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<i>N</i>-Sulfonylbenzotriazoles as Advantageous Reagents for <i>C</i>-Sulfonylation
45
Citations
58
References
2005
Year
Diversity Oriented SynthesisDerivativesEngineeringHeterocyclicNatural SciencesDiversity-oriented SynthesisAlpha-cyanoalkyl Sulfones 5A-iAvailable N-Organic ChemistryCatalysisSynthetic ChemistryChemistryHeterocycle ChemistryPharmacologyAdvantageous ReagentsDerivative (Chemistry)Alpha-sulfonyl Acids 14A-c
[Structure: see text]. Reactions of readily available N-(alkyl-, aryl-, and heteroarylsulfonyl)benzotriazoles 3a-h with diverse nitriles, reactive heteroaromatics, alkylheteroaromatics, sulfones, and esters produced alpha-cyanoalkyl sulfones 5a-i, sulfonylheteroaromatics 7a-e, alpha-(sulfonylalkyl)heterocycles 9a-f, alpha-sulfonylalkyl sulfones 11a-g, and esters of alpha-sulfonyl acids 14a-c, respectively, in synthetically useful to excellent yields. The results represent the first examples of the successful application of sulfonylazoles for C-sulfonylation.
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