-
2
-
-
0000664191
-
Conformational studies of poly(-oxyethylene)-bound peptides and protein sequences
-
Pillai V, Mutter M. Conformational studies of poly(-oxyethylene)-bound peptides and protein sequences. Acc. Chem. Res. 1981; 14: 122-130.
-
(1981)
Acc. Chem. Res.
, vol.14
, pp. 122-130
-
-
Pillai, V.1
Mutter, M.2
-
3
-
-
0025130364
-
An improved solid-phase synthesis of a difficult-sequence peptide using hexafluoro-2-propanol
-
Milton SCF, Milton RCD. An improved solid-phase synthesis of a difficult-sequence peptide using hexafluoro-2-propanol. Int. J. Peptide Protein Res. 1990; 36: 193-196.
-
(1990)
Int. J. Peptide Protein Res.
, vol.36
, pp. 193-196
-
-
Milton, S.C.F.1
Milton, R.C.D.2
-
4
-
-
2142738799
-
Increased coupling efficiency in solid-phase peptide synthesis using elevated temperature
-
Rivier JE, Marshall GR (eds). ESCOM Lerden
-
Lloyd DH, Petrie GM, Noble RL, Tam JP. Increased coupling efficiency in solid-phase peptide synthesis using elevated temperature. In Peptides: Chemistry Structure and Biology, Rivier JE, Marshall GR (eds). ESCOM Lerden, 1990, pp. 909-910.
-
(1990)
Peptides: Chemistry Structure and Biology
, pp. 909-910
-
-
Lloyd, D.H.1
Petrie, G.M.2
Noble, R.L.3
Tam, J.P.4
-
5
-
-
0026439294
-
Effects of resin swelling and substitution on solid phase synthesis
-
Pugh KC, York EH, Stewart JM. Effects of resin swelling and substitution on solid phase synthesis. Int. J. Peptide Protein Res. 1992; 40: 208-213.
-
(1992)
Int. J. Peptide Protein Res.
, vol.40
, pp. 208-213
-
-
Pugh, K.C.1
York, E.H.2
Stewart, J.M.3
-
6
-
-
0346575816
-
Solubilizing protecting groups in peptide synthesis. Effect of side-chain-attached poly(ethyleneglycol) derivatives upon β-sheet formation of model peptides
-
Mutter M, Oppliger H, Zier A. Solubilizing protecting groups in peptide synthesis. Effect of side-chain-attached poly(ethyleneglycol) derivatives upon β-sheet formation of model peptides. Mokromol. Chem. Rapid Commun. 1992; 13: 151-157.
-
(1992)
Mokromol. Chem. Rapid Commun.
, vol.13
, pp. 151-157
-
-
Mutter, M.1
Oppliger, H.2
Zier, A.3
-
7
-
-
0028233684
-
Some 'difficult sequences' made easy
-
Hyde C, Johnson T, Owen D, Quibell M, Sheppard RC. Some 'difficult sequences' made easy. Int. J. Peptide Protein Res. 1994; 43: 431-440.
-
(1994)
Int. J. Peptide Protein Res.
, vol.43
, pp. 431-440
-
-
Hyde, C.1
Johnson, T.2
Owen, D.3
Quibell, M.4
Sheppard, R.C.5
-
8
-
-
0029171221
-
N,O-bisFmoc derivatives of N-(2-hydroxy-4-methoxybenzyl)-amino acids: Useful intermediates in peptide synthesis
-
Johnson T, Quibell M, Sheppard RC. N,O-bisFmoc derivatives of N-(2-hydroxy-4-methoxybenzyl)-amino acids: useful intermediates in peptide synthesis. J. Peptide Sci. 1995; 1: 11-25.
-
(1995)
J. Peptide Sci.
, vol.1
, pp. 11-25
-
-
Johnson, T.1
Quibell, M.2
Sheppard, R.C.3
-
9
-
-
0002543138
-
Backbone protection: Synthesis of difficult sequences using N-α-Tmob-protected amino acid derivatives
-
Kaumaya FTP, Hodges RS (eds), UK: Mayflower Scientific
-
Clausen N, Goldammer C, Jauch K, Bayer E. Backbone protection: synthesis of difficult sequences using N-α-Tmob-protected amino acid derivatives. In Peptides. Chemistry, Structure and Biology, Kaumaya FTP, Hodges RS (eds), UK: Mayflower Scientific, 1996; 71-72.
-
(1996)
Peptides. Chemistry, Structure and Biology
, pp. 71-72
-
-
Clausen, N.1
Goldammer, C.2
Jauch, K.3
Bayer, E.4
-
10
-
-
0028994059
-
Pseudo-Prolines (ΨPro) for accessing 'inaccessible' peptides
-
Mutter M, Nefzi A, Sato T, Sun X, Wahl T, Wuhr T. Pseudo-Prolines (ΨPro) for accessing 'inaccessible' peptides. Peptide Res. 1995; 8: 145-153.
-
(1995)
Peptide Res.
, vol.8
, pp. 145-153
-
-
Mutter, M.1
Nefzi, A.2
Sato, T.3
Sun, X.4
Wahl, T.5
Wuhr, T.6
-
11
-
-
0029952823
-
Pseudo-prolines as a solubilizing, structure-disrupting protection technique in peptide synthesis
-
Woehr T, Wahl F, Nefzi A, Rohwedder B, Sato T, Sun X, Mutter M. Pseudo-prolines as a solubilizing, structure-disrupting protection technique in peptide synthesis. J. Am. Chem. Soc. 1996; 118: 9218-9227.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 9218-9227
-
-
Woehr, T.1
Wahl, F.2
Nefzi, A.3
Rohwedder, B.4
Sato, T.5
Sun, X.6
Mutter, M.7
-
12
-
-
0031028387
-
Pseudo-prolines as a molecular hinge: Reversible induction of cis amide bonds into peptide backbones
-
Dumy P, Kellar M, Ryan DE, Rohwedder B, Woehr T, Mutter M. Pseudo-prolines as a molecular hinge: reversible induction of cis amide bonds into peptide backbones. J. Am. Chem. Soc. 1997; 119: 918-925.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 918-925
-
-
Dumy, P.1
Kellar, M.2
Ryan, D.E.3
Rohwedder, B.4
Woehr, T.5
Mutter, M.6
-
13
-
-
0026150303
-
A synthetic peptide of influenza virus hemagglutinin as a model antigen and immunogen
-
Jackson DC, Brown LE. A synthetic peptide of influenza virus hemagglutinin as a model antigen and immunogen. Peptide Res. 1991; 4: 114-124.
-
(1991)
Peptide Res.
, vol.4
, pp. 114-124
-
-
Jackson, D.C.1
Brown, L.E.2
-
14
-
-
0027964755
-
Multiple peptide synthesis on acid-labile handle derivatized polyethylene supports
-
Valerio RM, Bray AM, Maeji NJ. Multiple peptide synthesis on acid-labile handle derivatized polyethylene supports. Int. J. Peptide Protein Res. 1994; 44: 158-165.
-
(1994)
Int. J. Peptide Protein Res.
, vol.44
, pp. 158-165
-
-
Valerio, R.M.1
Bray, A.M.2
Maeji, N.J.3
-
15
-
-
0025449880
-
Color-monitored solid-phase multiple peptide synthesis under low-pressure continuous-flow conditions
-
Krchnak V, Vagner J. Color-monitored solid-phase multiple peptide synthesis under low-pressure continuous-flow conditions. Peptide Res. 1990; 3: 182-193.
-
(1990)
Peptide Res.
, vol.3
, pp. 182-193
-
-
Krchnak, V.1
Vagner, J.2
-
16
-
-
0030031445
-
High-throughput purity estimation and characterization of synthetic peptides by electrospray mass spectrometry
-
Smart SS, Mason TJ, Bennell PS, Maeji NJ, Geysen HM. High-throughput purity estimation and characterization of synthetic peptides by electrospray mass spectrometry. Int. J. Peptide Protein Res. 1996; 47: 47-55.
-
(1996)
Int. J. Peptide Protein Res.
, vol.47
, pp. 47-55
-
-
Smart, S.S.1
Mason, T.J.2
Bennell, P.S.3
Maeji, N.J.4
Geysen, H.M.5
-
17
-
-
37049075014
-
Improved preparation of β-amyloid(1-43): Structural insight leading to optimized positioning of N-(2-hydroxy-4-methoxybenzyl) (Hmb) backbone amide protection
-
Quibell M, Turnell WG, Johnson T. Improved preparation of β-amyloid(1-43): structural insight leading to optimized positioning of N-(2-hydroxy-4-methoxybenzyl) (Hmb) backbone amide protection. J. Chem. Soc. Perkin Trans. 1 1995; 2019-2024.
-
(1995)
J. Chem. Soc. Perkin Trans. 1
, pp. 2019-2024
-
-
Quibell, M.1
Turnell, W.G.2
Johnson, T.3
-
18
-
-
37049087217
-
A reversible protecting group for the amide bond in peptides. Use in the synthesis of 'difficult sequences'
-
Johnson T, Quibell M, Owen D, Sheppard RC. A reversible protecting group for the amide bond in peptides. Use in the synthesis of 'difficult sequences'. J. Chem. Soc. Chem Commun. 1993; 4: 369-372.
-
(1993)
J. Chem. Soc. Chem Commun.
, vol.4
, pp. 369-372
-
-
Johnson, T.1
Quibell, M.2
Owen, D.3
Sheppard, R.C.4
-
19
-
-
0028834758
-
Synthesis of the 3-repeat region of human tau-2 by the solid phase assembly of backbone amide-protected segments
-
Quibell M, Packman LC, Johnson T. Synthesis of the 3-repeat region of human tau-2 by the solid phase assembly of backbone amide-protected segments. J. Am. Chem. Soc. 1995; 117: 11656-11668.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 11656-11668
-
-
Quibell, M.1
Packman, L.C.2
Johnson, T.3
-
20
-
-
0030974745
-
Use of Fmoc-N-(2-hydroxy-4-methoxybenzyl)amino acids in peptide synthesis
-
Zeng W, Regamey P-O, Rose K, Wang Y, Bayer E. Use of Fmoc-N-(2-hydroxy-4-methoxybenzyl)amino acids in peptide synthesis. Int. J. Peptide Protein Res. 1997; 49: 273-279.
-
(1997)
Int. J. Peptide Protein Res.
, vol.49
, pp. 273-279
-
-
Zeng, W.1
Regamey, P.-O.2
Rose, K.3
Wang, Y.4
Bayer, E.5
-
21
-
-
4244061816
-
Suppression of piperidine-mediated side product formation for Asp(OBut)-containing peptides by the use of N-(2-hydroxy-4-methoxybenzyl) (Hmb) backbone amide protection
-
Quibell M, Owen D, Packman LC, Johnson T. Suppression of piperidine-mediated side product formation for Asp(OBut)-containing peptides by the use of N-(2-hydroxy-4-methoxybenzyl) (Hmb) backbone amide protection. J. Chem. Soc. Chem. Commun. 1994; 2343-2344.
-
(1994)
J. Chem. Soc. Chem. Commun.
, pp. 2343-2344
-
-
Quibell, M.1
Owen, D.2
Packman, L.C.3
Johnson, T.4
-
22
-
-
1542576118
-
On-resin solid-phase synthesis of asparagine N-linked glycopeptides: Use of N-(2-acetoxy-4-methoxybenzyl) (AcHmb) aspartyl amide-bond protection to prevent unwanted aspartimide formation
-
Offer J, Quibell M, Johnson T. On-resin solid-phase synthesis of asparagine N-linked glycopeptides: use of N-(2-acetoxy-4-methoxybenzyl) (AcHmb) aspartyl amide-bond protection to prevent unwanted aspartimide formation. J. Chem. Soc. Perkin Trans. 1 1996; 175-182.
-
(1996)
J. Chem. Soc. Perkin Trans. 1
, pp. 175-182
-
-
Offer, J.1
Quibell, M.2
Johnson, T.3
-
23
-
-
0001251787
-
Orthogonal solid-phase synthesis of N-glycopeptides using backbone protection to eliminate aspartimide formation
-
Urge L, Otvos L. Orthogonal solid-phase synthesis of N-glycopeptides using backbone protection to eliminate aspartimide formation. Lett. Pept. Sci 1995; 1: 207-212.
-
(1995)
Lett. Pept. Sci
, vol.1
, pp. 207-212
-
-
Urge, L.1
Otvos, L.2
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