Abstract:Simple access to aryl sulfinates from aryl iodides and bromides is reported using an inexpensive Ni‐electrocatalytic protocol. The reaction exhibits a broad scope, uses stock solution of simple SO2 as sulfur source, and can be scaled up in batch and recycle flow settings. The limitations of this reaction are clearly shown and put into context by benchmarking with state‐of‐the‐art Pd‐based methods.
“…Looking at organic chemistry we notice a tremendous growth of interest in the development of novel electrochemical methodologies. Ackermann, [1][2][3][4] Baran, [5][6][7][8] Lin, 9,10 Mei, [11][12][13] Waldvogel [14][15][16] and many other eminent scientists have proverbially brought electrosynthesis/electrocatalysis to light by turning it into a perfectly working synthetic tool. [17][18][19][20][21][22][23][24][25][26][27][28][29][30][31][32] This, in turn, has many implications for the development of materials chemistry.…”
Occasionally, there appears a synthetic strategy, in which virtues are so manifest, that it seems to be a game changer. Not long ago, scientists intensively explored mechanochemistry, ionic liquids, and...
“…Looking at organic chemistry we notice a tremendous growth of interest in the development of novel electrochemical methodologies. Ackermann, [1][2][3][4] Baran, [5][6][7][8] Lin, 9,10 Mei, [11][12][13] Waldvogel [14][15][16] and many other eminent scientists have proverbially brought electrosynthesis/electrocatalysis to light by turning it into a perfectly working synthetic tool. [17][18][19][20][21][22][23][24][25][26][27][28][29][30][31][32] This, in turn, has many implications for the development of materials chemistry.…”
Occasionally, there appears a synthetic strategy, in which virtues are so manifest, that it seems to be a game changer. Not long ago, scientists intensively explored mechanochemistry, ionic liquids, and...
We have developed an electrochemical method for the direct C−H sulfonylation of aldehyde hydrazones using sodium sufinates as the sulfonylating agent under supporting electrolyte-free conditions. This straightforward sulfonylation strategy afforded a library of (E)-sufonylated hydrazones with high tolerance of various functional groups. The radical pathway of this reaction has been revealed by the mechanistic studies.Letter pubs.acs.org/OrgLett
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