Acyl cyanides have been shown to behave as carbonyl dienophiles in reactions with electron-rich o-quinodimethanes. This represents the first observation of an acyl cyanide carbonyl group reacting in such a manner.
CHARLTON, J. L.;DURST, T., TETRAHEDRON LETT., 1984, 25, N 25, 2663-2666
作者:CHARLTON, J. L.、DURST, T.
DOI:——
日期:——
DURST, T.;KOZMA, E. C.;CHARLTON, J. L., J. ORG. CHEM., 1985, 50, N 24, 4829-4833
作者:DURST, T.、KOZMA, E. C.、CHARLTON, J. L.
DOI:——
日期:——
Photochemical synthesis of α-oxygenated benzothiophenedioxides
作者:James L. Charlton、Tony Durst
DOI:10.1016/s0040-4039(01)81257-0
日期:1984.1
Stereoselectivity in the Diels-Alder reaction of phenyl- and oxy-substituted o-quinodimethanes
作者:Tony Durst、Elisabeth C. Kozma、James L. Charlton