Oxidative trifluoromethylthiolation and thiocyanation of amines: a general approach to N–S bond formation

Literature Information

Publication Date 2016-03-16
DOI 10.1039/C6QO00064A
Impact Factor 5.281
Authors

Heng-Ying Xiong, Xavier Pannecoucke, Tatiana Besset


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Abstract

Herein, we described a practical and efficient one-pot oxidative trifluoromethylthiolation of amines. A panel of primary and secondary amines was functionalized in good yields at room temperature. This general approach was further applied to the thiocyanation of anilines and the corresponding products can be readily used as SCN electrophilic sources.

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Additions and Corrections

Front/Back Matter

DOI: 10.1039/C4PY90054E

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Organic Chemistry Frontiers

Organic Chemistry Frontiers
CiteScore: 7.8
Self-citation Rate: 8.7%
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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