-
1
-
-
20744456789
-
Solid phase peptide synthesis I. The synthesis of a tetrapeptide
-
Merrifield RB. Solid phase peptide synthesis I. The synthesis of a tetrapeptide. J. Am. Chem. Soc. 1963; 85: 2149-2154.
-
(1963)
J. Am. Chem. Soc.
, vol.85
, pp. 2149-2154
-
-
Merrifield, R.B.1
-
2
-
-
0001331728
-
Synthetic peptide vaccine design: Synthesis and properties of a high-density multiple antigenic peptide system
-
Tam JP. Synthetic peptide vaccine design: synthesis and properties of a high-density multiple antigenic peptide system. Proc. Natl. Acad. Sci. USA 1988; 85: 5409-5413.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 5409-5413
-
-
Tam, J.P.1
-
3
-
-
0001334464
-
Template-assembled synthetic proteins with four-helix-bundle topology. Total chemical synthesis and conformational studies
-
Mutter M, Tuchscherer GC, Miller C, Altmann KH, Carey RI, Wyss DF, Labhardt, AM, Rivier JE. Template-assembled synthetic proteins with four-helix-bundle topology. Total chemical synthesis and conformational studies. J. Am. Chem. Soc. 1992; 114: 1463-1470.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 1463-1470
-
-
Mutter, M.1
Tuchscherer, G.C.2
Miller, C.3
Altmann, K.H.4
Carey, R.I.5
Wyss, D.F.6
Labhardt, A.M.7
Rivier, J.E.8
-
4
-
-
33751500445
-
Evaluation of the oxime resin based segment synthesis-condensation approach using RNAse T1 as a model synthetic target
-
Sasaki T, Finderis MA, Kaiser ET. Evaluation of the oxime resin based segment synthesis-condensation approach using RNAse T1 as a model synthetic target. J. Org. Chem. 1991; 56: 3159-3168.
-
(1991)
J. Org. Chem.
, vol.56
, pp. 3159-3168
-
-
Sasaki, T.1
Finderis, M.A.2
Kaiser, E.T.3
-
5
-
-
0028231302
-
Formation of homogeneous artificial proteins
-
Rose K. Formation of homogeneous artificial proteins. J. Am. Chem. Soc. 1994; 116: 30-33.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 30-33
-
-
Rose, K.1
-
6
-
-
0027947767
-
Synthesis of peptide dendrimers
-
Tam JP, Rao C. Synthesis of peptide dendrimers. J. Am. Chem. Soc. 1994; 116: 6975-6976.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 6975-6976
-
-
Tam, J.P.1
Rao, C.2
-
7
-
-
0030724874
-
Multiple antigen peptide system
-
Tam JP, Spetzler JC. Multiple antigen peptide system. Methods Enzymol. 1997; 289: 612-637.
-
(1997)
Methods Enzymol.
, vol.289
, pp. 612-637
-
-
Tam, J.P.1
Spetzler, J.C.2
-
8
-
-
0033553118
-
Lactone and lactam library synthesis by silver ion-assisted orthogonal cyclization of unprotected peptides
-
Zhang LS, Tam JP. Lactone and lactam library synthesis by silver ion-assisted orthogonal cyclization of unprotected peptides. J. Am. Chem. Soc. 1999; 121: 3311-3320.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 3311-3320
-
-
Zhang, L.S.1
Tam, J.P.2
-
9
-
-
2442752591
-
Peptide and glycopeptide dendrimers. Part I
-
Veprek P, Jezek J. Peptide and glycopeptide dendrimers. Part I. J. Pep. Sci. 1999; 5: 5-23.
-
(1999)
J. Pep. Sci.
, vol.5
, pp. 5-23
-
-
Veprek, P.1
Jezek, J.2
-
10
-
-
2442727488
-
Peptide and glycopeptide dendrimers. Part II
-
Veprek P, Jezek J. Peptide and glycopeptide dendrimers. Part II. J. Pep. Sci. 1999; 5: 203-220.
-
(1999)
J. Pep. Sci.
, vol.5
, pp. 203-220
-
-
Veprek, P.1
Jezek, J.2
-
11
-
-
0028960723
-
Unprotected peptides as building blocks for the synthesis of peptide dendrimers with oxime, hydrazone and thiazolidine linkages
-
Shao J, Tam JP. Unprotected peptides as building blocks for the synthesis of peptide dendrimers with oxime, hydrazone and thiazolidine linkages. J. Am. Chem. Soc. 1995; 117: 3894-3899.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 3894-3899
-
-
Shao, J.1
Tam, J.P.2
-
12
-
-
0028886196
-
Cyclization of totally unprotected peptides in aqueous solution by oxime formation
-
Pallin TD, Tam JP. Cyclization of totally unprotected peptides In aqueous solution by oxime formation. J. Chem. Soc., Chem. Commun. 1995; 2021-2022.
-
(1995)
J. Chem. Soc., Chem. Commun.
, pp. 2021-2022
-
-
Pallin, T.D.1
Tam, J.P.2
-
14
-
-
0029790914
-
Synthesis of glycopeptides and lipopeptides by chemoselective ligation
-
Cervigni SE, Dumy P, Mutter M. Synthesis of glycopeptides and lipopeptides by chemoselective ligation. Angev. Chem., Int. Ed. Engl. 1996; 35: 1230-1232.
-
(1996)
Angev. Chem., Int. Ed. Engl.
, vol.35
, pp. 1230-1232
-
-
Cervigni, S.E.1
Dumy, P.2
Mutter, M.3
-
15
-
-
0026525457
-
Constructing proteins by dovetailing unprotected synthetic peptides: Backbone-engineered HIV protease
-
Schnolzer M, Kent SB. Constructing proteins by dovetailing unprotected synthetic peptides: backbone-engineered HIV protease. Science 1992; 256: 221-225.
-
(1992)
Science
, vol.256
, pp. 221-225
-
-
Schnolzer, M.1
Kent, S.B.2
-
16
-
-
0028301450
-
Design and chemical synthesis of a neoprotein structural model for the cytoplasmic domain of a multisubunit cell-surface receptor-integrin αIIb-β3 (platelet GPIIb-IIIa)
-
Muir TW, Williams MJ, Ginsberg MH, Kent SB. Design and chemical synthesis of a neoprotein structural model for the cytoplasmic domain of a multisubunit cell-surface receptor-integrin αIIb-β3 (platelet GPIIb-IIIa). Biochemistry 1994; 33: 7701-7708.
-
(1994)
Biochemistry
, vol.33
, pp. 7701-7708
-
-
Muir, T.W.1
Williams, M.J.2
Ginsberg, M.H.3
Kent, S.B.4
-
17
-
-
0000439676
-
Convenient total synthesis of a 4-helix tasp molecule by chemoselective ligation
-
Dawson PE, Kent SB. Convenient total synthesis of a 4-helix tasp molecule by chemoselective ligation. J. Am. Chem. Soc. 1993; 115: 7263-7266.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 7263-7266
-
-
Dawson, P.E.1
Kent, S.B.2
-
19
-
-
0032482508
-
A novel method to synthesize cyclic peptides
-
Shao Y, Lu WY, Kent SB. A novel method to synthesize cyclic peptides. Tetrahedron Lett. 1998; 39: 3911-3914.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 3911-3914
-
-
Shao, Y.1
Lu, W.Y.2
Kent, S.B.3
-
20
-
-
0033549108
-
Thia zip reaction for synthesis of large cyclic peptides: Mechanisms and applications
-
Tam JP, Lu Y-A, Yu Q. Thia zip reaction for synthesis of large cyclic peptides: mechanisms and applications. J. Am. Chem. Soc. 1999; 121: 4316-4324.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 4316-4324
-
-
Tam, J.P.1
Lu, Y.-A.2
Yu, Q.3
-
21
-
-
0031799735
-
Cyanocysteine-mediated molecular dissection of dihydrofolate reductase - Occurrence of Intramolecular and Intermolecular reactions forming a peptide bond
-
Takenawa T, Oda Y, Ishihama Y, Iwakura M. Cyanocysteine-mediated molecular dissection of dihydrofolate reductase - occurrence of Intramolecular and Intermolecular reactions forming a peptide bond. J. Biochem. 1998; 123: 1137-1144.
-
(1998)
J. Biochem.
, vol.123
, pp. 1137-1144
-
-
Takenawa, T.1
Oda, Y.2
Ishihama, Y.3
Iwakura, M.4
-
22
-
-
0033597333
-
A novel method for peptide block synthesis using unprotected peptides
-
Ishihama Y, Ito O, Oda Y, Takenawa T, Iwakura M. A novel method for peptide block synthesis using unprotected peptides. Tetrahedron Lett. 1999; 40: 3415-3418.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 3415-3418
-
-
Ishihama, Y.1
Ito, O.2
Oda, Y.3
Takenawa, T.4
Iwakura, M.5
-
23
-
-
0032192431
-
Chemoselective and stereoselective glycosylatlon of hydroxylamino derivatives - A versatile approach to glycoconjugates
-
Peri F, Dumy P, Mutter M. Chemoselective and stereoselective glycosylatlon of hydroxylamino derivatives - a versatile approach to glycoconjugates. Tetrahedron 1998; 54: 12269-12278.
-
(1998)
Tetrahedron
, vol.54
, pp. 12269-12278
-
-
Peri, F.1
Dumy, P.2
Mutter, M.3
-
24
-
-
1642616144
-
Synthesis of DL-Canaline and some of its derivatives
-
Knobler Y, Frankel M. Synthesis of DL-Canaline and some of its derivatives. J. Chem. Soc. 1958; 1632-1635.
-
(1958)
J. Chem. Soc.
, pp. 1632-1635
-
-
Knobler, Y.1
Frankel, M.2
-
25
-
-
0022871385
-
Synthesis of L-canaline and γ-functional 2-aminobutyric acid derivatives
-
Oziskas AJ, Rosenthal GA. Synthesis of L-canaline and γ-functional 2-aminobutyric acid derivatives. J. Org. Chem. 1986; 51: 5047-5050.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 5047-5050
-
-
Oziskas, A.J.1
Rosenthal, G.A.2
-
26
-
-
0031989019
-
Chemoselectively addressable HCan building blocks in peptide synthesis: L-homocanaline derivatives
-
Lang I, Donze N, Garrouste P, Dumy P, Mutter M. Chemoselectively addressable HCan building blocks in peptide synthesis: L-homocanaline derivatives. J. Pep. Sci. 1998; 4: 72-80.
-
(1998)
J. Pep. Sci.
, vol.4
, pp. 72-80
-
-
Lang, I.1
Donze, N.2
Garrouste, P.3
Dumy, P.4
Mutter, M.5
-
27
-
-
1642631524
-
β-Aminoxy-D-Alanine
-
Stammer CH. β-Aminoxy-D-Alanine. J. Org. Chem. 1962; 27: 2957-2958.
-
(1962)
J. Org. Chem.
, vol.27
, pp. 2957-2958
-
-
Stammer, C.H.1
-
28
-
-
1642600516
-
Hydroxylamines derivatives, communication 6. Synthesis and some reactions of 3-(aminooxy)alanine
-
Khomutov RM, Karpeiskii MY, Severin ES. Hydroxylamines derivatives, communication 6. Synthesis and some reactions of 3-(aminooxy)alanine. Bull. Acad. Sci. USSR, Div. Chem. Sci. 1964; 6: 631-634.
-
(1964)
Bull. Acad. Sci. USSR, Div. Chem. Sci.
, vol.6
, pp. 631-634
-
-
Khomutov, R.M.1
Karpeiskii, M.Y.2
Severin, E.S.3
-
30
-
-
0001041292
-
Synthesis of cycloserine and a methyl analog
-
Stammer CH, Wilson AN, Spencer CF, Bachelor FW, Holly FW, Folkers K. Synthesis of cycloserine and a methyl analog. J. Am. Chem. Soc. 1957; 79: 3236-3240.
-
(1957)
J. Am. Chem. Soc.
, vol.79
, pp. 3236-3240
-
-
Stammer, C.H.1
Wilson, A.N.2
Spencer, C.F.3
Bachelor, F.W.4
Holly, F.W.5
Folkers, K.6
-
31
-
-
0029866699
-
Efficient Mitsunobu reactions with N-phenylfluorenyl or N-trityl serine esters
-
Cherney RJ, Wang L. Efficient Mitsunobu reactions with N-phenylfluorenyl or N-trityl serine esters. J. Org. Chem. 1996; 61: 2544-2546.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 2544-2546
-
-
Cherney, R.J.1
Wang, L.2
-
33
-
-
85082716815
-
A novel synthesis of acyclic N-(αhydroxybenzyl)benzamides
-
Katritzky AR, Rao MSC. A novel synthesis of acyclic N-(αhydroxybenzyl)benzamides. Synthesis 1990; 663-666.
-
(1990)
Synthesis
, pp. 663-666
-
-
Katritzky, A.R.1
Rao, M.S.C.2
-
34
-
-
85007968665
-
Synthesis of tricholomic acid. VI. Synthesis of DL-tricholomic acid and its threo-isomer from diastereoisomers of β-hydroxyglutamic acid α-benzyl ester
-
Kamiya T. Synthesis of tricholomic acid. VI. Synthesis of DL-tricholomic acid and its threo-isomer from diastereoisomers of β-hydroxyglutamic acid α-benzyl ester. Chem. Pharm. Bull. 1969; 17: 886-889.
-
(1969)
Chem. Pharm. Bull.
, vol.17
, pp. 886-889
-
-
Kamiya, T.1
-
35
-
-
0030951249
-
Canavanine derivatives useful in peptide synthesis
-
Pajpanova T, Stoev S, Golovlnsky E, Krauss GJ, Mlersch J. Canavanine derivatives useful in peptide synthesis. Amino Acids 1997; 12: 191-204.
-
(1997)
Amino Acids
, vol.12
, pp. 191-204
-
-
Pajpanova, T.1
Stoev, S.2
Golovlnsky, E.3
Krauss, G.J.4
Mlersch, J.5
-
36
-
-
0022354620
-
Conversion of serine to stereochemically pure β-substituted α-amino acids via β-lactones
-
Arnold LD, Kalantar TH, Vederas JC. Conversion of serine to stereochemically pure β-substituted α-amino acids via β-lactones. J. Am. Chem. Soc. 1985; 107: 7109-7115.
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 7109-7115
-
-
Arnold, L.D.1
Kalantar, T.H.2
Vederas, J.C.3
-
38
-
-
0000242199
-
Conversion of serine β-lactones to chiral α-amino acids by copper-containing organolithium and organomagnesium reagents
-
Arnold LD, Drover JCG, Vederas JC. Conversion of serine β-lactones to chiral α-amino acids by copper-containing organolithium and organomagnesium reagents. J. Am. Chem. Soc. 1987; 109: 4659.
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 4659
-
-
Arnold, L.D.1
Drover, J.C.G.2
Vederas, J.C.3
-
39
-
-
0026462905
-
A short synthesis of (S) - 3 - (dimethylphosphono) - 2 - ((9 - fluorenyl)methoxy-carbamoyl)propionic acid, a protected phosphonic acid analogue of aspartic acid
-
Hutchinson JPE, Parkes KEB. A short synthesis of (S) - 3 - (dimethylphosphono) - 2 - ((9 - fluorenyl)methoxy-carbamoyl)propionic acid, a protected phosphonic acid analogue of aspartic acid. Tetrahedron Lett. 1992; 33: 7065-7066.
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 7065-7066
-
-
Hutchinson, J.P.E.1
Parkes, K.E.B.2
-
40
-
-
0032499093
-
Incorporation of a phosphonic acid isostere of aspartic acid into peptides using Fmoc-solid phase synthesis
-
Lohse PA, Felber R. Incorporation of a phosphonic acid isostere of aspartic acid into peptides using Fmoc-solid phase synthesis. Tetrahedron Lett. 1998; 39: 2067-2070.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 2067-2070
-
-
Lohse, P.A.1
Felber, R.2
-
41
-
-
0027996185
-
Reaction of trimethylsilylamines with N-Cbz-L-serine-β-lactone - A convenient route to optically pure β-amino-L-alanine derivatives
-
Ratemi ES, Vederas JC. Reaction of trimethylsilylamines with N-Cbz-L-serine-β-lactone - a convenient route to optically pure β-amino-L-alanine derivatives. Tetrahedron Lett. 1994; 35: 7605-7608.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 7605-7608
-
-
Ratemi, E.S.1
Vederas, J.C.2
-
42
-
-
33947457900
-
β-Propiolactone XI
-
Gresham TL, Jansen JE, Shaver FW, Bankert RA, Feidorek FT. β-Propiolactone XI. J. Am. Chem. Soc. 1951; 73: 3168-3171.
-
(1951)
J. Am. Chem. Soc.
, vol.73
, pp. 3168-3171
-
-
Gresham, T.L.1
Jansen, J.E.2
Shaver, F.W.3
Bankert, R.A.4
Feidorek, F.T.5
-
43
-
-
0343247601
-
Synthesis of an aminopyrazolidine substituted quinolone acid
-
Kim KS, Ryan PC. Synthesis of an aminopyrazolidine substituted quinolone acid. Heterocycles 1990; 31: 79-86.
-
(1990)
Heterocycles
, vol.31
, pp. 79-86
-
-
Kim, K.S.1
Ryan, P.C.2
-
44
-
-
0028324801
-
Synthesis of chiral isoxazolidin-5-ones and their applications to the synthesis of β-amino-alanines and β-(N-hydroxy-amino)-alanines
-
Baldwin JE, Adlington RM, Mellor LC. Synthesis of chiral isoxazolidin-5-ones and their applications to the synthesis of β-amino-alanines and β-(N-hydroxy-amino)-alanines. Tetrahedron 1994; 50: 5049-5066.
-
(1994)
Tetrahedron
, vol.50
, pp. 5049-5066
-
-
Baldwin, J.E.1
Adlington, R.M.2
Mellor, L.C.3
-
46
-
-
0019169515
-
Preparation and properties of O-amino-D-serine; acid hydrolysis of D-4-amino-3-isoxazolidinone (D-cycloserine)
-
Korpela T, Makela M. Preparation and properties of O-amino-D-serine; acid hydrolysis of D-4-amino-3-isoxazolidinone (D-cycloserine). Synthesis 1980; 997-998.
-
(1980)
Synthesis
, pp. 997-998
-
-
Korpela, T.1
Makela, M.2
-
47
-
-
1642616139
-
Synthesis of an aminoisoxazolidine substituted quinolone acid
-
Kim KS. Synthesis of an aminoisoxazolidine substituted quinolone acid. Heterocycles 1990; 31: 87-95.
-
(1990)
Heterocycles
, vol.31
, pp. 87-95
-
-
Kim, K.S.1
-
50
-
-
0022635491
-
Immuno-modulating properties of the uremic pentapeptide H-Asp-Leu-Trp-Gly-Lys-OH
-
Niese D, Gilsdorf K, Hiester E, Dressen P, Michels S, Dengler HJ. Immuno-modulating properties of the uremic pentapeptide H-Asp-Leu-Trp-Gly-Lys-OH. Klin. Wochenschr. 1986; 64: 642-647.
-
(1986)
Klin. Wochenschr.
, vol.64
, pp. 642-647
-
-
Niese, D.1
Gilsdorf, K.2
Hiester, E.3
Dressen, P.4
Michels, S.5
Dengler, H.J.6
-
51
-
-
0018085515
-
Solid-phase peptide synthesis using mild base cleavage of N-fluorenylmethyloxycarbonyl amino acids
-
Chang CD, Meinhofer J. Solid-phase peptide synthesis using mild base cleavage of N-fluorenylmethyloxycarbonyl amino acids. Int. J. Pep. Prot. Res. 1978; 11: 246-249.
-
(1978)
Int. J. Pep. Prot. Res.
, vol.11
, pp. 246-249
-
-
Chang, C.D.1
Meinhofer, J.2
-
52
-
-
37049100132
-
A mild procedure for solid-phase peptide synthesis: Use of fluorenylmethyloxycarbonyl amino acids
-
Atheron E, Fox H, Harkiss D, Logan CJ, Sheppard RC, Williams BJ. A mild procedure for solid-phase peptide synthesis: use of fluorenylmethyloxycarbonyl amino acids. J. Chem. Soc., Chem. Commun. 1978; 537-539.
-
(1978)
J. Chem. Soc., Chem. Commun.
, pp. 537-539
-
-
Atheron, E.1
Fox, H.2
Harkiss, D.3
Logan, C.J.4
Sheppard, R.C.5
Williams, B.J.6
-
53
-
-
45949123116
-
Synthesis of protected peptide fragments using a trialkoxy-diphenyl-methyl ester resin
-
Rink H. Synthesis of protected peptide fragments using a trialkoxy-diphenyl-methyl ester resin. Tetrahedron Lett. 1987; 28: 3787-3790.
-
(1987)
Tetrahedron Lett.
, vol.28
, pp. 3787-3790
-
-
Rink, H.1
-
54
-
-
12044258245
-
1-Hydroxy-7-azabenzotriazole - An efficient peptide coupling additive
-
Carpino LA. 1-Hydroxy-7-azabenzotriazole - an efficient peptide coupling additive. J. Am. Chem. Soc. 1993; 115: 4397-4398.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 4397-4398
-
-
Carpino, L.A.1
-
55
-
-
0001151375
-
Noninvasive continuous monitoring of solid phase peptide synthesis by acid-base Indicator
-
Krchnak V, Vagner J, Safar S, Lebl M. Noninvasive continuous monitoring of solid phase peptide synthesis by acid-base Indicator. Collect. Czech. Chem. Commun. 1988; 53: 2542-2548.
-
(1988)
Collect. Czech. Chem. Commun.
, vol.53
, pp. 2542-2548
-
-
Krchnak, V.1
Vagner, J.2
Safar, S.3
Lebl, M.4
-
56
-
-
0032564564
-
Combinatorial chemistry of natural products: Solid phase synthesis of D- and L-cycloserine derivatives
-
Gordeev MI, Luehr GW, Hui HC, Gordon EM, Patel DV. Combinatorial chemistry of natural products: solid phase synthesis of D- and L-cycloserine derivatives. Tetrahedron 1998; 54: 15879-15890.
-
(1998)
Tetrahedron
, vol.54
, pp. 15879-15890
-
-
Gordeev, M.I.1
Luehr, G.W.2
Hui, H.C.3
Gordon, E.M.4
Patel, D.V.5
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