Journal
GREEN SYNTHESIS AND CATALYSIS
Volume 2, Issue 4, Pages 385-388Publisher
KEAI PUBLISHING LTD
DOI: 10.1016/j.gresc.2021.10.001
Keywords
Borane-catalysed; Diazoester; S-H insertion; Thiophenols; Thiols; C-S bond Formation
Categories
Funding
- National Natural Science Foundation of China [21971066, 21772042]
- Science and Technology Commis- sion of Shanghai Municipality [18JC1412300]
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The novel B(C6F5)3-catalysed S-H bond insertion reaction provides a convenient and efficient method for synthesizing sulfides in moderate to excellent yield under mild conditions. This approach features simple operation, broad substrate scope, and easy scale-up, offering an alternative to transition-metal catalysed reactions.
Herein, we have developed a novel B(C6F5)3-catalysed S-H bond insertion of thiophenols and thiols with & alpha;-aryl-& alpha;-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.
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