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Iodine-catalyzed oxidative system for 3-sulfenylation of indoles with disulfides using DMSO as oxidant under ambient conditions in dimethyl carbonate
The iodine catalyzed oxidative system for 3-sulfenylation of indoles with disulfides using DMSO as oxidant has been achieved under ambient conditions, providing a convenient and efficient method for the synthesis of 3-sulfenylindoles in good to excellent yields and with high selectivity. The reactio...
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Published in: | Green chemistry : an international journal and green chemistry resource : GC 2012-01, Vol.14 (7), p.2066-2070 |
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container_end_page | 2070 |
container_issue | 7 |
container_start_page | 2066 |
container_title | Green chemistry : an international journal and green chemistry resource : GC |
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creator | Ge, Wenlei Wei, Yunyang |
description | The iodine catalyzed oxidative system for 3-sulfenylation of indoles with disulfides using DMSO as oxidant has been achieved under ambient conditions, providing a convenient and efficient method for the synthesis of 3-sulfenylindoles in good to excellent yields and with high selectivity. The reaction was carried out in a green solvent, DMC, under atmospheric conditions. Only 0.5 mmol of disulfide was needed for the 3-sulfenylation of 1 mmol of indole because both the sulfenyl groups of a symmetric disulfide take part in the reaction. The procedure is suitable for N-protected or unprotected indoles. |
doi_str_mv | 10.1039/c2gc35337g |
format | article |
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The reaction was carried out in a green solvent, DMC, under atmospheric conditions. Only 0.5 mmol of disulfide was needed for the 3-sulfenylation of 1 mmol of indole because both the sulfenyl groups of a symmetric disulfide take part in the reaction. The procedure is suitable for N-protected or unprotected indoles.</description><identifier>ISSN: 1463-9262</identifier><identifier>EISSN: 1463-9270</identifier><identifier>DOI: 10.1039/c2gc35337g</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Catalysis ; Chemistry ; Exact sciences and technology ; General and physical chemistry ; Heterocyclic compounds ; Heterocyclic compounds with only one n hetero atom and condensed derivatives ; Organic chemistry ; Preparations and properties ; Theory of reactions, general kinetics. Catalysis. 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The reaction was carried out in a green solvent, DMC, under atmospheric conditions. Only 0.5 mmol of disulfide was needed for the 3-sulfenylation of 1 mmol of indole because both the sulfenyl groups of a symmetric disulfide take part in the reaction. The procedure is suitable for N-protected or unprotected indoles.</description><subject>Catalysis</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Heterocyclic compounds</subject><subject>Heterocyclic compounds with only one n hetero atom and condensed derivatives</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><subject>Theory of reactions, general kinetics. Catalysis. 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source | Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list) |
subjects | Catalysis Chemistry Exact sciences and technology General and physical chemistry Heterocyclic compounds Heterocyclic compounds with only one n hetero atom and condensed derivatives Organic chemistry Preparations and properties Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
title | Iodine-catalyzed oxidative system for 3-sulfenylation of indoles with disulfides using DMSO as oxidant under ambient conditions in dimethyl carbonate |
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