Synthesis of N-Tosyl Triazole 2a:2-(1-tosyl-1H-1,2,3 triazol-4-yl)phenyl Methanol
3:03
Synthesis of N-(2-alkoxyvinyl)sulfonamide Phthalan 3a: (Z)-N-(isobenzofuran-1(3H)-ylidenemethyl)-4-methylbenzenesulfonamide
4:14
Synthesis of Phthalan 4: N-((1,3-dihydroisobenzofuran-1-yl)methyl)-4-methylbenzenesulfonamide
5:34
Synthesis of Phenylthylamine 5: N-(2-(hydroxymethyl)phenethyl)-4-methylbenzenesulfonamide
7:29
Synthesis of Ketal 6c: N-((1-(2-hydroxyethoxy)-1,3-dihydroisobenzofuran-1-yl)methyl)-4-methybenzenesulfonamide
8:12
Results: Characterization of N-(2-alkoxyvinyl)sulfonamides and Derivatives
10:00
Conclusion
副本
The overall goal of this report is to demonstrate an efficient methodology for accessing N-2-alkoxy vinyl sulfonamides, a synthetically versatile functional group, and to illustrate several reactions that convert this group into valuable heterocyc
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Representative experimental procedures for the synthesis of N-(2-alkoxyvinyl)sulfonamides and subsequent conversion to phthalan and phenethylamine derivatives are presented in detail.