In vitro conversion of leucine to valine: configurational assignment of [5-13C]leucines
Author:
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi00522a039
Reference16 articles.
1. Stereochemistry of the reductoisomerase and αβ-dihydroxyacid dehydratase-catalysed steps in valine and isoleucine biosynthesis. Observation of a novel tertiary ketol rearrangement
2. Use of chiral isopropyl groups in biosynthesis. Synthesis of (2RS,3S)-[413C]-valine
3. Oxidations involving silver. II. The oxidation of alcohols and aldehydes with silver(II) picolinate
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1. Synthesis of 13C/D Doubly Labeled l-Leucines: Probes for Conformational Analysis of the Leucine Side-chain;The Journal of Organic Chemistry;2001-07-31
2. Three approaches to the synthesis of L-leucine selectively labelled with carbon-13 or deuterium in either diastereotopic methyl group;Journal of the Chemical Society, Perkin Transactions 1;2000
3. Stereoselective deuterium-labelling of diastereotopic methyl and methylene protons of L-leucine;Tetrahedron Letters;1998-03
4. Stereospecific synthesis of (2S,4R)-[5,5,5-2H3]leucine;Journal of the Chemical Society, Perkin Transactions 1;1996
5. METHODS FOR THE SYNTHESIS OF L-LEUCINE SELECTIVELY LABELED WITH C-13 OR DEUTERIUM IN EITHER DIASTEREOTOPIC METHYL-GROUP;TETRAHEDRON LETT;1995
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