Author:
Wieland Theodor,Wehrt Hartmut,Dölling Jochen
Subject
Organic Chemistry,Physical and Theoretical Chemistry,General Medicine
Cited by
12 articles.
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1. 1,3-Dipolar cycloaddition of a chiral nitrone to (E)-1,4-dichloro-2-butene: a new efficient synthesis of (2S,3S,4R)-4-hydroxyisoleucine;Tetrahedron Letters;2012-06
2. A Practical and Efficient Total Synthesis of Potent Insulinotropic (2S,3R,4S)-4-Hydroxyisoleucine through a Chiral N-Protected γ-Keto-α-aminoester;European Journal of Organic Chemistry;2010-06-14
3. Multi-Step Synthesis and Biological Evaluation of Analogues of Insulin Secretagogue (2S,3R,4S)-4-Hydroxyisoleucine;European Journal of Organic Chemistry;2008-11-25
4. Analogues of insulin secretagogue (2S,3R,4S)-4-hydroxyisoleucine: synthesis by 1,3-dipolar cycloaddition reactions of chiral nitrones to alkenes;Tetrahedron: Asymmetry;2008-05
5. Synthesis of enantiomerically pure (3R,4R,5R)-4-hydroxy isoleucine lactone;Tetrahedron: Asymmetry;2001-10