Photochemical synthesis. VI. The formation of benzosemibullvalene derivatives in the photoaddition of diphenylacetylene to methyl 2-naphthoate, a degenerate thermal isomerization of the benzosemibullvalene skeleton.
Sugowdz G, et al.
Australian Journal of Chemistry, 26(1), 147-171 null
Stereochemistry of a cubane-like photodimer of methyl 2-naphthoate.
Lei L, et al.
Tetrahedron Letters, 47(27), 4725-4727 (2006)
Cucurbit [8] uril-mediated photodimerization of alkyl 2-naphthoate in aqueous solution.
Lei L, et al.
Tetrahedron Letters, 49(9), 1502-1505 (2008)
Molecular association of singlet excited state methyl 2-naphthoate; effects of excimer formation on photocycloaddition.
Chow YL and Johansson CI.
Research on Chemical Intermediates, 19(3), 191-209 (1993)
Journal of mass spectrometry : JMS, 53(5), 379-384 (2018-02-15)
Gas phase decompositions of protonated methyl benzoate and its conjugates have been studied by using electrospray ionization-collision induced dissociation-tandem mass spectrometry. Loss of CO2 molecule, thus transfer of methyl group, has been observed. In order to better understand this process
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