86433-25-2Relevant academic research and scientific papers
Visible Light-Mediated Photochemical Reactions of 2-(2′-Alkenyloxy)cycloalk-2-enones
Gra?l, Raphaela,Jandl, Christian,Bach, Thorsten
, p. 11426 - 11439 (2020/10/12)
The title compounds were prepared, and their reactivity was studied upon sensitized irradiation at λ = 420 nm. Thioxanthen-9-one was employed as the sensitizer at a loading of 10 mol % in small-scale reactions and of 2.5 mol % on a larger scale. Cyclohex-
SYNTHESIS OF DIOSPHENOL ETHERS BY MEANS OF ALKOXYTRIMETHYLSILANES
Ponaras, A. A.,Meah, Md. Younus
, p. 4953 - 4956 (2007/10/02)
α-Diketones may be O-alkylated with a variety of alkoxytrimethylsilanes.
Process for the preparation of carbofuran
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, (2008/06/13)
A novel process is provided for the preparation of carbofuran and certain intermediate products. 1,2-Cyclohexanedione is alkylated with a beta-methallyl compound and the resulting product subjected to a Claisen rearrangement/aromatization to provide the c
Intramolecular Photocycloaddition of 2-(Alkenyloxy)cyclohex-2-enones
Ikeda, Masazumi,Takahashi, Masami,Uchino, Takamasa,Ohno, Kazunori,Tamura, Yasumitsu,Kido, Masaru
, p. 4241 - 4247 (2007/10/02)
Intramolecular photocycloaddition of 2-(2-propenyloxy)cyclohex-2-enones gave 2-oxabicyclohexane derivatives (head-to-tail adducts), and 2-(3-butenyloxy)cyclohex-2-enone afforded a 2-oxabicycloheptane derivative (a head-to-tail adduct) as the
