83191-34-8Relevant academic research and scientific papers
Synthesis of (1′S*,2R*,3R*)- and (1′S*,2R*,3S*)-N-arylsulfonyl-2-(1′-halogenethyl)-3-methylindolines and their selective toxicity against SH-SY5Y cell line
Gataullin, Rail R.,Maksimova, Marina A.,Vakhitova, Yuliya V.,Zainullina, Liana F.,Zileeva, Zulfia R.
, (2020/01/24)
N-tosyl-2- and N-tosyl-4-halogen-substituted derivatives of 2-(1-methylbut-2-en-1-yl)aniline were synthesized and their molecular iodine-mediated cyclization was investigated. The cyclization upon interaction of N-tosyl-6-methyl-2-(1-methylbut-2-en-1-yl)a
Synthesis of 6-methyl-4-(1-methyl-2-buten-1-yl)-2-(2-cyclohexen-1-yl)- and 6-methyl-4-(1-methyl-2-buten-1-yl)-2-(1-cyclohexen-1-yl)anilines
Gataullin,Ishberdina,Sotnikov,Abdrakhmanov
, p. 438 - 440 (2008/02/01)
Alkenylation of 6-methyl-2-(2-cyclohexen-1-yl)- and 2-(1-cyclohexen-1-yl)anilines with piperylene in the presence of AlCl 3 and transformation of the resulting cyclohexenylanilines into carbazole structures were studied.
Reactions of N- and C-alkenylanilines: III. Synthesis and cyclization of substituted 2-(1-methyl-2-butenyl)anilines
Gataullin,Minnigulov,Fatykhov,Spirikhin,Abdrakhmanov
, p. 31 - 37 (2007/10/03)
Reactions of substituted 2-(1-methyl-2-butenyl)anilines with iodine result in cyclization and formation of 3-iodo-1,2,3,4-tetrahydroquinolines; N-methylsulfonyl-2-(1-methyl-2-butenyl)anilines give rise exclusively to the corresponding 2-(1-iodoethyl)-3-methyl-2,3-dihydroindoles.
Alkenylation of anilines with dicyclopentadiene, cyclopentadiene, and piperylene
Gataullin,Kazhanova,Sagitdinov,Galyautdinov,Fatykhov,Spirikhin,Abdrakhmanov
, p. 280 - 285 (2007/10/03)
Alkenylation of anilines with dicyclopentadiene, cyclopentadiene, and piperylene in the presence of mineral acids and Lewis acids was studied.
ACID-CATALYZED RERRANGEMENT OF N-(1-METHYL-2-BUTENYL)ANILINE
Abdrakhmanov, I.B.,Sharafutdidov, V.M.,Tolstikov, G.A.
, p. 562 - 564 (2007/10/02)
The effect of the nature of the solvents and catalysts on the rerrangement of N-(1-methyl-2-butenyl)aniline was studied..The reaction is catalyzed by the hydrochlorides of aromatic amines and by Lewis acids.The nature of the solvents has an insignificant effect on the course of the rearrangement.
AMINO-CLAISEN REARRANGEMENT AS A METHOD FOR THE SYNTHESIS OF C-SUBSTITUTED ANILINES
Abdrakhmanov, I. B.,Sharafutdinov, V. M.,Nigmatullin, N. G.,Sagitdinov, I. A.,Tolstikov, G. A.
, p. 1278 - 1283 (2007/10/02)
Various C-alkenylanilines were synthesized by an amino-Claisen rearrangement.The composition of the rearrangement products is affected by the nature of the substituents in the benzene ring and at the nitrogen atom of the initial anilines.
