Indexed keywords
ACIDS;
AMINATION;
AMINO ACIDS;
ORGANIC ACIDS;
ALDEHYDES;
COMBINATORIAL CHEMISTRY;
HOMOLOGOUS SERIES;
ORTHOGONAL PROTECTION;
OXIME;
PEPTIDE LINKERS;
PEPTIDE SYNTHESIS;
PEPTIDOMIMETIC;
SIDE CHAINS;
AMINES;
3 [(DIPHENYL 4 TOLYLMETHYL)AMINOOXYL N [[(9H FLUOREN 9 YL METHYL)OXY]CARBONYL]SERINE;
3 CARBOXY 10,10 DIMETHYL 8 OXO 6,9 DIOXA 2,7 DIAZA DECANOIC ACID 1 (9H FLUOREN 9 YLMETHYL)ESTER;
3 CARBOXY 11,11 DIMETHYL 9 OXO 7,10 DIOXA 2,7 DIAZA DECANOIC ACID 1 (9H FLUOREN 9 YLMETHYL)ESTER;
3 CARBOXY 12,12 DIMETHYL 10 OXO 8,11 DIOXA 2,9 DIAZA DECANOIC ACID 1 (9H FLUOREN 9 YLMETHYL)ESTER;
3 CARBOXY 13,13 DIMETHYL 11 OXO 8,12 DIOXA 2,10 DIAZA DECANOIC ACID 1 (9H FLUOREN 9 YLMETHYL)ESTER;
3 CARBOXY 14,14 DIMETHYL 12 OXO 10,13 DIOXA 2,11 DIAZA DECANOIC ACID 1 (9H FLUOREN 9 YLMETHYL)ESTER;
3 CARBOXY 9,9 DIMETHYL 7 OXO 5,8 DIOXA 2,6 DIAZA DECANOIC ACID 1 (9H FLUOREN 9 YLMETHYL)ESTER;
AMINO ACID DERIVATIVE;
PEPTIDE LIBRARY;
AMINO ACID ANALYSIS;
AMINO ACID SYNTHESIS;
ARTICLE;
CHEMICAL STRUCTURE;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
SYNTHESIS;
1
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2 followed by reduction of the resulting double bond during under the reducing conditions of resin cleavage using triethylsilane.
2 followed by reduction of the resulting double bond during under the reducing conditions of resin cleavage using triethylsilane.
23
49649099338
The major fraction obtained by HPLC purification of the peptide resulting from the use of 2a to replace the Thr residue, provided mass spectral molecular ions consistent with the desired peptide product [m/z = 1454.5, (M + H) and 1476.5 (M + Na)].
The major fraction obtained by HPLC purification of the peptide resulting from the use of 2a to replace the Thr residue, provided mass spectral molecular ions consistent with the desired peptide product [m/z = 1454.5, (M + H) and 1476.5 (M + Na)].