(Q58103672)

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Synthesis of enantiomerically pure (3R,4R,5R)-4-hydroxy isoleucine lactone

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Synthesis of enantiomerically pure (3R,4R,5R)-4-hydroxy isoleucine lactone (English)

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Jean Martinez

6

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Tarek Kassem

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Jonhy Wehbe

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2

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Valérie Rolland-Fulcrand

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3

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Marc Rolland

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4

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Marie-Louise Roumestant

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5

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publication date

October 2001

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published in

Tetrahedron: Asymmetry

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volume

12

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issue

19

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page(s)

2657-2661

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cites work

[On the ingredients of the green amanita. XXVI. The building elements of gamma-amanitine]

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https://api.crossref.org/works/10.1016%2FS0957-4166%2801%2900465-7

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7 January 2021

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4-Hydroxyisoleucine from seed of Trigonella foenum-graecum

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Stereochemistry of the 4-hydroxyisoleucine from Trigonella foenum-graecum

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4-Hydroxyisoleucine: a novel amino acid potentiator of insulin secretion

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Some of the amino acid chemistry going on in the Laboratory of Amino Acids, Peptides and Proteins.

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Efficient asymmetric synthesis of amino acids through hydrogenation of the didehydroamino acid residue in cyclic imino-ester derivatives

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Enamino Ester Reduction: A Short Enantioselective Route to Pyrrolizidine and Indolizidine Alkaloids. Synthesis of (+)-Laburnine, (+)-Tashiromine, and (-)-Isoretronecanol

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10.1016/S0957-4166(01)00465-7

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(Q58103672)

Synthesis of enantiomerically pure (3R,4R,5R)-4-hydroxy isoleucine lactone

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