103348-78-3Relevant articles and documents
A mild method for generation of p-methoxybenzyl cation through NIS- mediated activation of p-methoxybenzyl 4-pentenyl ether
Okada,Kitagawa,Fujita,Taguchi
, p. 8135 - 8142 (1996)
A mild and facile method for generation of p-methoxybenzyl cation through NIS-mediated activation of p-methoxybenzyl 4-pentenyl ether was achieved. Under the present activation conditions, various alcohols were convened to the corresponding p-methoxybenzyl ethers. A scope and limitation of the present p-methoxybenzylation reaction was also investigated.
Heterocyclization involving benzylic C(sp3)-H functionalization enabled by visible light photoredox catalysis
Pandey, Ganesh,Laha, Ramkrishna,Mondal, Pradip Kumar
, p. 9689 - 9692 (2019/08/15)
A general and efficient method for heterocyclization involving benzylic C(sp3)-H functionalization enabled by visible light photoredox catalysis to access a wide range of structurally diverse oxygen as well as nitrogen heterocycles up to a gram scale is reported. The potential application of this new methodology is demonstrated by the total synthesis of (-)-codonopsinine and (+)-centrolobine. Herein it is proposed that selectfluor, unlike a fluorinating reagent, acts as an oxidative quencher and a hydrogen radical acceptor.
PdII-katalysierte regioselektive Arylchlorierung und Oxyarylierung ungesaettigter Alkohole
Tamaru, Yoshinao,Hojo, Makoto,Higashimura, Hideyuki,Yoshida, Zen-ichi
, p. 740 - 742 (2007/10/02)
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