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Catalyst‐ and Light‐free S−H Insertion between Phosphorodithioic Acids and Diazo Compounds: Rapid Access to Dialkylphosphorodithioates
A catalyst‐ and light‐free S−H insertion of phosphorodithioic acids with diazo compounds has been developed, in which phosphorodithioic acid acts not only as an acid promoter but also as a nucleophile. This protocol features fast reaction rate, broad substrate scope, mild conditions, and simple oper...
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Published in: | Asian journal of organic chemistry 2023-07, Vol.12 (7), p.n/a |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A catalyst‐ and light‐free S−H insertion of phosphorodithioic acids with diazo compounds has been developed, in which phosphorodithioic acid acts not only as an acid promoter but also as a nucleophile. This protocol features fast reaction rate, broad substrate scope, mild conditions, and simple operation, providing a cost‐effective and general approach to diverse phosphorodithioates.
A catalyst‐ and light‐free S−H insertion between the phosphorodithioic acids with diazo compounds has been developed, where the phosphorodithioic acid acts not only as an acid promoter but also as a nucleophile. |
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ISSN: | 2193-5807 2193-5815 |
DOI: | 10.1002/ajoc.202300053 |