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Complementary strategies for synthesis of sulfinamides from sulfur-based feedstock
We describe a straightforward one-pot reductive protocol for the synthesis of sulfinamides from sulfonyl chlorides. This method enables the preparation of sulfinamides with a broad range of functional groups. Furthermore, we have expanded a known oxidative pathway to sulfinamides starting from thiol...
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Published in: | Organic & biomolecular chemistry 2023-04, Vol.21 (14), p.295-2954 |
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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: | We describe a straightforward one-pot reductive protocol for the synthesis of sulfinamides from sulfonyl chlorides. This method enables the preparation of sulfinamides with a broad range of functional groups. Furthermore, we have expanded a known oxidative pathway to sulfinamides starting from thiols. These methods together provide a general strategy for the synthesis of sulfinamides from common sulfur-based feedstock that is available with large structural and functional group diversity.
We describe a straightforward one-pot reductive protocol for the synthesis of sulfinamides from sulfonyl chlorides. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/d3ob00050h |