-
1
-
-
0033397158
-
Polypeptide synthesis by the thioester method
-
Aimoto S. Polypeptide synthesis by the thioester method. Biopolymers (Peptide Sci.) 1999; 51: 247-265.
-
(1999)
Biopolymers (Peptide Sci.)
, vol.51
, pp. 247-265
-
-
Aimoto, S.1
-
2
-
-
0033791223
-
Synthesis of native protein by chemical ligation
-
Dawson PE, Kent SBH. Synthesis of native protein by chemical ligation. Annu. Rev. Biochem. 2000; 69: 923-960.
-
(2000)
Annu. Rev. Biochem.
, vol.69
, pp. 923-960
-
-
Dawson, P.E.1
Kent, S.B.H.2
-
5
-
-
33751034904
-
Emerging methods in amide- and peptide-bond formation
-
Bode JW. Emerging methods in amide- and peptide-bond formation. Curr. Opin. Drug Discov. Devel. 2006; 9: 765-775.
-
(2006)
Curr. Opin. Drug Discov. Devel.
, vol.9
, pp. 765-775
-
-
Bode, J.W.1
-
6
-
-
77958450463
-
Semisynthesis of a protein with cholesterol at the C-terminal, targeted to the cell membrane of live cells
-
Teruya K, Nishizawa K, Doh-ura K. Semisynthesis of a protein with cholesterol at the C-terminal, targeted to the cell membrane of live cells. Protein J. 2010; 29: 493-500.
-
(2010)
Protein J.
, vol.29
, pp. 493-500
-
-
Teruya, K.1
Nishizawa, K.2
Doh-ura, K.3
-
7
-
-
0028940110
-
Synthesis of large peptides in solution
-
Sakakibara S. Synthesis of large peptides in solution. Biopolymers (Peptide Sci.) 1995; 37: 17-28.
-
(1995)
Biopolymers (Peptide Sci.)
, vol.37
, pp. 17-28
-
-
Sakakibara, S.1
-
8
-
-
0037127488
-
Total synthesis of [L40I, C90A, C109A]-human T-cell leukemia virus type-1 protease
-
Teruya K, Kawakami T, Akaji K, Aimoto S. Total synthesis of [L40I, C90A, C109A]-human T-cell leukemia virus type-1 protease. Tetrahedron Lett. 2002; 43: 1487-1490.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 1487-1490
-
-
Teruya, K.1
Kawakami, T.2
Akaji, K.3
Aimoto, S.4
-
9
-
-
0033525874
-
Stabilization from autoproteolysis and kinetic characterization of the human T-cell leukemia virus type 1 proteinase
-
Louis JM, Oroszlan S, Tozser J. Stabilization from autoproteolysis and kinetic characterization of the human T-cell leukemia virus type 1 proteinase. J. Biol. Chem. 1999; 274: 6660-6666.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 6660-6666
-
-
Louis, J.M.1
Oroszlan, S.2
Tozser, J.3
-
10
-
-
0029891170
-
Convergent synthesis of (-)-mirabazole C using a chloroimidazolidium coupling reagent, CIP
-
Akaji K, Kuriyama N, Kiso Y. Convergent synthesis of (-)-mirabazole C using a chloroimidazolidium coupling reagent, CIP. J. Org. Chem. 1996; 61: 3350-3357.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 3350-3357
-
-
Akaji, K.1
Kuriyama, N.2
Kiso, Y.3
-
11
-
-
0025103048
-
A cleavage method which minimizes side reactions following Fmoc solid phase peptide synthesis
-
King DS, Fields CG, Fields GB. A cleavage method which minimizes side reactions following Fmoc solid phase peptide synthesis. Int. J. peptide Protein Res. 1990; 36: 255-266.
-
(1990)
Int. J. peptide Protein Res.
, vol.36
, pp. 255-266
-
-
King, D.S.1
Fields, C.G.2
Fields, G.B.3
-
12
-
-
0000189651
-
Density-functional thermochemistry. III. The role of exact exchange
-
Becke AD. Density-functional thermochemistry. III. The role of exact exchange. J. Chem. Phys. 1993; 98: 5648-5652.
-
(1993)
J. Chem. Phys.
, vol.98
, pp. 5648-5652
-
-
Becke, A.D.1
-
13
-
-
0141509423
-
Contracted Gaussian basis sets for molecular calculations. I. Second row atoms, Z=11-18
-
McLean AD, Chandler GS. Contracted Gaussian basis sets for molecular calculations. I. Second row atoms, Z=11-18. J. Chem. Phys. 1980; 72: 5639-5648.
-
(1980)
J. Chem. Phys.
, vol.72
, pp. 5639-5648
-
-
McLean, A.D.1
Chandler, G.S.2
-
14
-
-
26844534384
-
Self-consistent orbital methods. XX. A basis set for correlated wave functions
-
Krishnan R, Binkley JS, Seeger R, Pople JA. Self-consistent orbital methods. XX. A basis set for correlated wave functions. J. Chem. Phys. 1980; 72: 650-654.
-
(1980)
J. Chem. Phys.
, vol.72
, pp. 650-654
-
-
Krishnan, R.1
Binkley, J.S.2
Seeger, R.3
Pople, J.A.4
-
17
-
-
0014961425
-
Microanalysis by successive isotopic dilution. A new assay for racemic content
-
Kemp DS, Wang SW, Busby G III, Hugel G. Microanalysis by successive isotopic dilution. A new assay for racemic content. J. Am. Chem. Soc. 1970; 92: 1043-1055.
-
(1970)
J. Am. Chem. Soc.
, vol.92
, pp. 1043-1055
-
-
Kemp, D.S.1
Wang, S.W.2
Busby III, G.3
Hugel, G.4
-
18
-
-
0000789462
-
Peptide synthesis via active esters. IV. Racemization and ring-opening reactions of optically active oxazolones
-
Goodman M, Levine L. Peptide synthesis via active esters. IV. Racemization and ring-opening reactions of optically active oxazolones. J. Am. Chem. Soc. 1964; 86: 2918-2922.
-
(1964)
J. Am. Chem. Soc.
, vol.86
, pp. 2918-2922
-
-
Goodman, M.1
Levine, L.2
-
19
-
-
0019531428
-
Studies on racemization during coupling using a series of model tripeptides involving activated residues with unfunctionalized side chains
-
Benoiton NL, Kuroda K. Studies on racemization during coupling using a series of model tripeptides involving activated residues with unfunctionalized side chains. Int. J. Peptide Protein Res. 1981; 17: 197-204.
-
(1981)
Int. J. Peptide Protein Res.
, vol.17
, pp. 197-204
-
-
Benoiton, N.L.1
Kuroda, K.2
-
20
-
-
0001894339
-
Quantitative description of epimerization pathways using the carbodiimide method in the synthesis of peptides
-
Griehl C, Kolbe A, Merkel S. Quantitative description of epimerization pathways using the carbodiimide method in the synthesis of peptides. J. Chem. Soc., Perkin Trans. 2 1996; 2525-2529.
-
(1996)
J. Chem. Soc., Perkin Trans. 2
, pp. 2525-2529
-
-
Griehl, C.1
Kolbe, A.2
Merkel, S.3
-
21
-
-
79551670677
-
9-Fluorenylmethoxycarbonyl-based solid-phase synthesis of peptide α-thioesters
-
Mende F, Seitz O. 9-Fluorenylmethoxycarbonyl-based solid-phase synthesis of peptide α-thioesters. Angew. Chem. Int. Ed Engl. 2011; 50: 1232-1240.
-
(2011)
Angew. Chem. Int. Ed Engl.
, vol.50
, pp. 1232-1240
-
-
Mende, F.1
Seitz, O.2
-
22
-
-
79960036110
-
Base-catalyzed racemization of amino acid derivatives
-
D'Arrigo P, Arosio D, Cerioli L, Moscatelli D, Servi S, Viani F, Tessaro D. Base-catalyzed racemization of amino acid derivatives. Tetrahedron Asymmetry 2011; 22: 851-856.
-
(2011)
Tetrahedron Asymmetry
, vol.22
, pp. 851-856
-
-
D'Arrigo, P.1
Arosio, D.2
Cerioli, L.3
Moscatelli, D.4
Servi, S.5
Viani, F.6
Tessaro, D.7
-
23
-
-
0037123657
-
Racemization of (S)-profen thioesters by strong neutral bases in nonpolar organic solvents: implication for ion-pair kinetic basicity
-
Chen CY, Chang YS, Lin SA, Wen HI, Cheng YC, Tsai SW. Racemization of (S)-profen thioesters by strong neutral bases in nonpolar organic solvents: implication for ion-pair kinetic basicity. J. Org. Chem. 2002; 67: 3323-3326.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 3323-3326
-
-
Chen, C.Y.1
Chang, Y.S.2
Lin, S.A.3
Wen, H.I.4
Cheng, Y.C.5
Tsai, S.W.6
-
24
-
-
79960244208
-
Evolution of amide bond formation
-
Joullié MM, Lassen KM. Evolution of amide bond formation. Arkivoc 2010; 8: 189-250.
-
(2010)
Arkivoc
, vol.8
, pp. 189-250
-
-
Joullié, M.M.1
Lassen, K.M.2
-
26
-
-
0001360037
-
Synthesis of cysteine-containing polypeptide using a peptide thioester containing a Cys(Acm) residue
-
Kawakami T, Kogure S, Aimoto S. Synthesis of cysteine-containing polypeptide using a peptide thioester containing a Cys(Acm) residue. Bull. Chem. Soc. Jpn. 1996; 69: 3331-3338.
-
(1996)
Bull. Chem. Soc. Jpn.
, vol.69
, pp. 3331-3338
-
-
Kawakami, T.1
Kogure, S.2
Aimoto, S.3
-
27
-
-
0024500435
-
Development of a facile method for polypeptide synthesis. Synthesis of bovine pancreatic trypsin inhibitor (BPTI)
-
Aimoto S, Mizoguchi N, Hojo H, Yoshimura S. Development of a facile method for polypeptide synthesis. Synthesis of bovine pancreatic trypsin inhibitor (BPTI). Bull. Chem. Soc. Jpn. 1989; 62: 524-531.
-
(1989)
Bull. Chem. Soc. Jpn.
, vol.62
, pp. 524-531
-
-
Aimoto, S.1
Mizoguchi, N.2
Hojo, H.3
Yoshimura, S.4
-
28
-
-
0036321730
-
Synthesis of amyloid β-peptides in solution employing chloroform-phenol mixed solvent for facile segment condensation of sparingly soluble protected peptides
-
Inui T, Bodi J, Nishio H, Nishiuchi Y, Kimura T. Synthesis of amyloid β-peptides in solution employing chloroform-phenol mixed solvent for facile segment condensation of sparingly soluble protected peptides. Lett. In Pep. Sci. 2001; 8: 319-330.
-
(2001)
Lett. In Pep. Sci.
, vol.8
, pp. 319-330
-
-
Inui, T.1
Bodi, J.2
Nishio, H.3
Nishiuchi, Y.4
Kimura, T.5
-
29
-
-
0005468127
-
A new one-pot method for Fmoc solution synthesis
-
Ueki M, Yanagihara T. A new one-pot method for Fmoc solution synthesis. Peptides 1998; 252-253.
-
(1998)
Peptides
, pp. 252-253
-
-
Ueki, M.1
Yanagihara, T.2
-
30
-
-
0014823090
-
Racemisietung bei Peptidesynthesen
-
Konig W, Geiger R. Racemisietung bei Peptidesynthesen. Chem. Ber. 1970; 103: 2024-2033.
-
(1970)
Chem. Ber.
, vol.103
, pp. 2024-2033
-
-
Konig, W.1
Geiger, R.2
-
31
-
-
0347991834
-
3-Hydroxy-4-oxo-3,4-dihydro-5-azabenzo-1,2,3-triazene
-
Carpino LA, Xia J, El-Faham A. 3-Hydroxy-4-oxo-3, 4-dihydro-5-azabenzo-1, 2, 3-triazene. J. Org. Chem. 2004; 69: 54-61.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 54-61
-
-
Carpino, L.A.1
Xia, J.2
El-Faham, A.3
-
32
-
-
0031012514
-
Efficient synthesis of peptaibol using a chloro imidazolidium coupling reagent, CIP
-
Akaji K, Tamai Y, Kiso Y. Efficient synthesis of peptaibol using a chloro imidazolidium coupling reagent, CIP. Tetrahedron 1997; 53: 567-584.
-
(1997)
Tetrahedron
, vol.53
, pp. 567-584
-
-
Akaji, K.1
Tamai, Y.2
Kiso, Y.3
-
33
-
-
33646728877
-
Insights into the mechanism and catalysis of the native chemical ligation reaction
-
Johnson EC, Kent SB. Insights into the mechanism and catalysis of the native chemical ligation reaction. J. Am. Chem. Soc. 2006; 128: 6640-6646.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 6640-6646
-
-
Johnson, E.C.1
Kent, S.B.2
-
34
-
-
0346150281
-
Effect of copper salts on peptide bond formation using peptide thioesters
-
Ingenito R, Wenschuh H. Effect of copper salts on peptide bond formation using peptide thioesters. Org. Lett. 2003; 5: 4587-4590.
-
(2003)
Org. Lett.
, vol.5
, pp. 4587-4590
-
-
Ingenito, R.1
Wenschuh, H.2
-
35
-
-
84867901293
-
Amide bond formation via pentafluorothiophenyl active esters
-
Davis AP, Walsh JJ. Amide bond formation via pentafluorothiophenyl active esters. Tetrahedron Lett. 2002; 43: 1487-1490.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 1487-1490
-
-
Davis, A.P.1
Walsh, J.J.2
-
36
-
-
79960594926
-
Fmoc synthesis of peptide thioesters without post-chain-assembly manipulation
-
Zheng JS, Chang HN, Wang FL, Liu L. Fmoc synthesis of peptide thioesters without post-chain-assembly manipulation. J. Am. Chem. Soc. 2011; 133: 11080-11083.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 11080-11083
-
-
Zheng, J.S.1
Chang, H.N.2
Wang, F.L.3
Liu, L.4
-
37
-
-
0033958539
-
Synthesis of a phosphorylated polypeptide by a thioester method
-
Kawakami T, Hasegawa K, Aimoto S. Synthesis of a phosphorylated polypeptide by a thioester method. Bull. Chem. Soc. Jpn. 2000; 73: 197-203.
-
(2000)
Bull. Chem. Soc. Jpn.
, vol.73
, pp. 197-203
-
-
Kawakami, T.1
Hasegawa, K.2
Aimoto, S.3
-
38
-
-
4444376263
-
Fmoc-based chemical synthesis and selective binding to super coiled DNA of the p53 C-terminal segment and its phosphorylated and acetylated derivatives
-
Teruya K, Murphy CA, Burlin T, Appella E, Mazur JS. Fmoc-based chemical synthesis and selective binding to super coiled DNA of the p53 C-terminal segment and its phosphorylated and acetylated derivatives. J. Pept. Sci. 2004; 10: 479-491.
-
(2004)
J. Pept. Sci.
, vol.10
, pp. 479-491
-
-
Teruya, K.1
Murphy, C.A.2
Burlin, T.3
Appella, E.4
Mazur, J.S.5
-
39
-
-
0030913561
-
Metal ion-assisted peptide cyclization
-
Zhang L, Tam JP. Metal ion-assisted peptide cyclization. Tetrahedron Lett. 1997; 38: 4375-4378.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 4375-4378
-
-
Zhang, L.1
Tam, J.P.2
|