(Q57572279)

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Substrate specificity of proline-4-hydroxylase: Chemical and enzymatic synthesis of 2S,3R,4S-epoxyproline

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Substrate specificity of proline-4-hydroxylase: Chemical and enzymatic synthesis of 2S,3R,4S-epoxyproline (English)

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Victor Lee

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Christopher J. Schofield

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6

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Christopher J. Schofield

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author name string

Jack E. Baldwin

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1

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Robert A. Field

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2

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Christopher C. Lawrence

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J.Kenneth Robinson

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5

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publication date

June 1994

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published in

Tetrahedron Letters

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volume

35

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issue

26

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page(s)

4649-4652

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cites work

The Preparation ofcis- andtrans-4-H3-L-Prolines and Their Use in Studying the Mechanism of Enzymatic Hydroxylation in Chick Embryos

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L-671,329, a new antifungal agent. II. Structure determination

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Proline 4-hydroxylase: Stereochemical course of the reaction

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Mechanism-based inactivation of thymine hydroxylase, an alpha-ketoglutarate-dependent dioxygenase, by 5-ethynyluracil

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Alternate substrates and inhibitors of bacterial 4-hydroxyphenylpyruvate dioxygenase

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Assay for 2-oxoglutarate decarboxylating enzymes based on the determination of [1-14C]succinate: application to prolyl 4-hydroxylase

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Reactions of 2-acyloxyisobutyryl halides with nucleosides. I. Reactions of model diols and of uridine.

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10.1016/S0040-4039(00)60753-0

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(Q57572279)

Substrate specificity of proline-4-hydroxylase: Chemical and enzymatic synthesis of 2S,3R,4S-epoxyproline

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