80729-06-2

Upstream product

• 64-17-5 ethanol 
• 98043-33-5 3-methylenecyclohex-2-enecarboxylic acid 
• 87362-45-6 ethyl 2-ethenyl-4-methyl-4-pentenoate 
• 80729-03-9 8-bromo-cis-5-methyl-6-oxabicyclo<3.2.1>octan-7-one 
• 861575-47-5 3-bromo-3-methyl-cyclohexanecarboxylic acid 

Downstream Products

• 24220-40-4 1-methyl-3-(α-oxy-isopropyl)-cyclohexene-(1) 
• 80729-05-1 3-methylcyclohex-2-en-1-ylmethanol 
• 80729-08-4 5,5-dimethyl-3-<(3-methyl-2-cyclohexenyl)methoxy>-2-cyclohexenone 

Relevant academic research and scientific papers

Intramolecular Photocycloaddition of the 3-(3-Butenyloxy)-2-cyclohexenone System

The irradiation of 5,5-dimethyl-3-(4-methyl-3-pentenyloxy)-2-cyclohexenone gave regioselectively, 6,6,10,10-tetramethyl-2-oxatricyclo1,5>undecan-8-one, while, that of 5,5-dimethyl-3--2-cyclohexenone afforded, regio- and stereoselectively, 1,5,5-trimethyl-8-oxatetracyclo2,7.01,5>tetradecan-3-one.

PALLADIUM DICHLORIDE-PROMOTED CYCLIZATIONS OF 1,5-DIENES. A NEW METHOD FOR FORMING CYCLOHEXENES.

1,5-Hexadienes, which are substituted with electron-withdrawing groups at carbon-3, undergo regioselective rearrangement to cyclohexenes upon treatment with palladium dichloride.