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Tautomerism of carbothioic acids in aprotic media

✍ Scribed by S. T. Ioffe; Yu. N. Sheinker; M. I. Kabachnik


Book ID
112434724
Publisher
Springer
Year
1960
Tongue
English
Weight
735 KB
Volume
9
Category
Article
ISSN
1573-9171

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The syntheses, structure and reactivity of several boron derivatives of quinic acid, obtained in aprotic media, show that these boron heterocycles are useful intermediates, since they provide an alternative route to functionalize the quinic acid in a different way as when using dioxolane derivatives