SPPS is a widely used method for peptide synthesis. Attach the first amino acid (usually the core of the dendrimer) to a solid support, and then add subsequent amino acids one by one, building the dendrimer layer by layer. Each amino acid should be activated for coupling with a suitable reagent like DIC/HOBt.
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(S)-tert-butyl 3-((1R,3R)-3-acetyl-2,2-dimethylcyclobutyl)-4-(4-(benzyloxycarbonylamino)butanamido)butanoate
Glycine, N-[N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)-L-seryl]-, methyl ester
2-Formylamino-N-(N'-phenyl-hydrazinocarbonylmethyl)-acetamide
Nα-dinicotinoylbis(L-leucyl-L-phenylalanine)
C23H32N2O5
(R)-3-{(S)-2-[(S)-6-Benzyloxycarbonylamino-2-(2-tert-butoxycarbonylamino-acetylamino)-hexanoylamino]-3-methyl-butyrylamino}-tetradecanoic acid
Fmoc-Cys(STmp)-OH
Glycine, N-[N-[(phenylmethoxy)carbonyl]thioglycyl]-, methyl ester
1H-Imidazole-2-carboxylicacid,4-amino-1-methyl-(9CI)
Mtz-Ile-Ser(Mtb)-Asp-Arg-Asp-Tyr(SO3H)-Met-Gly-Trp-Met-Asp-Phe-NH2
N-[(1S-(1α,2α,1'α))-2-(2'-azido)ethan-1'-ol-cyclopropan-1-oyl]-L-phenylalanine-L-leucine
C27H39N5O8S
phenyl 6-O-tert-butyldimethylsilyl-2,3,4-tri-O-4-methoxybenzyl-1-thio-α-D-mannopyranoside
(S)-2-((tert-butoxycarbonyl)amino)-5-oxo-5-phenylpentanoic acid
L-Serine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl]-, hydrazide
N-Boc-O-(4-hydroxyphenacyl)-Ala-Ala
MBzl-S-CH2-CH2-CO-Asp-Thr-Ala-NHNH2
L-Methioninamide, L-phenylalanyl-L-phenylalanylglycyl-L-leucyl-, monohydrochloride
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-4-fluoro-N-methyl-3-nitro-
Boc-Ser(cyclohexen-3-yl)-OH
2-hydroxy-5-(6-iodo-2-methyl-4-oxo-3,4-dihydro-3-quinazolinyl)benzoyltyrosine
(2S,5S,11bR,1'S)-2-[(Nα-(tert-butoxycarbonyl)-L-tryptophyl)amino]-5-[(1'-methoxycarbonyl-2'-phenyl)ethyl]carbamoyl-3-oxo-2,3,5,6,11,11b-hexahydro-1H-indolizino[8,7-b]indole
α-(tert-butyloxycarbonylamino)-Nα-(benzyloxycarbonyl)glycine methyl ester
benzyl methyl aminomalonate hydrochloride
2-Methylalanine
methyl (L-2-(benzyloxy)-4-methylpentanoyl)-L-alaninate
