-
1
-
-
0003564973
-
-
CRC Press, Boca Raton, FL
-
1. Lloyd-Williams, P., Albericio, F. & Giralt, E. (1997) Chemical Approaches to the Synthesis of Peptides and Proteins. CRC Press, Boca Raton, FL.
-
(1997)
Chemical Approaches to the Synthesis of Peptides and Proteins
-
-
Lloyd-Williams, P.1
Albericio, F.2
Giralt, E.3
-
2
-
-
0027373903
-
Convergent solid-phase peptide synthesis
-
2. Lloyd-Williams, P., Albericio, F. & Giralt, E. (1993) Convergent solid-phase peptide synthesis. Tetrahedron 49, 11065-11133.
-
(1993)
Tetrahedron
, vol.49
, pp. 11065-11133
-
-
Lloyd-Williams, P.1
Albericio, F.2
Giralt, E.3
-
3
-
-
0017784004
-
New amino protecting group removable by reduction - Chemistry of dithiasuccinoyl (Dts) function
-
3. Barany, G. & Merrifield, R.B. (1977) New amino protecting group removable by reduction - chemistry of dithiasuccinoyl (Dts) function. J. Am. Chem. Soc. 99, 7363-7365.
-
(1977)
J. Am. Chem. Soc.
, vol.99
, pp. 7363-7365
-
-
Barany, G.1
Merrifield, R.B.2
-
4
-
-
0026727969
-
N-2-(2,4-Dinitrophenyl)ethyloxycarbonylamino acids, new base labile protected derivatives suitable for solid-phase peptide-synthesis
-
4. Acedo, M., Albericio, F. & Eritja, R. (1992) N-2-(2,4-Dinitrophenyl)ethyloxycarbonylamino acids, new base labile protected derivatives suitable for solid-phase peptide-synthesis. Tetrahedron Lett. 33, 4989-4992.
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 4989-4992
-
-
Acedo, M.1
Albericio, F.2
Eritja, R.3
-
5
-
-
84987094735
-
New base-labile amino-protective groups for peptide-synthesis
-
5. Verhart, C.G.J. & Tesser, G.I. (1988) New base-labile amino-protective groups for peptide-synthesis. Recl. Trav. Chim. Pay. B. 107, 621-626.
-
(1988)
Recl. Trav. Chim. Pay. B.
, vol.107
, pp. 621-626
-
-
Verhart, C.G.J.1
Tesser, G.I.2
-
6
-
-
0033546099
-
Amino-protecting groups subject to deblocking under conditions of nucleophilic addition to a Michael acceptor. Structure-reactivity studies and use of the 2-(tert-butylsulfonyl)-2-propenyloxycarbonyl (Bspoc) group
-
6. Carpino, L.A. & Philbin, M. (1999) Amino-protecting groups subject to deblocking under conditions of nucleophilic addition to a Michael acceptor. Structure-reactivity studies and use of the 2-(tert-butylsulfonyl)-2-propenyloxycarbonyl (Bspoc) group. J. Org. Chem. 64, 4315-4323.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 4315-4323
-
-
Carpino, L.A.1
Philbin, M.2
-
7
-
-
0033546356
-
The 1,1-dioxobenzo[b]thiophene-2-ylmethyloxycarbonyl (Bsmoc) amino-protecting group
-
7. Carpino, L.A., Ismail, M., Truran, G.A., Mansour, E.M.E., Iguchi, S., Ionescu, D., El-Faham, A., Riemer, C. & Warrass, R. (1999) The 1,1-dioxobenzo[b]thiophene-2-ylmethyloxycarbonyl (Bsmoc) amino-protecting group. J. Org. Chem. 64, 4324-4338.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 4324-4338
-
-
Carpino, L.A.1
Ismail, M.2
Truran, G.A.3
Mansour, E.M.E.4
Iguchi, S.5
Ionescu, D.6
El-Faham, A.7
Riemer, C.8
Warrass, R.9
-
8
-
-
0028143799
-
2-(4-Nitrophenyl)sulfonylethoxycarbonyl (Nsc) group as a base-labile alpha-amino protection for solid-phase peptide-synthesis
-
8. Samukov, V.V., Sabirov, A.N. & Pozdnyakov, P.I. (1994) 2-(4-Nitrophenyl)sulfonylethoxycarbonyl (Nsc) group as a base-labile alpha-amino protection for solid-phase peptide-synthesis. Tetrahedron Lett. 35, 7821-7824.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 7821-7824
-
-
Samukov, V.V.1
Sabirov, A.N.2
Pozdnyakov, P.I.3
-
11
-
-
1542755747
-
Correlation of coupling rates with physicochemical properties of resin-bound peptides in solid phase synthesis
-
Peptides: Structure and Function, (Hruby, V.J. & Rich, D.H., eds). Pierce Chemical Co, Rockford, IL
-
11. Live, D.H. & Kent, S.B.H. (1984) Correlation of coupling rates with physicochemical properties of resin-bound peptides in solid phase synthesis. In Peptides: Structure and Function, Proceedings of the Eighth American Peptide Symposium (Hruby, V.J. & Rich, D.H., eds). Pierce Chemical Co, Rockford, IL, pp. 65-68.
-
(1984)
Proceedings of the Eighth American Peptide Symposium
, pp. 65-68
-
-
Live, D.H.1
Kent, S.B.H.2
-
12
-
-
0029572443
-
Coupling difficulty associated with interchain clustering and phase-transition in solid-phase peptide-synthesis
-
12. Tam, J.P. & Lu, Y.A. (1995) Coupling difficulty associated with interchain clustering and phase-transition in solid-phase peptide-synthesis. J. Am. Chem. Soc. 117, 12058-12063.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 12058-12063
-
-
Tam, J.P.1
Lu, Y.A.2
-
13
-
-
85069104505
-
Automatic solid-phase peptide synthesis
-
(Kates, S.A. & Alberieio, F., eds). Marcel Dekker, New York
-
13. Daniels, S. (2000) Automatic solid-phase peptide synthesis. In Solid-Phase Peptide Synthesis, a Practical Guide (Kates, S.A. & Alberieio, F., eds). Marcel Dekker, New York.
-
(2000)
Solid-phase Peptide Synthesis, A Practical Guide
-
-
Daniels, S.1
-
14
-
-
0026151057
-
γ-deprotecting reagent for the fluorenylmethoxycarbonyl group in continuous flow solid-phase peptide synthesis
-
γ-deprotecting reagent for the fluorenylmethoxycarbonyl group in continuous flow solid-phase peptide synthesis. Peptide Res. 4, 194-199.
-
(1991)
Peptide Res.
, vol.4
, pp. 194-199
-
-
Wade, J.D.1
Bedford, J.2
Sheppard, R.C.3
Tregear, G.W.4
-
15
-
-
0030152676
-
Optimized preparation of deca (I-alanyl) -L-valinamide by 9-fluorenylmethyloxycarbonyl (Fmoc) solid-phase synthesis on polyethylene glycolpolystyrene (PEG-PS) graft supports, with 1,8-diazobicyclo[5.4.0]-undec-7-ene (DBU) deprotection
-
15. Kates, S.A., Solé, N.A., Beyermann, M., Barany, G. & Albericio, F. (1996) Optimized preparation of deca (I-alanyl) -L-valinamide by 9-fluorenylmethyloxycarbonyl (Fmoc) solid-phase synthesis on polyethylene glycolpolystyrene (PEG-PS) graft supports, with 1,8-diazobicyclo[5.4.0]-undec-7-ene (DBU) deprotection. Peptide Res. 9, 106-113.
-
(1996)
Peptide Res.
, vol.9
, pp. 106-113
-
-
Kates, S.A.1
Solé, N.A.2
Beyermann, M.3
Barany, G.4
Albericio, F.5
-
16
-
-
0008318633
-
A robotic workstation for automated multiple peptide synthesis
-
(Epton, R., ed.). SPCCC Ltd, Birmingham, UK
-
16. Gausepohl, H., Kraft, M., Boulin, C. & Frank, R.W. (1990) A robotic workstation for automated multiple peptide synthesis. In Innovation and Perspectives in Solid Phase Synthesis, Peptides, Polypeptides and Oligonucleotides (Epton, R., ed.). SPCCC Ltd, Birmingham, UK, pp. 487-490.
-
(1990)
Innovation and Perspectives in Solid Phase Synthesis, Peptides, Polypeptides and Oligonucleotides
, pp. 487-490
-
-
Gausepohl, H.1
Kraft, M.2
Boulin, C.3
Frank, R.W.4
-
17
-
-
0000748775
-
Solvation of the polymer matrix. Source of truncated and deletion sequences in solid phase synthesis
-
17. Hancock, W.S., Prescott, D.J., Vagelos, P.R. & Marshall, G.R. (1973) Solvation of the polymer matrix. Source of truncated and deletion sequences in solid phase synthesis. J. Org. Chem. 38, 774-781.
-
(1973)
J. Org. Chem.
, vol.38
, pp. 774-781
-
-
Hancock, W.S.1
Prescott, D.J.2
Vagelos, P.R.3
Marshall, G.R.4
-
18
-
-
0001065043
-
'Magic mixture', a powerful solvent system for solid-phase synthesis of 'difficult sequences'
-
(Epton, R., ed.). Mayflower Worlwide Ltd, Birmingham, UK
-
18. Zhang, L., Goldammer, C., Henkel, B., Zühl, F., Panhaus, G., Jung, G. & Bayer, E. (1994) 'Magic mixture', a powerful solvent system for solid-phase synthesis of 'difficult sequences'. In Innovation and Perspectives in Solid Phase Synthesis, Peptides, Proteins and Nucleic Acids (Epton, R., ed.). Mayflower Worlwide Ltd, Birmingham, UK, pp. 711-716.
-
(1994)
Innovation and Perspectives in Solid Phase Synthesis, Peptides, Proteins and Nucleic Acids
, pp. 711-716
-
-
Zhang, L.1
Goldammer, C.2
Henkel, B.3
Zühl, F.4
Panhaus, G.5
Jung, G.6
Bayer, E.7
-
19
-
-
0023212002
-
Subtyping of european foot-and-mouth disease virus strains by nucleotide sequence setermination
-
19. Beck, E. & Strohmaier, K. (1987) Subtyping of European foot-and-mouth disease virus strains by nucleotide sequence setermination. J. Virol. 61, 1621-1629.
-
(1987)
J. Virol.
, vol.61
, pp. 1621-1629
-
-
Beck, E.1
Strohmaier, K.2
-
20
-
-
0000875125
-
Sequence dependence of aspartimide formation during 9-fluorenylmethoxyearbonyl solid-phase peptide synthesis
-
20. Lauer, J.L., Fields, C.G. & Fields, G.B. (1994) Sequence dependence of aspartimide formation during 9-fluorenylmethoxyearbonyl solid-phase peptide synthesis. Lett. Peptide Sci. 1, 197-205.
-
(1994)
Lett. Peptide Sci.
, vol.1
, pp. 197-205
-
-
Lauer, J.L.1
Fields, C.G.2
Fields, G.B.3
-
22
-
-
0008315321
-
Use of polar picolyl protecting groups in peptide synthesis
-
22. Rizo, J., Albericio, F., Romero, G., Garcia-Echeverria, C., Claret, J., Muller, C., Giralt, E. & Pedroso, E. (1988) Use of polar picolyl protecting groups in peptide synthesis. J. Org. Chem. 53, 5836-5839.
-
(1988)
J. Org. Chem.
, vol.53
, pp. 5836-5839
-
-
Rizo, J.1
Albericio, F.2
Romero, G.3
Garcia-Echeverria, C.4
Claret, J.5
Muller, C.6
Giralt, E.7
Pedroso, E.8
-
23
-
-
0001587747
-
Racemization in peptide synthesis
-
(Gross, E. & Meienhofer, J., eds). Academic Press, New York
-
23. Kemp, D.S. (1989) Racemization in peptide synthesis. In The Peptides, Analysis, Synthesis, Biology, Vol. 2 (Gross, E. & Meienhofer, J., eds). Academic Press, New York, pp. 315-383.
-
(1989)
The Peptides, Analysis, Synthesis, Biology
, vol.2
, pp. 315-383
-
-
Kemp, D.S.1
-
24
-
-
0002801677
-
Coupling methods: Solid-phase formation of amide and ester bonds
-
(Kates, S.A. & Alhericio, F., eds). Marcel Dekker, New York
-
24. Albericio, F. & Kates, S.A. (2000) Coupling methods: solid-phase formation of amide and ester bonds. In Solid-Phase Peptide Synthesis, a Practical Guide (Kates, S.A. & Alhericio, F., eds). Marcel Dekker, New York.
-
(2000)
Solid-phase Peptide Synthesis, A Practical Guide
-
-
Albericio, F.1
Kates, S.A.2
-
25
-
-
0002714866
-
The racemization of histidine in peptide synthesis: Further studies
-
Peptides 1994. (Maia, H.L.S., ed.). Escom Science, Leiden, The Netherlands
-
25. Harding, S.J., Heslop, I., Jones, J.H. & Wood, M.E. (1995) The racemization of histidine in peptide synthesis: further studies. In Peptides 1994. Proceedings of the Twenty-Third European Peptide Symposium (Maia, H.L.S., ed.). Escom Science, Leiden, The Netherlands, pp. 189-190.
-
(1995)
Proceedings of the Twenty-third European Peptide Symposium
, pp. 189-190
-
-
Harding, S.J.1
Heslop, I.2
Jones, J.H.3
Wood, M.E.4
-
26
-
-
0028004425
-
Redox-active bis-cysteinyl peptides. 1. Synthesis of cyclic cystinyl peptides by conventional methods in solution and on solid supports
-
26. Musiol, H.J., Siedler, F., Quarzago, D. & Moroder, L. (1994) Redox-active bis-cysteinyl peptides. 1. Synthesis of cyclic cystinyl peptides by conventional methods in solution and on solid supports. Biopolymers 34, 1553-1562.
-
(1994)
Biopolymers
, vol.34
, pp. 1553-1562
-
-
Musiol, H.J.1
Siedler, F.2
Quarzago, D.3
Moroder, L.4
-
27
-
-
0000277428
-
Occurrence and minimization of cysteine racemization during stepwise solid-phase peptide synthesis
-
27. Han, Y.X., Albericio, F. & Barany, G. (1997) Occurrence and minimization of cysteine racemization during stepwise solid-phase peptide synthesis. J. Org. Chem. 62, 4307-4312.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 4307-4312
-
-
Han, Y.X.1
Albericio, F.2
Barany, G.3
-
28
-
-
0032512076
-
Racemization studies of Fmoc-Ser(tBu)-OH during stepwise continuous-flow solid-phase peptide synthesis
-
28. Di Fenza, A., Tancredi, M., Galoppini, C. & Rovero, P. (1998) Racemization studies of Fmoc-Ser(tBu)-OH during stepwise continuous-flow solid-phase peptide synthesis. Tetrahedron Lett. 39, 8529-8532.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 8529-8532
-
-
Di Fenza, A.1
Tancredi, M.2
Galoppini, C.3
Rovero, P.4
-
29
-
-
0033612107
-
The diisopropylcarbodiimide/1-hydroxy-7-azabenzotriazole system: Segment coupling and stepwise peptide assembly
-
29. Carpino, L.A. & El-Faham, A. (1999) The diisopropylcarbodiimide/1-hydroxy-7-azabenzotriazole system: segment coupling and stepwise peptide assembly. Tetrahedron 55, 6813-6830.
-
(1999)
Tetrahedron
, vol.55
, pp. 6813-6830
-
-
Carpino, L.A.1
El-Faham, A.2
-
30
-
-
33845279240
-
Methodological implications of simultaneous solid-phase peptide-synthesis. 1. Comparison of different coupling procedures
-
30. Hudson, D. (1988) Methodological implications of simultaneous solid-phase peptide-synthesis. 1. Comparison of different coupling procedures. J. Org. Chem. 53, 617-614.
-
(1988)
J. Org. Chem.
, vol.53
, pp. 617-1614
-
-
Hudson, D.1
|