Journal of the Chemical Society. Perkin transactions II p. 860 - 866 (1980)
Update date:2022-07-30
Topics:
Bruce, Malcolm
Heatley, Frank
Ryles, Roderick G.
Scrivens, James H.
Studies based on polarographic reduction potentials, electronic absorption spectra, and (1)H and (13)C nuclear magnetic relaxation data show that in solution the preferred conformation of formyl-1,4-benzoquinone is that with the formyl and quinonoid groups coplanar, and the formyl carbonyl group anti to the 1-carbonyl, whereas that of acetyl- and pivaloyl-1,4-benzoquinone has the acyl groups approximately perpendicular to the quinonoid ring.
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Doi:10.1016/S0022-1139(00)82509-9
(1974)Doi:10.1039/c39790000846
(1979)Doi:10.1021/jo049385k
(2004)Doi:10.1021/ic049600f
(2004)Doi:10.1023/B:COHC.0000008264.35326.20
(2003)Doi:10.1016/S0040-4039(00)71456-0
(1980)
