Iodine mediated/Brønsted acid-catalyzed dimerization of vinylarenes: a tandem reaction through Ritter trapping to produce N-(4-iodo-1,3-diarylbutyl) acetamides
| Autor: | Hong Zhu, Dong-Song Chen, Zhi-Jun Ye, Jing-Mei Huang |
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| Rok vydání: | 2012 |
| Předmět: |
Models
Molecular Vinyl Compounds Molecular Structure Organic Chemistry chemistry.chemical_element Stereoisomerism Trapping Alkenes Iodine Biochemistry Catalysis Styrene chemistry.chemical_compound Cascade reaction chemistry Yield (chemistry) Acetamides Organic chemistry Physical and Theoretical Chemistry Brønsted–Lowry acid–base theory Acids Dimerization |
| Zdroj: | Organic & Biomolecular Chemistry. 10:3610 |
| ISSN: | 1477-0539 1477-0520 |
| DOI: | 10.1039/c2ob25142f |
| Popis: | In the presence of p-toluenesulfonic acid and iodine, styrene derivatives undergo head-to-tail dimerization followed by trapping with nitriles to yield the corresponding Ritter-type products. |
| Databáze: | OpenAIRE |
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