and Gatfield, I., New, easily removable poly(ethylene glycol) supports for the liquid-phase method of peptide synthesis, J. and Bayer, E., 3-Nitro-4-aminomethylbenzoylderivate von polyethylenglykolen: Eine neue klasse von photosensitiven loslichen polymeren tragern zur synthese von C-terminalen peptidamiden, Tetrahedron Lett., (1979) 3409–3412. and Gurwara, S.K., Removal of C-terminal peptide amides from a 3-nitro-4-aminomethyl-benzoyl amide resin by photolysis, Tetrahedron Lett., (1975) 301–304. and Pillai, V.N.R., Solid-phase synthesis and C-terminal amidation of peptides using a photolabile o-nitrobenz-hydrylamino polystyrene support, Tetrahedron Lett., 36 (1995) 777–780. and Pillai, V.N.R., Solid-phase synthesis of N-methyl- and N-ethylamides of peptides using photolytically detachable ((3-nitro-4-((alkylamino) methyl)benzamido) methyl) polystyrene resin, J.
and Pillai, V.N.R., Selective conversion of chloromethyl and bromomethyl groups to aminomethyl groups in multifunctional crosslinked polystyrenes, Eur. and Pillai, V.N.R., Polymer-supported synthesis of protected peptide segments on a photosensitive o-nitro(α-methyl)bromobenzyl resin, Tetrahedron, 44 (1988) 6661–6664.ĭevaky, K.S.
and Pillai, V.N.R., 2′-Nitrobenzhydryl polystyrene resin: a new photosensitive polymeric support for peptide synthesis, J. Tam, J.P., A gradative deprotection strategy for the solid-phase synthesis of peptide amides using p-(acyloxy)benzhydrylamine resin and the S N2 deprotection method, J. and Stewart, J.M., A p-methylbenzhydryl amine resin for improved solid-phase synthesis of peptide amides, Peptides, 2 (1981) 45–50. Synthesis and use of p-methoxybenz-hydrylamine resin in the solid-phase preparation of peptides, J. and Winkler, D.L., Study of benzhydrylamine-type polymers. and Marshall, G.R., Amide protection and amide supports in solid-phase peptide synthesis, J. Synthesis of substance P and of acyl carrier 65–74 decapeptide, J. Procedures for solid-phase synthesis using N α- fluorenylmethoxycarbonylamino-acids on polyamide supports. and Sheppard, R.C., Peptide synthesis: Part0 2. Manning, M., Synthesis by the Merrifield method of a protected nonapeptide amide with the amino acid sequence of oxytocin, J. and Sheehan, J.T., Active esters and resins in peptide synthesis, Chem. and Moos, W.H., Post-modification of peptoid side chains: cycloaddition of nitrile oxides with alkenes and alkynes on the solid-phase, Tetrahedron Lett., 32 (1994) 5825–5828.īodanszky, M. and Moos, W.H., Discovery of nanomolar ligands for 7-transmembrane G-protein-coupled receptors from a diverse N-(substituted)glycine peptoid library, J. and Schultz, P.G., An unnatural biopolymer, Science, 261 (1993) 1303–1305.įor peptoids see: Zuckermann, R.N., Martin, E.J., Spellmeyer, D.C., Stauber, G.B., Shoemaker, K.R., Kerr, J.M., Figliozzi, G.M., Goff, D.A., Siani, M.A., Simon, R.J., Banville, S.C., Brown, E.G., Wang, L., Richter, L.S. and Santi, D.V., Identification of highest-affinity ligands by affinity selection from equimolar peptide mixtures generated by robotic synthesis, Proc. and Cuervo, J.H., Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery, Nature, 354 (1991) 84–86.įor peptides see: Zuckermann, R.N., Kerr, J.M., Siani, M.A., Banville, S.C.
and Whitehouse, C.M., Electrospray ionization-principles and practice, Mass Spectrom. and Henion, J., The determination of protein oligonucleotide and peptide molecular weights by ion-spray mass spectrometry, J. and Moos, W.H., The generation of molecular diversity, Bioorg. News, (1994) pp20–26.įor recent reviews see: Pavia, M.R., Sawyer, T.K. Chem., 37 (1994) 1233–12–1401.įor recent reviews see: Baum, R.M., Combinatorial approaches provide fresh leads for medicinal chemistry, Chem. and Gordon, E.M., Applications of combinatorial technologies to drug discovery, J. For recent reviews see: Felder, E.D., The challenge of preparing and testing combinatorial compound libraries in the fast lane, at the front end of drug development, Chimia, 48 (1994) 531–541.įor recent reviews see: Gallop, M.A., Barrett, R.W., Dower, W.J., Fodor, S.P.A.
0 kommentar(er)
