Matches in SemOpenAlex for { <https://semopenalex.org/work/W4211180916> ?p ?o ?g. }
- W4211180916 endingPage "80" @default.
- W4211180916 startingPage "31" @default.
- W4211180916 abstract "Condensation between D-glucose and boric acid in acetone, in the presence of a strong-acid catalyst, gives the discrete, cyclic ester 1,2-O-isopropylidene-α-D-glucofuranose 3,5-borate. It can be used in the preparation of 6-substituted derivatives of D-glucose. This chapter provides an overview of the progress made in the field of carbohydrate boronates. The chapter describes two methods of synthesis of boronates—namely, the direct condensation of carbohydrates with boronic acids and the other method that includes synthesis from borinates. Chemical methods for determining boronate structures usually involve the substitution of unesterified hydroxyl groups, and the characterization of the products, either by examination of the compounds obtained after removal of the boronate groups, or by independent synthesis of the fully substituted compounds by boronation of known derivatives. The most useful physical methods of structural analysis, apart from X-ray diffraction, are nuclear magnetic resonance (n.m.r.) spectroscopy and mass spectrometry. Newer applications of 13C- and 11B-n.m.r. spectroscopy indicate the value in the determination of the ring size of boronates." @default.
- W4211180916 created "2022-02-13" @default.
- W4211180916 creator A5033545183 @default.
- W4211180916 date "1978-01-01" @default.
- W4211180916 modified "2023-10-11" @default.
- W4211180916 title "Carbohydrate Boronates" @default.
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- W4211180916 doi "https://doi.org/10.1016/s0065-2318(08)60218-8" @default.