Methods for the Synthesis of L-Leucine Selectively Labelled with Carbon-13 or Deuterium in either Diastereotopic Methyl Group
- 6 November 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (45) , 8315-8318
- https://doi.org/10.1016/0040-4039(95)01738-4
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Chemo-enzymatic syntheses of isotopically labelled L-amino acidsTetrahedron Letters, 1994
- Synthesis of (2S,4S)- and (2S,4R)-[5,5,5-2H3] leucine from (R)-pulegoneCanadian Journal of Chemistry, 1994
- Methods for the synthesis of α‐keto estersRecueil des Travaux Chimiques des Pays-Bas, 1993
- Stereospecific synthesis of (2S,4R)-[5,5,5-2H3]-leucineTetrahedron Letters, 1992
- Synthesis and properties of the .alpha.-keto acidsChemical Reviews, 1983
- Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivativesJournal of the American Chemical Society, 1982
- In vitro conversion of leucine to valine: configurational assignment of [5-13C]leucinesBiochemistry, 1981
- Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolatesJournal of the American Chemical Society, 1981
- Pattern of incorporation of leucine samples asymmetrically labelled with 13C in the isopropyl unit into the C5-isoprenoid units of echinuline and flavoglaucineJournal of the Chemical Society, Chemical Communications, 1977