An efficient chemomicrobiological synthesis of stable isotope-labeled L-tyrosine and L-phenylalanine
- 1 April 1986
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 51 (8) , 1175-1179
- https://doi.org/10.1021/jo00358a004
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
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- Synthesis of [3',5'-13C2]tyrosine and its use in the synthesis of specifically labeled tyrosine analogs of oxytocin and arginine vasopressin and their 2-D-tyrosine diastereoisomersThe Journal of Organic Chemistry, 1979
- Synthesis of specific deuterium labeled tyrosine and phenylalanine derivatives and their use in the total synthesis of [8-arginine]vasopressin derivatives: the separation of diastereomeric [8-arginine]vasopressin derivatives by partition chromatographyJournal of the American Chemical Society, 1977
- Selectively deuterated amino acid analogues synthesis, Incorporation into proteins and NMR propertiesBiochimica et Biophysica Acta (BBA) - General Subjects, 1977