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3,3,3-Trifluoro-2-isocyanopropionates, new versatile building blocks for the introduction of trifluoromethyl groups into organic molecules [1]
British Library Online Contents | 1993| -
Peptide modification by incorporation of -trifluoromethyl -amino acids via trifluoromethyl-substituted acylimines
British Library Online Contents | 1993| -
2-Trifluoromethyl-Substituted Amino Acids, 20. - Incorporation of -Trifluoromethyl-Substituted -Amino Acids into the N- and C-Terminal Position of Azapeptides
British Library Online Contents | 1994| -
Peptide modification by incorporation of α-trifluoromethyl α-amino acids via trifluoromethyl-substituted acylimines
National licenceElsevier | 1992| -
3,3,3-Trifluoro-2-isocyanopropionates, new versatile building blocks for the introduction of trifluoromethyl groups into organic molecules (1)
Online Contents | 1994|Contributors: Schierlinger, C. -
2-Trifluoromethyl-substituted amino acids, 19-2-Trifluoromethyl a-Amino acid esters, building blocks for trifuoromethyl-substituted ureas, thioureas and other potential biological active structures
Online Contents | 1994|Contributors: Schierlinger, C. -
2-Trifluoromethyl-substituted amino acids, 20. - Incorporation of a-trifluoromethyl-substituted a-amino acids into the N- and C-terminal position of azapeptides
Online Contents | 1994|Contributors: Schierlinger, C. -
Peptide modification by incorporation of a-trifluoromethyl a-amino acids via trifluoromethyl-substituted acylimines
Online Contents | 1993|Contributors: Schierlinger, C.
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