Easy access to α-carbonyl sulfones using cross-coupling of α-aryl-α-diazoesters with sulfonyl hydrazides

A facile synthesis of α-carbonyl sulfones has been accomplished by the cross-coupling of α-aryl-α-diazoesters with sulfonyl hydrazides in the presence of CuI and DBU. The reaction employs inexpensive and bench stable sulfonyl hydrazides as a sulfonyl source, and facilitates the migratory insertion w...

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Veröffentlicht in:Organic & biomolecular chemistry 2023-02, Vol.21 (5), p.987-993
Hauptverfasser: Sharma, Anup Kumar, Chand, Shiv, Kumar Pandey, Anand, Singh, Krishna Nand
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Sprache:eng
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Zusammenfassung:A facile synthesis of α-carbonyl sulfones has been accomplished by the cross-coupling of α-aryl-α-diazoesters with sulfonyl hydrazides in the presence of CuI and DBU. The reaction employs inexpensive and bench stable sulfonyl hydrazides as a sulfonyl source, and facilitates the migratory insertion with α-aryl-α-diazoesters under mild reaction conditions. Cu-catalyzed cross-coupling of α-aryl-α-diazoesters with sulfonyl hydrazides is explored to access α-carbonyl sulfones via migratory insertion of Cu-carbene species.
ISSN:1477-0520
1477-0539
DOI:10.1039/d2ob02219b