95539-05-2Relevant articles and documents
Stereoselectivity in the Diels-Alder Reaction of Phenyl- and Oxy-Substituted o-Quinodimethanes
Durst, Tony,Kozma, Elisabeth C.,Charlton, James L.
, p. 4829 - 4833 (2007/10/02)
Phenyl-, methoxy-, and acetoxy-substituted o-quinodimethanes (o-QDM) have been added to dimethyl fumarate and maleate to determine the stereoselectivity of the addition reaction.The o-QDM's were generated from the corresponding 1,3-dihydrobenzothiophen
PHOTOCHEMICAL SYNTHESIS OF α-OXYGENATED BENZOTHIOPHENEDIOXIDES
Charlton, James L.,Durst, Tony
, p. 2663 - 2666 (2007/10/02)
The photochemical synthesis of 1-hydroxybenzo-1,3-dihydrothiophene-2,2-dioxides from orthomethylbenzaldehyde and its analogs is described.Some of the chemistry of these α-oxygenated sulfones, including exchange of the 1-hydroxy group with various alkox
o-Quinodimethanes from 3,6-Dihydrobenzo-1,2-oxanthiin-2-oxides
Charlton, James L.,Durst, Tony
, p. 5287 - 5290 (2007/10/02)
A two step synthesis of 3,6-dihydrobenzo-1,2-oxanthiin-2-oxide 5a from o-tolualdehyde via the photochemically produced 1-hydroxy-1,3-dihydrobenzothiophene-2,2-dioxide is described.Analoguos syntheses of 3 and 6 substituted derivatives of the benzosu