The synthesis of daidzein sulphates

Brian Fairley; Nigel P. Botting; Aedin Cassidy

doi:10.1016/S0040-4020(03)00869-X

The synthesis of daidzein sulphates

Brian Fairley
, Nigel P. Botting
, Aedin Cassidy

Research output: Contribution to journal › Article

34 Citations (Scopus)

Abstract

The first syntheses of the urinary isoflavone metabolites, daidzein 4'-sulfate, daidzein 7-sulfate and daidzein 4',7-disulfate are described. These syntheses employ a key protecting group strategy, allowing regiospecific sulfation.

Original language	English
Pages (from-to)	5407-5410
Number of pages	4
Journal	Tetrahedron
Volume	59
Issue number	29
DOIs	https://doi.org/10.1016/S0040-4020(03)00869-X
Publication status	Published - 14 Jul 2003

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10.1016/S0040-4020(03)00869-X

Cite this

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title = "The synthesis of daidzein sulphates",

abstract = "The first syntheses of the urinary isoflavone metabolites, daidzein 4'-sulfate, daidzein 7-sulfate and daidzein 4',7-disulfate are described. These syntheses employ a key protecting group strategy, allowing regiospecific sulfation.",

author = "Brian Fairley and Botting, \{Nigel P.\} and Aedin Cassidy",

year = "2003",

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day = "14",

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language = "English",

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AU - Fairley, Brian

AU - Botting, Nigel P.

AU - Cassidy, Aedin

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N2 - The first syntheses of the urinary isoflavone metabolites, daidzein 4'-sulfate, daidzein 7-sulfate and daidzein 4',7-disulfate are described. These syntheses employ a key protecting group strategy, allowing regiospecific sulfation.

AB - The first syntheses of the urinary isoflavone metabolites, daidzein 4'-sulfate, daidzein 7-sulfate and daidzein 4',7-disulfate are described. These syntheses employ a key protecting group strategy, allowing regiospecific sulfation.

U2 - 10.1016/S0040-4020(03)00869-X

DO - 10.1016/S0040-4020(03)00869-X

M3 - Article

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SP - 5407

EP - 5410

JO - Tetrahedron

JF - Tetrahedron

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