35355-33-0Relevant articles and documents
Substituent effect on the photochemistry of 4,4-dialkoxylated- and 4-hydroxylated cyclohexenones
Chen, Yu-Jen,Wang, Hui-Ling,Villarante, Nelson R.,Chuang, Gary Jing,Liao, Chun-Chen
, p. 9591 - 9599 (2013/10/22)
Photochemistry of the title compounds in various solvents was studied using a broad band of light centered at 350 nm. C-4 spiroketal cyclohexenone 4 (1.0 M) afforded dimers and 12b with the predominance of the former in polar solvent and the latter in non
Formal syntheses of (±)-methylenomycins A and B
Hong, Fang-Tsao,Lee, Kung-Shing,Liao, Chun-Chen
, p. 77 - 83 (2007/10/03)
The syntheses of methyl ester of (±)-desepoxy-4,5-didehydromethylenomycin A (4) and 2,3-dimethyl-5-methoxycarbonyl-2-cyclopentenone (5) were accomplished from a common starting material, 2,3-dimethyl-4-methoxyphenol (8), in only four and two steps in 35%