ISSN:
1476-4687
Source:
Nature Archives 1869 - 2009
Topics:
Biology
,
Chemistry and Pharmacology
,
Medicine
,
Natural Sciences in General
,
Physics
Notes:
[Auszug] The four isoleucine stereoisomers are shown in Fig. 1 as are their interconversion pathways by epimerization at the a- and -carbons. The a-epimerization rates of D-Ile and L-alle would be expected to be similar to those of the diastereomeric pair L-Ile and D-alle. Interconversion of the enantiomers ...
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1038/319314a0
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