Alkynyl Sulfonium Salts Can Be Employed as Chalcogen‐Bonding Catalysts and Generate Alkynyl Radicals under Blue‐Light Irradiation
Chalcogen bonding (ChB) has emerged as a promising tool in organic synthesis. However, compared with the well‐developed selenium‐ and tellurium‐based salt catalysts, the ChB catalysis of sulfonium salts is still unknown. Here, we report a new type of alkynyl‐sulfonium salt ChB catalysis for various...
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Published in | Angewandte Chemie International Edition Vol. 61; no. 16; pp. e202116071 - n/a |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
WEINHEIM
Wiley
11.04.2022
Wiley Subscription Services, Inc |
Edition | International ed. in English |
Subjects | |
Online Access | Get full text |
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Summary: | Chalcogen bonding (ChB) has emerged as a promising tool in organic synthesis. However, compared with the well‐developed selenium‐ and tellurium‐based salt catalysts, the ChB catalysis of sulfonium salts is still unknown. Here, we report a new type of alkynyl‐sulfonium salt ChB catalysis for various ionic transformations, including transfer hydrogenation, bromination, bromolactonization, dimerization of 1,1‐diphenylethylene, nitro‐Michael addition reaction and Ritter reaction. More importantly, the photocapability of ChB was first demonstrated to generate alkynyl radicals for the synthesis of a variety of chalcogenoacetylenes. Mechanistic studies shed light on the mechanism of the photoinduced reactions and confirmed the involvement of alkynyl radicals which are difficult to generate otherwise.
Alkynyl sulfonium salts were employed as chalcogen bonding (ChB) catalysts for the first time. They display superior capability in the generation of alkynyl radicals under blue‐light irradiation. |
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Bibliography: | These authors contributed equally to this work. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1433-7851 1521-3773 1521-3773 |
DOI: | 10.1002/anie.202116071 |