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Volumn 2, Issue 1, 2000, Pages 29-32

N-arylation of sulfonamides on solid supports

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EID: 0001997073     PISSN: 15204766     EISSN: None     Source Type: Journal    
DOI: 10.1021/cc9900394     Document Type: Article
Times cited : (31)

References (19)
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    • note
    • Copper salts could not be completely washed from the resin after the reaction, but they could be easily resin-quenched from the cleaved material using Chelex resin and the product filtered off. Although polystyrene resin was used for all the syntheses described, we later found that the copper salts were more easily washed away from PEG resins. The N-arylation yields were similar for PEG and PS resins.
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    • Piscopio, A. D.; Miller, J. F.; Koch, K. A Second Generation Solid-Phase Approach to Freidinger Lactams: Application of Fukuyama's Amine Synthesis and Cyclative Release via Ring Closing Metathesis. Tetrahedron Lett. 1998, 39, 2667-2670. Fukuyama, T.; Jow, C.; Cheung, M. 2- and 4-Nitrobenzenesulfonamides: Exceptionally Versatile Means for Preparation of Secondary Amines and Protection of Amines. Tetrahedron Lett. 1995, 36, 6373-6374.
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