Reduction of 4-oxo α-amino acids as a route to 4-hydroxylated α-amino acids. Concise approaches to the synthesis of clavalanine, erythro-4-hydroxyornithine and (+)-bulgecinine
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1994/P1/P19940001719
Reference47 articles.
1. Preparation of enantiomerically pure protected 4-oxo .alpha.-amino acids and 3-aryl .alpha.-amino acids from serine
2. Preparation of enantiomerically pure protected unsaturated α-amino acids from a new serine derived zinc–copper reagent
3. Reactions of a Serine-derived Zinc/Copper Reagent with Tricarbonyl(cyclohexadienyl) Iron Salts: Synthesis of Protected Amino Acids
4. An Approach to the Synthesis of Enantiomerically Pure Hydroxylated α-Amino Acids Using Zinc Homoenolate Chemistry
5. Short, stereoselective syntheses of 4,5,6-trihydroxylated norleucines: An approach to the synthesis of (+)-bulgecinine
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