461672-48-0Relevant articles and documents
Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime ethers: XIV.* halogenation of N-[arylsulfonylimino(phenyl)methyl]-2,5- dialkyl-1,4-benzoquinone monoimines and their reduction products
Avdeenko,Konovalova,Ledeneva,Santalova,Pirozhenko,Palamarchuk,Shishkin
, p. 928 - 937 (2012/11/07)
Despite steric hindrances created by the bulky substituent on the nitrogen atom, halogenation of 2,5-dialkyl-N-[arylsulfonylimino(phenyl)methyl]-1,4- benzoquinone monoimines fairly readily gives their derivatives having two halogen atoms in the quinoid ring. Pleiades Publishing, Ltd., 2012.
Hydrohalogenation of N-[arylsulfonylimino(phenyl)methyl]-1,4-benzoquinone monoimines having alkyl substituents in the quinoid ring
Avdeenko,Konovalova,Pirozhenko,Ledeneva,Santalova
experimental part, p. 1035 - 1044 (2011/11/14)
Hydrohalogenation of N-[arylsulfonylimino(phenyl)methyl]-2,5(3,5)-dimethyl- 1,4-benzoquinone monoimines follows exclusively the 1,4-addition pattern, whereas N-[arylsulfonylimino(phenyl)methyl]-2,6-dimethyl-1,4-benzoquinone monoimines take up hydrogen halides according to the 6,3-addition scheme.
Thiocyanation of N-arylsulfonyl-, N-aroyl-, and N-[(N-arylsulfonyl) benzimidoyl]-1,4-benzoquinone imines
Avdeenko,Pirozhenko,Konovalov,Roman'Kov,Palamarchuk,Shishkinc
experimental part, p. 408 - 416 (2009/09/06)
Reactions of thiocyanate ion with N-aroyl-, N-arylsulfonyl-, and N-(N-arylsulfonylbenzimidoyl)-1,4-benzoquinone imines follow the 1,4-addition pattern, and the adducts undergo intramolecular cyclization to give the corresponding N-substituted 5-amino-1,3-