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Keywords = bis(4-methylbenzenesulfonate)

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7 pages, 1489 KB  
Communication
Tetramethyl 1,1′-(2-[{4,5-bis(Methoxycarbonyl)-1H-1,2,3-triazol-1-yl}methyl]-2-[(4-methylphenyl)sulfonamido]propane-1,3-diyl)bis(1H-1,2,3-triazole-4,5-dicarboxylate)
by Serigne Abdou Khadir Fall, Sara Hajib, Oumaima Karai, Younas Aouine, Salaheddine Boukhssas, Hassane Faraj and Anouar Alami
Molbank 2021, 2021(1), M1186; https://doi.org/10.3390/M1186 - 31 Jan 2021
Cited by 1 | Viewed by 3235
Abstract
A new compound tetramethyl 1,1′-(2-[{4,5-bis(methoxycarbonyl)-1H-1,2,3-triazol-1-yl}methyl]-2-[(4-methylphenyl)sulfonamido]propane-1,3-diyl)bis(1H-1,2,3-triazole-4,5-dicarboxylate) (3) was prepared in two steps starting from 2-((4-methylphenyl)sulfonamido)-2-((tosyloxy)methyl)propane-1,3-diylbis(4-methylbenzenesulfonate) (1), with an overall yield of 74%. The key step being the copper-free Huisgen cycloaddition between N [...] Read more.
A new compound tetramethyl 1,1′-(2-[{4,5-bis(methoxycarbonyl)-1H-1,2,3-triazol-1-yl}methyl]-2-[(4-methylphenyl)sulfonamido]propane-1,3-diyl)bis(1H-1,2,3-triazole-4,5-dicarboxylate) (3) was prepared in two steps starting from 2-((4-methylphenyl)sulfonamido)-2-((tosyloxy)methyl)propane-1,3-diylbis(4-methylbenzenesulfonate) (1), with an overall yield of 74%. The key step being the copper-free Huisgen cycloaddition between N-(1,3-diazido-2-(azidomethyl)propan-2-yl)-4-methylbenzenesulfonamide (2) and commercially available dimethyl acetylenedicarboxylate. The chemical structure of compound 3 was determined by IR, 1D and 2D NMR experiments, and elemental analysis. Full article
(This article belongs to the Collection Heterocycle Reactions)
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4 pages, 324 KB  
Short Note
3-Hydroxy-2-iodophenyl-(4-methylbenzenesulfonate)
by Feng Pan, Yi Guo, Jinying Shen, Xiaofeng Pan, Binbin Hu, Weixin Zheng, Jacques Maddaluno and Muriel Durandetti
Molbank 2020, 2020(4), M1158; https://doi.org/10.3390/M1158 - 6 Oct 2020
Cited by 1 | Viewed by 3112
Abstract
3-Hydroxy-2-iodophenyl-(4-methylbenzenesulfonate) was synthesized via a three-step procedure, starting from commercially available resorcinol, with an overall yield of 65%. The structures of the products were determined by 1H and 13C NMR, HRMS and IR. Full article
(This article belongs to the Section Organic Synthesis and Biosynthesis)
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