4‐(4‐Hydroxymethyl)phenoxyacetic Acid
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[1] Jidong Zhang,et al. A colored dendrimer as a new soluble support in organic synthesis. Part 1: Suzuki reaction , 2001 .
[2] M. Bradley,et al. Solid-phase synthesis of oxo(mercaptoacetylglycylglycylglycine)rhenate(V) , 2001 .
[3] J. Kihlberg,et al. Preparation of fluorinated linkers: use of 19F NMR spectroscopy to establish conditions for solid-phase synthesis of pilicide libraries. , 2000, Journal of combinatorial chemistry.
[4] F. Ercole,et al. Improving the performance of an acid‐labile 4‐hydroxymethyl phenoxyacetic acid (HMP) linker on resin and SynPhase™ grafted solid‐supports , 2000, Journal of peptide science : an official publication of the European Peptide Society.
[5] M. Patek,et al. Solid-phase synthesis of substituted guanidines using a novel acid labile linker. , 2000, Journal of combinatorial chemistry.
[6] V. Pillai,et al. Optimization in Peptide Synthetic Conditions of 1,4-Butanediol Dimethacrylate Cross-Linked Polystyrene Resin and its Efficiency in Solid Phase Peptide Synthesis , 2000 .
[7] M. Bradley,et al. Inhibition of the tissue factor/factor VIIa complex — Lead optimisation using combinatorial chemistry , 1999 .
[8] A. W. Czarnik,et al. Polystyrene grafted fluoropolymer microtubes: New supports for solid-phase organic synthesis with useful performance at high temperature , 1999 .
[9] M. Morrissey,et al. Solid-phase synthesis of N-substituted amidinophenoxy pyridines as factor XA inhibitors. , 1998, Bioorganic & medicinal chemistry letters.
[10] M. Bradley,et al. The synthesis of symmetrical spermine conjugates using solid-phase chemistry. , 1998, Bioorganic & medicinal chemistry letters.
[11] S. Teague,et al. Solid-Phase Total Synthesis of Oscillamide Y and Analogues , 1997 .
[12] M. Bradley,et al. A linker for amidines in solid phase synthesis , 1997 .
[13] M. Bradley,et al. C‐Terminally Modified Peptides and Peptide Libraries—Another End to Peptide Synthesis , 1997 .
[14] M. Bradley,et al. A simple multiple release system for combinatorial library and peptide analysis , 1996 .
[15] K. Kaljuste,et al. Solid phase synthesis of 1,2,3,4-tetrahydro-β-carbolines; implications for combinatorial chemistry , 1995 .
[16] W. Chan,et al. Facile synthesis of protected C-terminal peptide segments by Fmoc/But solid-phase procedures on N-Fmoc-9-amino-xanthen-3-yloxymethyl polystyrene resin , 1995 .
[17] D. Harding,et al. Fmoc SPPS using Perloza beaded cellulose. , 2009, International journal of peptide and protein research.
[18] R. Valerio,et al. Multiple peptide synthesis on acid-labile handle derivatized polyethylene supports. , 2009, International journal of peptide and protein research.
[19] T. Gadek,et al. A surprising observation about Mitsunobu reactions in solid phase synthesis , 1994 .
[20] H. Fretz,et al. A General Strategy for the Synthesis of Large Peptides: r1~he Combined Solid-Phase and Solution Approach. , 1993 .
[21] M. Meldal,et al. Small-scale solid-phase O-glycopeptide synthesis of linear and cyclized hexapeptides from blood-clotting factor IX containing O-(α-D-Xyl-1→3-α-D-Xyl-1→3-β-D-Glc)-L-ser , 1993 .
[22] G. Stavropoulos,et al. 2-Chlorotrityl chloride resin. Studies on anchoring of Fmoc-amino acids and peptide cleavage. , 2009, International journal of peptide and protein research.
[23] A. Flörsheimer,et al. Solid-phase synthesis of peptides with the highly acid-sensitive HMPB linker , 1991 .
[24] R. Frank,et al. An efficient method for anchoring fmoc-anino acids to hydroxyl-functionalised solid supports , 1990 .
[25] M. Meldal,et al. Peptide synthesis. Part 12. 3,4-Dihydro-4-oxo-1,2,3-benzotriazin-3-yl esters of fluorenylmethoxycarbonyl amino acids as self-indicating reagents for solid phase peptide synthesis , 1988 .
[26] P. Sieber. An improved method for anchoring of 9-fluorenylmethoxycarbonyl-amino acids to 4-alkoxybenzyl alcohol resins. , 1987 .
[27] R. Sheppard,et al. Use of esters of 2,5-diphenyl-2,3-dihydro-3-oxo-4-hydroxythiophene dioxide in solid phase peptide synthesis. A new procedure for attachment of the first amino acid , 1987 .
[28] H. Rink. Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methylester resin. , 1987 .
[29] P. Sieber. A new acid-labile anchor group for the solid-phase synthesis of C-terminal peptide amides by the Fmoc method. , 1987 .
[30] F. Albericio,et al. Improved approach for anchoring N alpha-9-fluorenylmethyloxycarbonylamino acids as p-alkoxybenzyl esters in solid-phase peptide synthesis. , 2009, International journal of peptide and protein research.
[31] F. Albericio,et al. Application of N,N-dimethylformamide dineopentyl acetal for efficient anchoring of N alpha-9-fluorenylmethyloxycarbonylamino acids as p-alkoxybenzyl esters in solid-phase peptide synthesis. , 2009, International journal of peptide and protein research.
[32] R. Sheppard,et al. Peptide synthesis. Part 3. Comparative solid-phase syntheses of human β-endorphin on polyamide supports using t-butoxycarbonyl and fluorenylmethoxycarbonyl protecting groups , 1983 .
[33] R. Sheppard,et al. Acid-labile resin linkage agents for use in solid phase peptide synthesis. , 2009, International journal of peptide and protein research.
[34] R. Sheppard,et al. Peptide synthesis. Part 2. Procedures for solid-phase synthesis using Nα-fluorenylmethoxycarbonylamino-acids on polyamide supports. Synthesis of substance P and of acyl carrier protein 65–74 decapeptide , 1981 .
[35] R. Sheppard,et al. Racemisation of activated, urethane-protected amino-acids by p-dimethyl-aminopyridine. Significance in solid-phase peptide synthesis , 1981 .
[36] R. Sheppard,et al. Application of polyamide resins to polypeptide synthesis: an improved synthesis of β-endorphin using fluorenylmethoxycarbonylamino-acids , 1978 .
[37] S. S. Wang. p-alkoxybenzyl alcohol resin and p-alkoxybenzyloxycarbonylhydrazide resin for solid phase synthesis of protected peptide fragments. , 1973, Journal of the American Chemical Society.