TY - JOUR
T1 - Benzoquionones and related compounds. Part 2.1 Preferred conformations of some acyl-1,4-benzoquinones in solution
AU - Bruce, J. Malcolm
AU - Heatley, Frank
AU - Ryles, Roderick G.
AU - Scrivens, James
PY - 1980/1/1
Y1 - 1980/1/1
N2 - Studies based on polarographic reduction potentials, electronic absorption spectra, and 1H and 13C 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.
AB - Studies based on polarographic reduction potentials, electronic absorption spectra, and 1H and 13C 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.
UR - http://www.scopus.com/inward/record.url?scp=0006327013&partnerID=8YFLogxK
U2 - 10.1039/P29800000860
DO - 10.1039/P29800000860
M3 - Article
AN - SCOPUS:0006327013
SN - 1470-1820
SP - 860
EP - 866
JO - Journal of the Chemical Society, Perkin Transactions 2
JF - Journal of the Chemical Society, Perkin Transactions 2
IS - 6
ER -