Novel keto–enol tautomerism in 1,3,5-trihydroxybenzene systems
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We report a new synthesis of the water-soluble compound 1,3,5-trihydroxy-2,4,6-trimethylsulfonic acid (1), which exists in two tautomeric forms (60 : 40::enol%:keto%), and its lanthanide complexes. Relative tautomer stability is influenced by intramolecular H-bonding and competing implicit solvent effects.
2016 ◽
Vol 511
(1)
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pp. 630-637
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1973 ◽
Vol 28
(9-10)
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pp. 590-594
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2019 ◽
Vol 24
(9)
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pp. 1133-1143
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2000 ◽
Vol 17
(1)
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pp. 13-28
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1997 ◽
Vol 157
(1)
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pp. 43-52
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