100867-36-5Relevant academic research and scientific papers
Electrochemical-In-Situ-Oxidative Sulfonylation of Phenols with Sulfinic Acids as an Access to Sulfonylated Hydroquinones
Sun, Xue,Zhang, Fanjun,Yan, Kelu,Feng, Wenfeng,Sun, Xuejun,Yang, Jianjing,Wen, Jiangwei
supporting information, p. 3485 - 3490 (2021/06/17)
The electrochemical in-situ oxidative sulfonylation of phenols with sulfinic acids access to sulfonylated hydroquinones has been developed. A series of sulfonylated hydroquinones were prepared under mild mediator-, catalyst- and exogenous-oxidant-free con
Ammonium iodide-promoted unprecedented arylsulfonylation of quinone with sodium arylsulfinates
Yuan, Jin-Wei,Liu, Shuai-Nan,Qu, Ling-Bo
, p. 6763 - 6772 (2017/10/26)
A novel ammonium iodide-promoted arylsulfonylation of quinones with sodium arylsulfinates has been explored. This reaction proceeded smoothly through unique nucleophilic addition reaction and produced the arylsulfonylation products in moderate to good yields. The reactions proceeded efficiently over a broad range of substrates with good regioselectivity and functional group tolerance.
Synthesis and biological evaluation of novel sulfonyl-naphthalene-1,4-diols as FabH inhibitors
Alhamadsheh, Mamoun M.,Waters, Norman C.,Sachdeva, Sarbjot,Lee, Patricia,Reynolds, Kevin A.
supporting information; experimental part, p. 6402 - 6405 (2009/09/30)
A series of analogs of 2-tosylnaphthalene-1,4-diol were prepared and were found to be potent 10-20 nM reversible inhibitors of the Escherichia coli FabH enzyme. The inhibitors were also effective but to a lesser degree (30 nM-5 μM), against the Mycobacter
