Nucleophilic Aromatic Substitution on 4-Fluorophenylsulfonamides: Nitrogen, Oxygen, and Sulfur Nucleophiles
Abstract Improved conditions are reported for the stoichiometric reaction of nitrogen, oxygen, and sulfur nucleophiles with weakly activated 4-fluorophenylsulfonamides.
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Veröffentlicht in: | Synlett 2005-02, Vol.2005 (3), p.449-452 |
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container_issue | 3 |
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container_title | Synlett |
container_volume | 2005 |
creator | Badetti, Elena Moreno-Mañas, Marcial Pleixats, Roser Sebastián, Rosa M. Serra, Anna Soler, Roger Vallribera, Adelina |
description | Abstract
Improved conditions are reported for the stoichiometric reaction of nitrogen, oxygen, and sulfur nucleophiles with weakly activated 4-fluorophenylsulfonamides. |
doi_str_mv | 10.1055/s-2005-862363 |
format | Article |
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Improved conditions are reported for the stoichiometric reaction of nitrogen, oxygen, and sulfur nucleophiles with weakly activated 4-fluorophenylsulfonamides.</abstract><doi>10.1055/s-2005-862363</doi><tpages>4</tpages></addata></record> |
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title | Nucleophilic Aromatic Substitution on 4-Fluorophenylsulfonamides: Nitrogen, Oxygen, and Sulfur Nucleophiles |
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