-
1
-
-
33748369114
-
Methods and protocols of modern solid phase peptide synthesis
-
16946453 10.1385/MB:33:3:239 1:CAS:528:DC%2BD28XmvFygsb4%3D
-
Amblard M, Fehrentz JA, Martinez J, Subra G (2006) Methods and protocols of modern solid phase peptide synthesis. Mol Biotechnol 33(3):239-254
-
(2006)
Mol Biotechnol
, vol.33
, Issue.3
, pp. 239-254
-
-
Amblard, M.1
Fehrentz, J.A.2
Martinez, J.3
Subra, G.4
-
2
-
-
84890511080
-
Solid-phase peptide synthesis at elevated temperatures - A comparison of conventional and microwave heating technology
-
Bacsa B, Horvati K, Bosze S, Andreae F, Kappe CO (2008a) Solid-phase peptide synthesis at elevated temperatures - a comparison of conventional and microwave heating technology. J Pept Sci 14(8):73
-
(2008)
J Pept Sci
, vol.14
, Issue.8
, pp. 73
-
-
Bacsa, B.1
Horvati, K.2
Bosze, S.3
Andreae, F.4
Kappe, C.O.5
-
3
-
-
53049110370
-
Solid-phase synthesis of difficult peptide sequences at elevated temperatures: A critical comparison of microwave and conventional heating technologies
-
18729524 10.1021/jo8013897 1:CAS:528:DC%2BD1cXhtVChs7jF
-
Bacsa B, Horvati K, Bosze S, Andreae F, Kappe CO (2008b) Solid-phase synthesis of difficult peptide sequences at elevated temperatures: a critical comparison of microwave and conventional heating technologies. J Org Chem 73(19):7532-7542
-
(2008)
J Org Chem
, vol.73
, Issue.19
, pp. 7532-7542
-
-
Bacsa, B.1
Horvati, K.2
Bosze, S.3
Andreae, F.4
Kappe, C.O.5
-
4
-
-
0025767755
-
2-Chlorotrityl chloride resin - Studies on anchoring of Fmoc-Amino Acids and Peptide Cleavage
-
1:CAS:528:DyaK3MXltFGjur4%3D
-
Barlos K, Chatzi O, Gatos D, Stavropoulos G (1991) 2-Chlorotrityl chloride resin - studies on anchoring of Fmoc-Amino Acids and Peptide Cleavage. Int J Pept Prot Res 37(6):513-520
-
(1991)
Int J Pept Prot Res
, vol.37
, Issue.6
, pp. 513-520
-
-
Barlos, K.1
Chatzi, O.2
Gatos, D.3
Stavropoulos, G.4
-
5
-
-
0028220676
-
The role of solid-phase fragment condensation (Spfc) in peptide-synthesis
-
10.1055/s-1994-25472
-
Benz H (1994) The role of solid-phase fragment condensation (Spfc) in peptide-synthesis. Synth Stuttgart 4:337-358
-
(1994)
Synth Stuttgart
, vol.4
, pp. 337-358
-
-
Benz, H.1
-
6
-
-
0001420261
-
On the catalytic racemisation of amino acids and peptides
-
1:CAS:528:DyaB1MXhsVWhuw%3D%3D
-
Bergmann B, Zervas L (1928) On the catalytic racemisation of amino acids and peptides. Biochem Z 203:280-292
-
(1928)
Biochem Z
, vol.203
, pp. 280-292
-
-
Bergmann, B.1
Zervas, L.2
-
7
-
-
37049074206
-
A new reagent for the cleavage of fully protected peptides synthesized on 2-chlorotrityl chloride resin
-
10.1039/c39940002559
-
Bollhagen R, Schmiedberger M, Barlos K, Grell E (1994) A new reagent for the cleavage of fully protected peptides synthesized on 2-chlorotrityl chloride resin. J Chem Soc Chem Comm 22:2559-2560
-
(1994)
J Chem Soc Chem Comm
, vol.22
, pp. 2559-2560
-
-
Bollhagen, R.1
Schmiedberger, M.2
Barlos, K.3
Grell, E.4
-
8
-
-
37049046758
-
Tracer studies on Ester Hydrolysis.1. Triphenylmethyl acetate
-
Bunton CA, Konasiewicz A (1955) Tracer studies on Ester Hydrolysis.1. Triphenylmethyl acetate. J Chem Soc 1354-1359
-
(1955)
J Chem Soc
, pp. 1354-1359
-
-
Bunton, C.A.1
Konasiewicz, A.2
-
9
-
-
33750035585
-
Novel method for enhanced solid phase peptide synthesis using microwave energy
-
Collins JM, Collins MJ (2003) Novel method for enhanced solid phase peptide synthesis using microwave energy. Biopolymers 71(3):361
-
(2003)
Biopolymers
, vol.71
, Issue.3
, pp. 361
-
-
Collins, J.M.1
Collins, M.J.2
-
10
-
-
70349277032
-
COMU: A safer and more effective replacement for benzotriazole-based uronium coupling reagents
-
19621394 10.1002/chem.200900615 1:CAS:528:DC%2BD1MXhtFGlu7fO
-
El-Faham A, Funosas RS, Prohens R, Albericio F (2009) COMU: a safer and more effective replacement for benzotriazole-based uronium coupling reagents. Chem Eur J 15(37):9404-9416
-
(2009)
Chem Eur J
, vol.15
, Issue.37
, pp. 9404-9416
-
-
El-Faham, A.1
Funosas, R.S.2
Prohens, R.3
Albericio, F.4
-
12
-
-
0015492764
-
Carboxyl-catalyzed intramolecular aminolysis - Side reaction in solid-phase peptide synthesis
-
5032495 10.1021/ja00764a036 1:CAS:528:DyaE38XktlCqsLk%3D
-
Gisin BF, Merrifield RB (1972) Carboxyl-catalyzed intramolecular aminolysis - side reaction in solid-phase peptide synthesis. J Am Chem Soc 94(9):3102-3106
-
(1972)
J Am Chem Soc
, vol.94
, Issue.9
, pp. 3102-3106
-
-
Gisin, B.F.1
Merrifield, R.B.2
-
13
-
-
84890461673
-
O-Acyl isopeptide method: An efficient preparation of amyloidogenic peptide by use of racemization-free segment condensation
-
Higa A, Yoshiya T, Abe N, Fukao F, Kuruma T, Taniguchi A, Kimura T, Sohma Y, Kiso Y (2010) O-Acyl isopeptide method: an efficient preparation of amyloidogenic peptide by use of racemization-free segment condensation. J Pept Sci 16:59-60
-
(2010)
J Pept Sci
, vol.16
, pp. 59-60
-
-
Higa, A.1
Yoshiya, T.2
Abe, N.3
Fukao, F.4
Kuruma, T.5
Taniguchi, A.6
Kimura, T.7
Sohma, Y.8
Kiso, Y.9
-
14
-
-
0035051017
-
The 2-chlorotrityl resin: A worthy addition to the medicinal chemist's toolbox
-
11281850 10.2174/0929867013373192 1:CAS:528:DC%2BD3MXivVClt7c%3D
-
Hoekstra WJ (2001) The 2-chlorotrityl resin: a worthy addition to the medicinal chemist's toolbox. Curr Med Chem 8(6):715-719
-
(2001)
Curr Med Chem
, vol.8
, Issue.6
, pp. 715-719
-
-
Hoekstra, W.J.1
-
15
-
-
77954071086
-
Electrophilicity versus electrofugality of tritylium ions in aqueous acetonitrile
-
20496349 10.1002/chem.200902670 1:CAS:528:DC%2BC3cXot1als74%3D
-
Horn M, Mayr H (2010a) Electrophilicity versus electrofugality of tritylium ions in aqueous acetonitrile. Chem Eur J 16(25):7478-7487
-
(2010)
Chem Eur J
, vol.16
, Issue.25
, pp. 7478-7487
-
-
Horn, M.1
Mayr, H.2
-
16
-
-
77954065537
-
Stabilities of trityl-protected substrates: The wide mechanistic spectrum of trityl ester hydrolyses
-
20564285 10.1002/chem.200902669 1:CAS:528:DC%2BC3cXot1alsbY%3D
-
Horn M, Mayr H (2010b) Stabilities of trityl-protected substrates: the wide mechanistic spectrum of trityl ester hydrolyses. Chem Eur J 16(25):7469-7477
-
(2010)
Chem Eur J
, vol.16
, Issue.25
, pp. 7469-7477
-
-
Horn, M.1
Mayr, H.2
-
17
-
-
11144325118
-
Controlled microwave heating in modern organic synthesis
-
15558676 10.1002/anie.200400655 1:CAS:528:DC%2BD2cXhtFWrtL7O
-
Kappe CO (2004) Controlled microwave heating in modern organic synthesis. Angew Chem Int Ed Engl 43(46):6250-6284
-
(2004)
Angew Chem Int Ed Engl
, vol.43
, Issue.46
, pp. 6250-6284
-
-
Kappe, C.O.1
-
18
-
-
0027373903
-
Convergent solid-phase peptide-synthesis
-
10.1016/S0040-4020(01)81800-7 1:CAS:528:DyaK2cXnslKjug%3D%3D
-
Lloydwilliams P, Albericio F, Giralt E (1993) Convergent solid-phase peptide-synthesis. Tetrahedron 49(48):11065-11133
-
(1993)
Tetrahedron
, vol.49
, Issue.48
, pp. 11065-11133
-
-
Lloydwilliams, P.1
Albericio, F.2
Giralt, E.3
-
19
-
-
77956757211
-
Stereochemistry of amino acids
-
18884350 10.1016/S0065-3233(08)60009-1 1:CAS:528:DyaH1cXktF2hsw%3D%3D
-
Neuberger A (1948) Stereochemistry of amino acids. Adv Protein Chem 4:297-383
-
(1948)
Adv Protein Chem
, vol.4
, pp. 297-383
-
-
Neuberger, A.1
-
20
-
-
0031592560
-
A new approach to Hmb-backbone protection of peptides: Synthesis and reactivity of N-alpha-Fmoc-N-alpha-(Hmb)amino acids
-
10.1016/S0040-4039(97)00303-1 1:CAS:528:DyaK2sXis1ehsL8%3D
-
Nicolas E, Pujades M, Bacardit J, Giralt E, Albericio F (1997) A new approach to Hmb-backbone protection of peptides: synthesis and reactivity of N-alpha-Fmoc-N-alpha-(Hmb)amino acids. Tetrahedron Lett 38(13):2317-2320
-
(1997)
Tetrahedron Lett
, vol.38
, Issue.13
, pp. 2317-2320
-
-
Nicolas, E.1
Pujades, M.2
Bacardit, J.3
Giralt, E.4
Albericio, F.5
-
21
-
-
33947207869
-
Limiting racemization and aspartimide formation in microwave-enhanced Fmoc solid phase peptide synthesis
-
17121420 10.1002/psc.804 1:CAS:528:DC%2BD2sXjsVSgu7w%3D
-
Palasek SA, Cox ZJ, Collins JM (2007) Limiting racemization and aspartimide formation in microwave-enhanced Fmoc solid phase peptide synthesis. J Pept Sci 13(3):143-148
-
(2007)
J Pept Sci
, vol.13
, Issue.3
, pp. 143-148
-
-
Palasek, S.A.1
Cox, Z.J.2
Collins, J.M.3
-
22
-
-
84856834588
-
Microwave heating in solid-phase peptide synthesis
-
22012213 10.1039/c1cs15214a 1:CAS:528:DC%2BC38XitFyjsrk%3D
-
Pedersen SL, Tofteng AP, Malik L, Jensen KJ (2012) Microwave heating in solid-phase peptide synthesis. Chem Soc Rev 41(5):1826-1844
-
(2012)
Chem Soc Rev
, vol.41
, Issue.5
, pp. 1826-1844
-
-
Pedersen, S.L.1
Tofteng, A.P.2
Malik, L.3
Jensen, K.J.4
-
23
-
-
70349470853
-
Microwave irradiation and COMU: A potent combination for solid-phase peptide synthesis
-
10.1016/j.tetlet.2009.08.117 1:CAS:528:DC%2BD1MXhtF2gsrzL
-
Subiros-Funosas R, Acosta GA, El-Faham A, Albericio F (2009) Microwave irradiation and COMU: a potent combination for solid-phase peptide synthesis. Tetrahedron Lett 50(45):6200-6202
-
(2009)
Tetrahedron Lett
, vol.50
, Issue.45
, pp. 6200-6202
-
-
Subiros-Funosas, R.1
Acosta, G.A.2
El-Faham, A.3
Albericio, F.4
-
24
-
-
33947475846
-
Rates of solvolysis of triphenylmethyl acetate and fluoride. 2
-
10.1021/ja01508a031 1:CAS:528:DyaF3MXlvFensw%3D%3D
-
Swain CG, Knee TEC, Maclachlan A (1960) Rates of solvolysis of triphenylmethyl acetate and fluoride. 2. J Am Chem Soc 82(23):6101-6104
-
(1960)
J Am Chem Soc
, vol.82
, Issue.23
, pp. 6101-6104
-
-
Swain, C.G.1
Knee, T.E.C.2
Maclachlan, A.3
-
25
-
-
77957324874
-
Epimerization-free synthesis of cyclic peptide by use of the O-acyl isopeptide method
-
20623499 1:CAS:528:DC%2BC3cXpt1Crsrc%3D
-
Yoshiya T, Kawashima H, Hasegawa Y, Okamoto K, Kimura T, Sohma Y, Kiso Y (2010) Epimerization-free synthesis of cyclic peptide by use of the O-acyl isopeptide method. J Pept Sci 16(8):437-442
-
(2010)
J Pept Sci
, vol.16
, Issue.8
, pp. 437-442
-
-
Yoshiya, T.1
Kawashima, H.2
Hasegawa, Y.3
Okamoto, K.4
Kimura, T.5
Sohma, Y.6
Kiso, Y.7
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