87947-46-4Relevant articles and documents
Diels–Alder trapping vs. amidoalkylation of cyclopentadiene with polychloroacetaldehyde sulfonylimines
Chernysheva, Gulnur N.,Katerinich, Maxim D.,Rozentsveig, Igor B.,Ushakov, Igor A.
, p. 618 - 620 (2020/10/09)
The reaction of chloral or dichloro(phenyl)acetaldehyde N-arylsulfonylimines with cyclopentadiene, depending on the reaction conditions, affords either Diels–Alder adducts, 2-arylsulfonyl-2-azabicyclo[2.2.1]hept-5-enes, or unexpectedly new amidoalkylated
SINGLE-STAGE SYNTHESIS OF N-ARYLSULFONYL-SUBSTITUTED 1,2,3,6-TETRAHYDROPYRIDINES AND 2-AZABICYCLOHEPT-5-ENES
Mirskova, A. N.,Gogoberidze, I. T.,Levkovskaya, G. G.,Kalikhman, I. D.,Bannikova, O. B.,et al.
, p. 1547 - 1550 (2007/10/02)
The reaction of trichloroethylidenearenesulfonamides with the formula CCl3CH=NSO2C6H4X (X=H, Cl, CH3), obtained in a single stage from trichloroethylene and N,N-dichloroarenesulfonamides, with piperylene and isoprene leads to N-arylsulfonyl-2-trichloromet