50344-32-6

Upstream product

• 22966-19-4 trans-4'-methoxychalcone 
• 120-92-3 cyclopentanone 
• 959-23-9 4'-methoxychalcone 

Downstream Products

• 73669-94-0 2-(4-Methoxy-phenyl)-4-phenyl-octahydro-cyclopenta[b]thiopyran 
• 73669-84-8 Trifluoro-acetate2-(4-methoxy-phenyl)-4-phenyl-6,7-dihydro-5H-cyclopenta[b]thiopyranylium; 
• 92744-74-6 2-Phenyl-4-(p-methoxyphenyl)-1,9a-trimethylene-9-oxa-4a-aza-1,2,4a,9a-tetrahydrofluorene 
• 92744-84-8 2-Phenyl-9a-(p-methoxyphenyl)-3,4-trimethylene-9-oxa-4a-aza-1,2,4a,9a-tetrahydrofluorene 

Relevant academic research and scientific papers

Domino products from the reaction of 1,3-diaryl-2-propen-1-ones (chalcones) with cyclopentanone

The simple reaction of chalcones with cyclopentanone in the presence of barium hydroxide furnished complex domino products of the types 4 and 5 along with 1,5-diketones 3. Mechanistic considerations reveal that the bicyclic alcohol 4 was formed by sequent

DIRECTION OF HETEROCYCLIZATION IN THE INTERACTION OF SEMICYCLIC 1,5-DIKETONES WITH BIFUNCTIONAL NUCLEOPHILES

In the interaction of a series of 1-aryl-3-R-3-(2'-oxo-cycloalkyl)-1-propanones with o-aminophenol and o-phenylenediamine, depending on the structure of the reacting compounds, derivatives of 1,9a-tetra(tri)-methylene-9-oxa(aza)-4a-aza-1,2,4a,9a-tetrahydrofluorene are formed.The interaction of 1-(o-hydroxyphenyl)- and 1-(o-aminophenyl)-3-R-3-(2'-oxocycloalkyl)-1-propanones with o-aminophenol, o-phenylenediamine, ethanolamine, and ethylenediamine leads to the formation of new heterocyclic systems: 2,7-dioxa-5-azatricyclo1,5>dodecane, 7-oxa-2,5-diazatricyclo1,5>dodecane, and 2,5,7-triazatricyclo1,5>dodecane.