An Efficient Synthesis of N-Arylsulfonylindoles from Indoles and Arylsulfonyl Chlorides in the Presence of Triethyl-benzylammonium Chloride (TEBA) and NaOH
An efficient synthesis of N‐arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of triethylbenzylammonium chloride (TEBA) and NaOH at room temperature is described. An efficient synthesis of N‐arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of trie...
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Published in | Chinese journal of chemistry Vol. 28; no. 1; pp. 125 - 127 |
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Language | English |
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Weinheim
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ISSN | 1001-604X 1614-7065 |
DOI | 10.1002/cjoc.201090028 |
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Abstract | An efficient synthesis of N‐arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of triethylbenzylammonium chloride (TEBA) and NaOH at room temperature is described.
An efficient synthesis of N‐arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of triethylbenzylammonium chloride (TEBA) and NaOH at room temperature is described. |
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AbstractList | An efficient synthesis of N‐arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of triethylbenzylammonium chloride (TEBA) and NaOH at room temperature is described.
An efficient synthesis of N‐arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of triethylbenzylammonium chloride (TEBA) and NaOH at room temperature is described. An efficient synthesis of N ‐arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of triethylbenzylammonium chloride (TEBA) and NaOH at room temperature is described. An efficient synthesis of N-arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of triethylbenzylammonium chloride (TEBA) and NaOH at room temperature is described. |
Author | Wang, Yangyang Xu, Hui |
Author_xml | – sequence: 1 givenname: Hui surname: Xu fullname: Xu, Hui email: orgxuhui@nwsuaf.edu.cn organization: E-mail: orgxuhui@nwsuaf.edu.cn – sequence: 2 givenname: Yangyang surname: Wang fullname: Wang, Yangyang organization: Laboratory of Pharmaceutical Design & Synthesis, College of Science, Northwest Agriculture & Forestry University, Yangling, 712100 Shaanxi, China |
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Cites_doi | 10.1021/jo00350a001 10.1021/jo951520t 10.1248/cpb.56.1496 10.1021/jm00091a010 10.1021/jo00344a001 10.1021/jo060308u 10.1021/jm010943m 10.1021/jo990296v 10.1002/cjoc.200890266 10.1016/j.bmcl.2005.08.059 10.1016/S0960-894X(00)00453-4 10.1248/cpb.57.321 10.1248/cpb.57.797 |
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Snippet | An efficient synthesis of N‐arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of triethylbenzylammonium chloride (TEBA) and NaOH at... An efficient synthesis of N ‐arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of triethylbenzylammonium chloride (TEBA) and NaOH at... An efficient synthesis of N-arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of triethylbenzylammonium chloride (TEBA) and NaOH at... |
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SubjectTerms | Chlorides indole Indoles N-arylsulfonylindole phase transfer catalyst Sodium hydroxide triethylbenzylammonium chloride (TEBA) |
Title | An Efficient Synthesis of N-Arylsulfonylindoles from Indoles and Arylsulfonyl Chlorides in the Presence of Triethyl-benzylammonium Chloride (TEBA) and NaOH |
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