Stereospecific synthesis of (2S,4R)-[5,5,5-2H3]-leucine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Stereospecific assignment of the methyl1H NMR lines of valine and leucine in polypeptides by nonrandom13C labelling
2. Stereospecific nuclear magnetic resonance assignments of the methyl groups of valine and leucine in the DNA-binding domain of the 434 repressor by biosynthetically directed fractional carbon-13 labeling
3. 1H And 13C NMR chemical shifts of the diastereotopic methyl groups of valyl and leucyl residues in peptides and proteins
4. Pattern of incorporation of leucine samples asymmetrically labelled with 13C in the isopropyl unit into the C5-isoprenoid units of echinuline and flavoglaucine
5. On the mode of incorporation of leucine samples labelled at positions 5 and 2 with 3H and 14C into the isoprenylated tryptophan derivative echinuline from
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