143994-16-5Relevant academic research and scientific papers
The bioinspired design of a reagent allows the functionalization of Cα-H of α,β-unsaturated carbonyl compounds via the Baylis-Hillman chemistry under ambient conditions
Singh, Palwinder,Kumar, Arun,Kaur, Sukhmeet,Kaur, Jagroop,Singh, Harpreet
supporting information, p. 2936 - 2939 (2016/02/20)
A rationally designed reagent capable of affecting alkylation at Cα of α,β-unsaturated carbonyl compounds is reported. The reaction proceeded at room temperature without any additives. The pH and H-bond formation during the reaction play a key role in the working of the reagent.
Furan-2(3H)- and 2(5H)-ones. Part 5. Photoreaction of 3-Benzylfuran-2(5H)-ones; Cyclisation to Indenofuranones
Muraoka, Osamu,Tanabe, Genzoh,Sano, Kyohko,Minematsu, Toshie,Momose, Takefumi
, p. 1833 - 1846 (2007/10/02)
The effect of substitution at the 'central methane' on the photoreactivity of 3-benzylfuran-2(5H)-ones 5a-g was investigated.Despite its di-?-methane structure, photochemical arylation was effected to give substituted indenofuranones 6 in good yields.Only
A BREAKTHROUGH FOR THE PHOTOCHEMICAL ARYLATION IN THE 3-(PHENYLMETHYL)-2(5H)-FURANONE SYSTEM LEADING TO THE TETRAHYDROINDENOFURANONE SYSTEM
Muraoka, Osamu,Tanabe, Genzoh,Sano, Kyohko,Momose, Takefumi
, p. 1093 - 1096 (2007/10/02)
The photochemistry of the 'central methane'-substituted 3-benzyl-2(5H)-furanone system (1) is described.Despite its di-?-methane structure, photochemical arylation was found to predominate in place of the di-?-methane rearrangement, and gave substituted t
