general access to 3,4-annulated 2-vinylfurans (type II) is provided by the thermally induced ring transformation of epoxyhexenynes (I).Depending on the substitution pattern the reactions proceed either by heating in solution (5a-h) or under short-time thermolysis conditions (6i, j).The results are consistent with a multistep mechanism involving 1-oxacyclohepta-3,4,6-trienes as central intermediates.