136869-44-8Relevant articles and documents
Diels-alder trapping of ortho-quinone methides. A new entry to substituted xanthene- 1,4-diones
Giraud, Luc,Giraud, Anne
, p. 1153 - 1160 (2007/10/03)
Highly regioselective Diels-Alder reactions of a non-protected β-hydroxy quinone have been achieved after formation of chelated lithium alkoxides. In this report, we demonstrate on a model system, that the selectivity of reactions based on 1,3-dioxy-subst
Fluoride as leaving group in SRN1 reactions of a tetrasubstituted-1,4-benzoquinone
Crozet, Michel P.,Giraud, Luc,Sabuco, Jean-Francois,Vanelle, Patrice
, p. 1063 - 1064 (2007/10/02)
2-Fluoromethyl-3,5,6-trimethyl-1,4-benzoquinone was synthesized and its reactivity in SRN1 reactions compared to the reactivity of the chloro derivative previously described. This study reports the first examples of the displacement of the fluoride in SRN1 reactions involving a substitution at an sp3 carbon atom.