A solvent effect on the side‐chain conformation of phenylalanine derivatives and phenylalanine residuces in dipeptides

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Abstract
Three phenylalanine derivatives, Ac‐Phe‐NHMe, H‐Phe‐NHMe, and Ac‐Phe‐OH, were selected as models of Phe residues situated at the internal, the N‐terminal, and the C‐terminal positions of peptide chains, respctively. The side‐chain conformations of the three compounds were analyzed from the vicnal coupling constants 3JαβR and 3JαβS, of their 1H‐ nmr spectra measured in various organic sovlent. The two β‐protons were unambiguously assined by use of sterospecifically β‐monodeuterated phenylalanines. The pro‐S β‐proton was always situated at lower field than the pro‐R one when they were observed separately. The results of a solvent effect on the conformation of the tree compounds demonstrated that the rotamer populations are remarkable sensitive of the three compounds demonstrated that the rotamer populations are remarkably sensitive to solvent polarity and that the tendencies of the solvent effects are quite different from each other. Ac‐Phe‐OH Showed a trend similar to that of Ac‐Phe‐OEt reported by early workers. The rotamer populations of other derivatives (Ac‐Phe‐NMe2, Ac‐Phe‐NH2, Ac‐Phe‐OBut, and Ac‐Phe‐OBzl) and of Phe residues in some N‐acetyl dipeptde esters (Ac‐Phe‐Gly‐OMe, Ac‐Phe‐Val‐OMe, and Ac‐Gly‐Phe‐OMe) were also examined in several sovent, and it was found that substituents of the Phe carboxyl group—amides or esters—determine the tendency of the solvent effect. These results are interesting in the side‐chain conformations of Phe residues in peptides and proteins in an environment of low polarity can be disscussed on this experimental basis. Factors responsible for the solvent effect are discussed from (1) a structural comparison of the compunds with various carboxylic substituents, (2) an expriment with cyclohexylalanine derivatives, and (3) the measurement in mixed solvents wiht similar polarity.