Borane-catalysed S–H insertion reaction of thiophenols and thiols with α-aryl-α-diazoesters
Herein, we have developed a novel B(C6F5)3-catalysed S–H bond insertion of thiophenols and thiols with α-aryl-α-diazoesters under mild conditions, furnishing various sulfides in moderate to excellent yield. This method features simple operation, mild conditions, broad substrate scope and easy scale-...
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Published in | Green synthesis and catalysis Vol. 2; no. 4; pp. 385 - 388 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.11.2021
KeAi Communications Co. Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | Herein, we have developed a novel B(C6F5)3-catalysed S–H bond insertion of thiophenols and thiols with α-aryl-α-diazoesters under mild conditions, furnishing various sulfides in moderate to excellent yield. This method features simple operation, mild conditions, broad substrate scope and easy scale-up, which provide an alternative approach for transition-metal catalysed reaction.
Herein, we have developed a novel B(C6F5)3-catalysed S–H bond insertion of thiophenols and thiols with α-aryl-α-diazoesters under mild condition, furnishing various sulfides in moderate to excellent yield. This method features simple operation, mild conditions, broad substrate scope and easy scale-up, which provide alternative approach for transition-metal catalysed reaction. [Display omitted] |
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ISSN: | 2666-5549 2666-5549 |
DOI: | 10.1016/j.gresc.2021.10.001 |