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https://doi.org/10.1016/s0040-4039(00)84943-6
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Cite Journal: Tetrahedron Letters |  Publication Date: Jan 1, 1986 |
 Citations: 19 |
Affiliation: Tokyo University of Science
Use of dimethylphosphinyl (Dmp) group as a side-chain phenolic OH protecting group of tyrosine in peptide synthesis was studied. The Dmp group is resistant to trifluoroacetic acid and hydrogenolysis and removed by fluoride ion or liquid HF.
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