Synthesis of (5R,6R,7S)-6-iodo-1,5,6,7-tetrahydro-4,1-benzoxazonin-3(2H)-ones
New 6-iodo-1,5,6,7-tetrahydro-3H-4,1-benzoxazonin-3-ones have been synthesized by reaction of N-tosyl- and N-(2-nitrobenzenesulfonyl)-N-[2-(alkenyl)phenyl]aminoacetic acids with molecular iodine.
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
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
Reactions of N-and C-alkenylanilines: X.* Synthesis of 2-vinyldihydroindoles from 4-methyl-2-(pent-3-en-2-yl)aniline
2-(1-Iodoethyl)-3,5-dimethyl-1-(4-methylphenylsulfonyl)-2, 3-dihydro-1H-indole reacted with pyridine, piperidine, N-alkylpiperidines, and dimethylformamide to give dehydrohalogenation and halogen substitution products whose ratio depended on the reagent s
Mazgarova, G. G.,Absalyamova, A. M.,Gataullin, R. R.
p. 1200 - 1209,10
(2020/10/15)
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