74266-80-1Relevant articles and documents
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
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.