-
1
-
-
79952271952
-
Integrated SPPS on continuous-flow radial microfluidic chip
-
Wang W, Huang Y, Liu J, Xie Y, Zhao R, Xiong S, Liu G, Chen Y, Ma H. Integrated SPPS on continuous-flow radial microfluidic chip. Lab Chip 2011; 11: 929-935.
-
(2011)
Lab Chip
, vol.11
, pp. 929-935
-
-
Wang, W.1
Huang, Y.2
Liu, J.3
Xie, Y.4
Zhao, R.5
Xiong, S.6
Liu, G.7
Chen, Y.8
Ma, H.9
-
2
-
-
62449152302
-
Amide bond formation: beyond the myth of coupling reagents
-
Valeur E, Bradley M. Amide bond formation: beyond the myth of coupling reagents. Chem. Soc. Rev. 2009; 38: 606-631.
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 606-631
-
-
Valeur, E.1
Bradley, M.2
-
3
-
-
80755177032
-
Peptide coupling reagents, more than a letter soup
-
El-Faham A, Albericio F. Peptide coupling reagents, more than a letter soup. Chem. Rev. 2011; 111: 6557-6602.
-
(2011)
Chem. Rev.
, vol.111
, pp. 6557-6602
-
-
El-Faham, A.1
Albericio, F.2
-
5
-
-
77953946318
-
Umpolung reactivity in amide and peptide synthesis
-
Shen B, Makley DM, Johnston JM. Umpolung reactivity in amide and peptide synthesis. Nature 2010; 465: 1027-1033.
-
(2010)
Nature
, vol.465
, pp. 1027-1033
-
-
Shen, B.1
Makley, D.M.2
Johnston, J.M.3
-
6
-
-
84863011662
-
Expanding the limits of isonitrile-mediated amidations: on the remarkable stereosubtleties of macrolactam formation from synthetic seco-cyclosporins
-
Wu X, Stockdill JL, Park PK, Danishefsky SJ. Expanding the limits of isonitrile-mediated amidations: on the remarkable stereosubtleties of macrolactam formation from synthetic seco-cyclosporins. J. Am. Chem. Soc. 2012; 134: 2378-2384.
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 2378-2384
-
-
Wu, X.1
Stockdill, J.L.2
Park, P.K.3
Danishefsky, S.J.4
-
7
-
-
41649091460
-
Morpholine-based immonium and halogenoamidinium salts as coupling reagents in peptide synthesis
-
El-Faham A, Albericio F. Morpholine-based immonium and halogenoamidinium salts as coupling reagents in peptide synthesis. J. Org. Chem. 2008; 73: 2731-2737.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 2731-2737
-
-
El-Faham, A.1
Albericio, F.2
-
8
-
-
85055771088
-
A new coupling reagent for peptide synthesis
-
DE 90-4016596.
-
Breipohl G, Koenig W. A new coupling reagent for peptide synthesis. Ger. Offen. DE 90-4016596. 1991.
-
(1991)
Ger. Offen.
-
-
Breipohl, G.1
Koenig, W.2
-
10
-
-
70349275493
-
Oxyma: an efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosion
-
Subirós-Funosas R, Prohens R, Barbas R, El-Faham A, Albericio F. Oxyma: an efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosion. Chem. Eur. J. 2009; 15: 9394-9403.
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 9394-9403
-
-
Subirós-Funosas, R.1
Prohens, R.2
Barbas, R.3
El-Faham, A.4
Albericio, F.5
-
11
-
-
84890950901
-
Oxyma-based reagents for assisting acylation reactions in peptide and organic chemistry
-
accepted.
-
Subirós-Funosas R, Khattab SN, Nieto-Rodriguez L, El-Faham A, Albericio F. Oxyma-based reagents for assisting acylation reactions in peptide and organic chemistry. Aldrichim. Acta. 2013, accepted.
-
(2013)
Aldrichim. Acta.
-
-
Subirós-Funosas, R.1
Khattab, S.N.2
Nieto-Rodriguez, L.3
El-Faham, A.4
Albericio, F.5
-
12
-
-
84875737690
-
Ethyl 2-(tert-butoxycarbonyloxyimino)-2-cyanoacetate(Boc-Oxyma) as coupling reagent for racemization-free esterification, thioesterification, amidation and peptide synthesis
-
Thalluri K, Nadimpally KC, Chakravarty MP, Paul A, Mandal B. Ethyl 2-(tert-butoxycarbonyloxyimino)-2-cyanoacetate(Boc-Oxyma) as coupling reagent for racemization-free esterification, thioesterification, amidation and peptide synthesis. Adv. Synth. Catal. 2013; 355: 448-462
-
(2013)
Adv. Synth. Catal.
, vol.355
, pp. 448-462
-
-
Thalluri, K.1
Nadimpally, K.C.2
Chakravarty, M.P.3
Paul, A.4
Mandal, B.5
-
13
-
-
70349277032
-
COMU: a safer and more effective replacement for benzotriazole-based uronium coupling reagents
-
El-Faham A, Subirós-Funosas R, Prohens R, Albericio F. COMU: a safer and more effective replacement for benzotriazole-based uronium coupling reagents. Chem. Eur. J. 2009; 15: 9404-9416.
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 9404-9416
-
-
El-Faham, A.1
Subirós-Funosas, R.2
Prohens, R.3
Albericio, F.4
-
14
-
-
84878999406
-
-
Peptides: building bridges. The Proceedings of the 22nd American Peptide Symposium, Ed: Lebl M.) American Peptide Society
-
Behrend R, Brünner A, White P. Peptides: building bridges. The Proceedings of the 22nd American Peptide Symposium, (Ed: Lebl M.) American Peptide Society, 2011, 12-13.
-
(2011)
, pp. 12-13
-
-
Behrend, R.1
Brünner, A.2
White, P.3
-
15
-
-
78650229299
-
An expedient conversion of α-amino acids into Weinreb amides using COMU as a coupling agent
-
Tyrrell E, Brawn P, Carew M, Greenwood I. An expedient conversion of α-amino acids into Weinreb amides using COMU as a coupling agent. Tetrahedron Lett. 2011; 52: 369-372.
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 369-372
-
-
Tyrrell, E.1
Brawn, P.2
Carew, M.3
Greenwood, I.4
-
16
-
-
84865958885
-
Optimized synthesis and characterization of N-acylethanolamines and O-acylethanolamines, important family of lipid-signalling molecules
-
Ottria R, Casati S, Ciuffreda P. Optimized synthesis and characterization of N-acylethanolamines and O-acylethanolamines, important family of lipid-signalling molecules. Chem. Phys. Lipids 2012; 165: 705-711.
-
(2012)
Chem. Phys. Lipids
, vol.165
, pp. 705-711
-
-
Ottria, R.1
Casati, S.2
Ciuffreda, P.3
-
17
-
-
0036462499
-
The uronium/guanidinium peptide coupling reagents: finally the true uronium salts
-
Carpino LA, Imazumi H, El-Faham A, Ferrer FJ, Zhang C, Lee Y, Foxman BM, Henklein P, Hanay C, Mügge C, Wenschuh H, Klose J, Beyermann M, Bienert M. The uronium/guanidinium peptide coupling reagents: finally the true uronium salts. Angew. Chem. Int. Ed. 2002; 41(3): 441-445.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, Issue.3
, pp. 441-445
-
-
Carpino, L.A.1
Imazumi, H.2
El-Faham, A.3
Ferrer, F.J.4
Zhang, C.5
Lee, Y.6
Foxman, B.M.7
Henklein, P.8
Hanay, C.9
Mügge, C.10
Wenschuh, H.11
Klose, J.12
Beyermann, M.13
Bienert, M.14
-
18
-
-
84862742681
-
Bioactive mesoglobules of poly(di(ethylene glycol) monomethyl ether methacrylate)-peptide conjugate
-
Trzcinska R, Szweda D, Rangelov S, Suder P, Silberring J, Dworak A, Trzebicka B. Bioactive mesoglobules of poly(di(ethylene glycol) monomethyl ether methacrylate)-peptide conjugate. J. Polym. Sci. A: Polym. Chem. 2012; 50: 3104-3115.
-
(2012)
J. Polym. Sci. A: Polym. Chem.
, vol.50
, pp. 3104-3115
-
-
Trzcinska, R.1
Szweda, D.2
Rangelov, S.3
Suder, P.4
Silberring, J.5
Dworak, A.6
Trzebicka, B.7
-
19
-
-
84859624519
-
Enhanced epimerization of glycosylated amino acids during solid- phase peptide synthesis
-
Zhang Y, Muthana SM, Farnsworth D, Ludek O, Adams K, Barchi JrJJ, Gildersleeve JC. Enhanced epimerization of glycosylated amino acids during solid- phase peptide synthesis. J. Am. Chem. Soc. 2012; 134: 6316-6325.
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 6316-6325
-
-
Zhang, Y.1
Muthana, S.M.2
Farnsworth, D.3
Ludek, O.4
Adams, K.5
Barchi, J.6
Gildersleeve, J.C.7
-
20
-
-
84856115671
-
Solid-phase synthesis of NMe-IB-01212, a highly N-methylated cyclic peptide
-
Marcucci E, Tulla-Puche J, Albericio F. Solid-phase synthesis of NMe-IB-01212, a highly N-methylated cyclic peptide. Org. Lett. 2012; 14(2): 612-615.
-
(2012)
Org. Lett.
, vol.14
, Issue.2
, pp. 612-615
-
-
Marcucci, E.1
Tulla-Puche, J.2
Albericio, F.3
-
21
-
-
79955921951
-
Structural mimicry of the α-helix in aqueous solution with an isoatomic α/β/γ-peptide backbone
-
Sawada T, Gellman SH. Structural mimicry of the α-helix in aqueous solution with an isoatomic α/β/γ-peptide backbone. J. Am. Chem. Soc. 2011; 133: 7336-7339.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 7336-7339
-
-
Sawada, T.1
Gellman, S.H.2
-
22
-
-
84862089672
-
Chemical protein synthesis by chemoselective a-ketoacid- hydroxylamine (KAHA) ligations with 5-oxaproline
-
Pattabiraman VR, Ogunkoya AO, Bode JW. Chemical protein synthesis by chemoselective a-ketoacid- hydroxylamine (KAHA) ligations with 5-oxaproline. Angew. Chem. Int. Ed. 2012; 51: 5114-5118.
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 5114-5118
-
-
Pattabiraman, V.R.1
Ogunkoya, A.O.2
Bode, J.W.3
-
23
-
-
81355160960
-
Improving the Fmoc solid phase synthesis of the cyclic hexapeptide complement C5a antagonist, PMX205
-
deLisle Milton RC
-
deLisle Milton RC, Milton SC, Chamberlin AR. Improving the Fmoc solid phase synthesis of the cyclic hexapeptide complement C5a antagonist, PMX205. Int. J. Pept. Res. Ther. 2011; 17: 337-342.
-
(2011)
Int. J. Pept. Res. Ther
, vol.17
, pp. 337-342
-
-
Milton, S.C.1
Chamberlin, A.R.2
-
24
-
-
84856227484
-
Efficient solid-phase synthesis of cyclic RGD peptides under controlled
-
Yamada K, Nagashima I, Hachisu M, Matsuo I, Shimizu H. Efficient solid-phase synthesis of cyclic RGD peptides under controlled. Tetrahedron Lett. 2012; 53: 1066-1070.
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 1066-1070
-
-
Yamada, K.1
Nagashima, I.2
Hachisu, M.3
Matsuo, I.4
Shimizu, H.5
-
25
-
-
79960575010
-
Expedient solution-phase synthesis and NMR studies of arylopeptoids
-
Hjelmgaard T, Faure S, Staerk D, Taillefumier C, Nielsen J. Expedient solution-phase synthesis and NMR studies of arylopeptoids. Eur. J. Org. Chem. 2011; 4121-4132.
-
(2011)
Eur. J. Org. Chem.
, pp. 4121-4132
-
-
Hjelmgaard, T.1
Faure, S.2
Staerk, D.3
Taillefumier, C.4
Nielsen, J.5
-
26
-
-
80052783851
-
Efficient and versatile COMU-mediated solid-phase submonomer synthesis of arylopeptoids (oligomeric N-substituted aminomethyl benzamides)
-
Hjelmgaard T, Faure S, Staerk D, Taillefumier C, Nielsen J. Efficient and versatile COMU-mediated solid-phase submonomer synthesis of arylopeptoids (oligomeric N-substituted aminomethyl benzamides). Org. Biomol. Chem. 2011; 9: 6832-6843.
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 6832-6843
-
-
Hjelmgaard, T.1
Faure, S.2
Staerk, D.3
Taillefumier, C.4
Nielsen, J.5
-
27
-
-
84878962803
-
-
Peptide modifications at the C-terminus in solid phase synthesis with side chain peptide attachment onto chlorotrityl resin. Peptides: building bridges. The Proceedings of the 22nd American Peptide Symposium, Ed: Lebl M.) American Peptide Society
-
Kwiatkowska A, Bonin M-A, Yuan XW, Neugebauer WA. Peptide modifications at the C-terminus in solid phase synthesis with side chain peptide attachment onto chlorotrityl resin. Peptides: building bridges. The Proceedings of the 22nd American Peptide Symposium, (Ed: Lebl M.) American Peptide Society, 2011, 20-21.
-
(2011)
, pp. 20-21
-
-
Kwiatkowska, A.1
Bonin, M.-A.2
Yuan, X.W.3
Neugebauer, W.A.4
-
28
-
-
84857505914
-
Evaluation of COMU as a coupling reagent for in situ neutralization Boc solid phase peptide synthesis
-
Hjørringgaard CU, Brust A, Alewood PF. Evaluation of COMU as a coupling reagent for in situ neutralization Boc solid phase peptide synthesis. J. Pept. Sci. 2012; 18: 199-207.
-
(2012)
J. Pept. Sci.
, vol.18
, pp. 199-207
-
-
Hjørringgaard, C.U.1
Brust, A.2
Alewood, P.F.3
-
30
-
-
84861078289
-
Optimization of adenosine 5′-carboxamide derivatives as adenosine receptor agonists using structure-based ligand design and fragment screening
-
Tosh DK, Phan K, Gao Z-G, Gakh AA, Xu F, Deflorian F, Abagyan R, Stevens RC, Jacobson KA, Katritch V. Optimization of adenosine 5′-carboxamide derivatives as adenosine receptor agonists using structure-based ligand design and fragment screening. J. Med. Chem. 2012; 55(9): 4297-4308.
-
(2012)
J. Med. Chem.
, vol.55
, Issue.9
, pp. 4297-4308
-
-
Tosh, D.K.1
Phan, K.2
Gao, Z.-G.3
Gakh, A.A.4
Xu, F.5
Deflorian, F.6
Abagyan, R.7
Stevens, R.C.8
Jacobson, K.A.9
Katritch, V.10
-
31
-
-
84872056229
-
New 2,3-diaminopropionic acid inhibitors of AGE and ALE formation
-
Audic N, Potier G, Sasaki NA. New 2, 3-diaminopropionic acid inhibitors of AGE and ALE formation. Org. Biomol. Chem. 2013; 11: 773-780.
-
(2013)
Org. Biomol. Chem.
, vol.11
, pp. 773-780
-
-
Audic, N.1
Potier, G.2
Sasaki, N.A.3
-
32
-
-
84874450375
-
Evaluation of alternative solvents in common amide coupling reactions: replacement of dichloromethane and N,N-dimethylformamide
-
MacMillan DS, Murray J, Sneddon HF, Jamieson C, Watson AJB. Evaluation of alternative solvents in common amide coupling reactions: replacement of dichloromethane and N, N-dimethylformamide. Green Chem. 2013; 15: 596-600. Kusuma BR, Brandt GEL, Blagg BSJ. Synthesis of cruentaren A. Org. Lett. 2012; 14 (24): 6242-6245.
-
(2012)
Green Chem. 2013; 15: 596-600. , , . Synthesis of cruentaren A. Org. Lett.
, vol.14
, Issue.24
, pp. 6242-6245
-
-
MacMillan, D.S.1
Murray, J.2
Sneddon, H.F.3
Jamieson, C.4
Watson, A.J.B.5
Kusuma, B.R.6
Brandt, G.E.L.7
Blagg, B.S.J.8
-
33
-
-
84878958271
-
-
US 20110092676 A1 20110421, U.S. Pat. Appl. Publ. ().
-
Della Ciana, L. US 20110092676 A1 20110421, U.S. Pat. Appl. Publ. (2011).
-
(2011)
-
-
Della Ciana, L.1
-
34
-
-
84655169565
-
LDV peptidomimetics equipped with biotinylated spacer-arms: synthesis and biological evaluation on CCRF-CEM cell line
-
Gérard E, Meulle A, Feron O, Marchand-Brynaert J. LDV peptidomimetics equipped with biotinylated spacer-arms: synthesis and biological evaluation on CCRF-CEM cell line. Bioorg. Med. Chem. Lett. 2012; 22: 586-590.
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 586-590
-
-
Gérard, E.1
Meulle, A.2
Feron, O.3
Marchand-Brynaert, J.4
-
35
-
-
80054768881
-
Monoenomycin: a simplified trienomycin A analogue that manifests anticancer activity
-
Brandt GEL, Bragg BSJ. Monoenomycin: a simplified trienomycin A analogue that manifests anticancer activity. ACS Med. Chem. Lett. 2011; 2: 735-740.
-
(2011)
ACS Med. Chem. Lett.
, vol.2
, pp. 735-740
-
-
Brandt, G.E.L.1
Bragg, B.S.J.2
-
36
-
-
84867733043
-
Enantioselective total synthesis of the mexicanolides: khayasin, proceranolide, and mexicanolide
-
Faber JM, Eger WA, Williams CM. Enantioselective total synthesis of the mexicanolides: khayasin, proceranolide, and mexicanolide. J. Org. Chem. 2012; 77: 8913-8921.
-
(2012)
J. Org. Chem.
, vol.77
, pp. 8913-8921
-
-
Faber, J.M.1
Eger, W.A.2
Williams, C.M.3
-
37
-
-
84872813348
-
Ionic liquid mediated synthesis of peptide nucleic acids dimers
-
Poletti L, Giannini C. Ionic liquid mediated synthesis of peptide nucleic acids dimers. Tetrahedron 2013; 69: 1940-1944.
-
(2013)
Tetrahedron
, vol.69
, pp. 1940-1944
-
-
Poletti, L.1
Giannini, C.2
-
38
-
-
84873049851
-
Design and synthesis of nucleoproline amino acids for the straightforward preparation of chiral and conformationally constrained nucleopeptides
-
Kramer RA, Bleicher KH, Wennemers H. Design and synthesis of nucleoproline amino acids for the straightforward preparation of chiral and conformationally constrained nucleopeptides. Helv. Chim. Acta 2012; 95: 2621-2634.
-
(2012)
Helv. Chim. Acta
, vol.95
, pp. 2621-2634
-
-
Kramer, R.A.1
Bleicher, K.H.2
Wennemers, H.3
-
39
-
-
84875206835
-
-
Cao B, Chen X, Yamaryo-Botte Y, Richardson MB, Martin KL. J. Org. Chem. 2013; 78: 2175-2190.
-
(2013)
J. Org. Chem.
, vol.78
, pp. 2175-2190
-
-
Cao, B.1
Chen, X.2
Yamaryo-Botte, Y.3
Richardson, M.B.4
Martin, K.L.5
-
40
-
-
79958797659
-
Efficient and controllably selective preparation of esters using uronium-based coupling agents
-
Twibanire J-AK, Grindley TB. Efficient and controllably selective preparation of esters using uronium-based coupling agents. Org. Lett. 2011; 13: 2988-2991.
-
(2011)
Org. Lett.
, vol.13
, pp. 2988-2991
-
-
Twibanire, J.-A.1
Grindley, T.B.2
-
41
-
-
84863653629
-
Effect of residual water and microwave heating on the half-life of the reagents and reactive intermediates in peptide synthesis
-
Tofteng AP, Pedersen SL, Staerk D, Jensen KJ. Effect of residual water and microwave heating on the half-life of the reagents and reactive intermediates in peptide synthesis. Chem. Eur. J. 2012; 18(29):9024-9031.
-
(2012)
Chem. Eur. J.
, vol.18
, Issue.29
, pp. 9024-9031
-
-
Tofteng, A.P.1
Pedersen, S.L.2
Staerk, D.3
Jensen, K.J.4
-
42
-
-
84870603878
-
Microwave heating in solid-phase synthesis of N-methylated peptides: when is room temperature better?
-
Roodbeen R, Pedersen SL, Hosseini M, Jensen KJ, Microwave heating in solid-phase synthesis of N-methylated peptides: when is room temperature better? Eur. J. Org. Chem. 2012; 7106-7111.
-
(2012)
Eur. J. Org. Chem.
, pp. 7106-7111
-
-
Roodbeen, R.1
Pedersen, S.L.2
Hosseini, M.3
Jensen, K.J.4
-
43
-
-
84941316294
-
-
Peptides: building bridges. The Proceedings of the 22nd American Peptide Symposium,(Ed: Lebl M.) American Peptide Society
-
Nieto-Rodriguez L, Carceller M, Subirós-Funosas R, Acosta GA, Paradís Bas M, El-Faham A, Albericio F. Peptides: building bridges. The Proceedings of the 22nd American Peptide Symposium, (Ed: Lebl M.) American Peptide Society, 2011, 16-17.
-
(2011)
, pp. 16-17
-
-
Nieto-Rodriguez, L.1
Carceller, M.2
Subirós-Funosas, R.3
Acosta, G.A.4
Paradís Bas, M.5
El-Faham, A.6
Albericio, F.7
-
45
-
-
77957297577
-
Automated 'X-Y' robot for peptide synthesis with microwave heating: application to difficult peptide sequences and protein domains
-
Malik L, Tofteng AP, Pedersen SL, Sørensen KK, Jensen KJ. Automated 'X-Y' robot for peptide synthesis with microwave heating: application to difficult peptide sequences and protein domains. J. Pept. Sci. 2010; 16: 506-512.
-
(2010)
J. Pept. Sci.
, vol.16
, pp. 506-512
-
-
Malik, L.1
Tofteng, A.P.2
Pedersen, S.L.3
Sørensen, K.K.4
Jensen, K.J.5
-
46
-
-
84878962201
-
Microwave heating in solid-phase peptide synthesis
-
Tofteng AP, Malik L, Pedersen SL, Sørensen KK, Jensen KJ. Microwave heating in solid-phase peptide synthesis. Chim. Oggi 2011; 29: 12-15.
-
(2011)
Chim. Oggi
, vol.29
, pp. 12-15
-
-
Tofteng, A.P.1
Malik, L.2
Pedersen, S.L.3
Sørensen, K.K.4
Jensen, K.J.5
-
47
-
-
84878966778
-
-
Automated microwave-assisted SPPS: synthesis of N-methylated peptides, Aib sequences, and 'Difficult' sequences. Poster presented at the 22nd American Peptide Symposium, American Peptide Society, P041.
-
Pedersen SL, Jensen KJ. Automated microwave-assisted SPPS: synthesis of N-methylated peptides, Aib sequences, and 'Difficult' sequences. Poster presented at the 22nd American Peptide Symposium, American Peptide Society, 2011, P041.
-
(2011)
-
-
Pedersen, S.L.1
Jensen, K.J.2
-
48
-
-
84879000805
-
-
Systematic study of the SPPS of sterically hindered N-methylated peptides using microwave heating. Poster presented at the 22nd American Peptide Symposium, American Peptide Society
-
Roodbeen R, Pedersen SL, Jensen KJ. Systematic study of the SPPS of sterically hindered N-methylated peptides using microwave heating. Poster presented at the 22nd American Peptide Symposium, American Peptide Society, 2011.
-
(2011)
-
-
Roodbeen, R.1
Pedersen, S.L.2
Jensen, K.J.3
-
49
-
-
84859126802
-
H-bonding promotion of peptide solubility and cyclization by fluorinated alcohols
-
Hinou H, Hyugaji K, Garcia-Martin F, Nishimura S-I, Albericio F. H-bonding promotion of peptide solubility and cyclization by fluorinated alcohols. RSC Advances, 2012; 2: 2729-2731.
-
(2012)
RSC Advances
, vol.2
, pp. 2729-2731
-
-
Hinou, H.1
Hyugaji, K.2
Garcia-Martin, F.3
Nishimura, S.-I.4
Albericio, F.5
-
50
-
-
84856375207
-
Fast conventional Fmoc solid-phase peptide synthesis: a comparative study of different activators
-
Chantell CA, Onaiyekan MA, Menakuru M. Fast conventional Fmoc solid-phase peptide synthesis: a comparative study of different activators. J. Pept. Sci. 2012; 18: 88-91.
-
(2012)
J. Pept. Sci.
, vol.18
, pp. 88-91
-
-
Chantell, C.A.1
Onaiyekan, M.A.2
Menakuru, M.3
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