Synthesis of Fmoc-protected (2S,3S)-2-hydroxy-3-amino acids from a furyl substituted chiral cyanohydrin-Reference-Cited by-同舟云学术

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Synthesis of Fmoc-protected (2S,3S)-2-hydroxy-3-amino acids from a furyl substituted chiral cyanohydrin

Published:2003-06 Issue:12 Volume:14 Page:1645-1652
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Tromp Reynier A.,van der Hoeven Michael,Amore Alessia,Brussee Johannes,Overhand Mark,van der Marel Gijs A.,van der Gen Arne

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference41 articles.

1. Chemoenzymatic synthesis of Fmoc-protected (2S,3S)-2-hydroxy-3-amino acids and their application in the synthesis of an α-hydroxylated β-hexapeptide

2. β-AMINO ACIDS: MAMMALIAN METABOLISM AND UTILITY AS α-AMINO ACID ANALOGUES

3. Lithistid Sponges: Star Performers or Hosts to the Stars

4. THE DEVELOPMENT AND CLINICAL UTILITY OF THE TAXANE CLASS OF ANTIMICROTUBULE CHEMOTHERAPY AGENTS

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4. Cleavage and Formation of Cyanohydrins;Enzyme Catalysis in Organic Synthesis;2012-04-20

5. Hydroxynitrile Lyases: Insights into Biochemistry, Discovery, and Engineering;ACS Catalysis;2011-08-22

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