93322-81-7Relevant articles and documents
Atropoisomerism in Hindered Naphthyl Sulfoxides: Structure, Stereodynamics, and Chiral Resolution
Casarini, D.,Foresti, E.,Gasparrini, F.,Lunazzi, L.,Macciantelli, D.,et al.
, p. 5674 - 5682 (1993)
Barriers for the E,Z interconversion of atropisomers of 1-naphthyl sulfoxides (ArSOR) having a methyl group at position 2 of the naphthalene moiety were measured by variable-temperature NMR.Their values were found to cover the range 10.6-18.4 kcal molsup
Fragmentation of anion radicals with elimination of aryloxy groups
Dneprovskii,Fedosov
, p. 1438 - 1443 (2007/10/03)
4-Vinylbenzyl phenyl ether, 4-phenylbenzyl phenyl ether, 1- and 2-naphthylmethyl phenyl ethers react with sodium thiophenolate under photochemical stimulation with replacement of the phenoxy group. The composition of reaction products and relation of reactivity to the structure of substrates is consistent with anion-radical mechanism. The corresponding methoxy and cyano derivatives do not undergo the reaction.