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10Audrey L. Stokes, Shigeki J. Miyake-Stoner, Jennifer C. Peeler, Duy P. Nguyen, Robert P. HammerscCurrent address: New England Peptide, 65 Zub Lane, Gardner, MA 01420, USA. and Ryan A. Mehl.
Enhancing the utility of unnatural amino acidsynthetases by manipulating broad substrate specificity, Mol. Biosyst., 2009, 5, 1032. Synthesis of a decapeptide fragment of ribonuclease (64u201373), Chemistry of Natural Compounds Control of Neural Cell Adhesion on 3D-SWCNT, Multiscale Fabrication of Functional Materials for Regenerative Medicine New hydrogenation catalyst: An advantageous method for the removal of hydrogenolysable protecting groups in peptide synthesis, Letters in Peptide Science New hydrogenation catalyst: An advantageous method for the removal of hydrogenolysable protecting groups in peptide synthesis, Letters in Peptide Science Lubell, W. D.; Blankenship, J. W.; Fridkin, G.; Kaul, R., Science of Synthesis, (2005) 21, 735..
Benzyl Group, Science of Synthesis