Results 241 to 250 of about 12,676 (308)
Oxidative benzylic C(sp<sup>3</sup>)-H functionalisation of electron-poor substrates with photoexcited DDQ. [PDF]
Atkins AP +8 more
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<i>O</i>-Trifluoromethylation of ketones: an alternative straightforward route to alkenyl trifluoromethyl ethers. [PDF]
Gao C +6 more
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Highly-Selective Electrochemical Decarboxylative Late-Stage Functionalization of Amino Acids. [PDF]
Ghosh A +4 more
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Photoreactions of benzonitrile with cyclic enol ethers
Abstract Upon irradiation, cyclic enol ethers such as 1-methoxy-cyclopentene (4) mainly add across the cyano group of benzonitrile (1), under formation of 2-azabutadienes of an imidoester type. This is in agreement with the so-called Δ G-correlation which was reported earlier (ref. 5 and 6).
Mattay, Jochen +3 more
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The photoalkylation of cyclic ethers
Tetrahedron, 1967Abstract The acetone, acetophenone and benzophenone-initiated photochemical alkylation of cyclic ethers with olefins is described. Alpha-alkylated cyclic ethers were obtained as the 1:1-adducts in yields of up to 40% with terminal olfeins, and yields of up to 82% with α,β-unsaturated esters.
I. Rosenthal, D. Elad
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Dilithiated Synthons: Synthesis of Cyclic Ethers.
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
F. Alonso, J. Meléndez, M. Yus
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