-
1
-
-
0344531164
-
-
note
-
2OH; DCC, N,N′-dicyclohexylcarbodiimide; DCU, N,N′-dicyclohexylurea; DIPEA, N,N-diisopropylethylamine; DMAP, (dimethylamino)pyridine; DPDPE, Tyr-cyclo(D-Pen-Gly-Phe-D-Pen)-OH; HBTU, O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate; HATU, O-(7-azabenzotriazol-1-yl]-N,N,N′-tetramethyluronium hexafluorophosphate; HOAt, 1-hydroxy-7-azabenzotriazole; HOBt, 1-hydroxybenzotriazole; IMAC, immobilized metal affinity chromatography; MBHA, p-methylbenzhydrylamine; NMM, N-methylmorpholine; Pen, penicillamine; PyBrOP, bromotrispyrrolidinophosphonium hexafluorophosphate; SP, substance P; SPL, Sybyl programming language; SPPS, solid-phase peptide synthesis; TBAF, tetrabutylammonium fluoride; TBTU, O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate; TFMSA, trifluoromethane-sulfonic acid; TMSI, iodotrimethylsilane; Tos, p-toluenesulfonyl.
-
-
-
-
2
-
-
0023928367
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Amide bond surrogates: Pseudopeptides and macrocycles
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0025336463
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2) and then treating the free amine with (-)-Mosher acid chloride. Analysis of the amide by straight phase HPLC indicated that racemization had occurred during the deprotection with TFA. This finding was also verified by the lack of optical rotation exhibited by the free amine.
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