343 related articles for article (PubMed ID: 22920411)
21. Microwave-assisted solid-phase peptide synthesis of the 60-110 domain of human pleiotrophin on 2-chlorotrityl resin.
Friligou I; Papadimitriou E; Gatos D; Matsoukas J; Tselios T
Amino Acids; 2011 May; 40(5):1431-40. PubMed ID: 20872260
[TBL] [Abstract][Full Text] [Related]
22. Immobilized coupling reagents: synthesis of amides/peptides.
Cherkupally P; Ramesh S; de la Torre BG; Govender T; Kruger HG; Albericio F
ACS Comb Sci; 2014 Nov; 16(11):579-601. PubMed ID: 25330282
[TBL] [Abstract][Full Text] [Related]
23. A Dde resin based strategy for inverse solid-phase synthesis of amino terminated peptides, peptide mimetics and protected peptide intermediates.
Rai A; Gutheil WG
J Pept Sci; 2005 Feb; 11(2):69-73. PubMed ID: 15635629
[TBL] [Abstract][Full Text] [Related]
24. Microwave-assisted Boc-solid phase peptide synthesis of cyclic cysteine-rich peptides.
Cemazar M; Craik DJ
J Pept Sci; 2008 Jun; 14(6):683-9. PubMed ID: 18044816
[TBL] [Abstract][Full Text] [Related]
25. Phosphoramidate-peptide synthesis by solution- and solid-phase Staudinger-phosphite reactions.
Serwa RA; Swiecicki JM; Homann D; Hackenberger CP
J Pept Sci; 2010 Oct; 16(10):563-7. PubMed ID: 20862723
[TBL] [Abstract][Full Text] [Related]
26. New TFA-free cleavage and final deprotection in fmoc solid-phase peptide synthesis: dilute HCl in fluoro alcohol.
Palladino P; Stetsenko DA
Org Lett; 2012 Dec; 14(24):6346-9. PubMed ID: 23210918
[TBL] [Abstract][Full Text] [Related]
27. Tag-assisted liquid-phase peptide synthesis using hydrophobic benzyl alcohols as supports.
Okada Y; Suzuki H; Nakae T; Fujita S; Abe H; Nagano K; Yamada T; Ebata N; Kim S; Chiba K
J Org Chem; 2013 Jan; 78(2):320-7. PubMed ID: 23215232
[TBL] [Abstract][Full Text] [Related]
28. N-methyl-phenacyloxycarbamidomethyl (Pocam) group: a novel thiol protecting group for solid-phase peptide synthesis and peptide condensation reactions.
Katayama H; Nakahara Y; Hojo H
Org Biomol Chem; 2011 Jun; 9(12):4653-61. PubMed ID: 21537511
[TBL] [Abstract][Full Text] [Related]
29. Depsipeptide methodology for solid-phase peptide synthesis: circumventing side reactions and development of an automated technique via depsidipeptide units.
Coin I; Dölling R; Krause E; Bienert M; Beyermann M; Sferdean CD; Carpino LA
J Org Chem; 2006 Aug; 71(16):6171-7. PubMed ID: 16872202
[TBL] [Abstract][Full Text] [Related]
30. Solid-phase synthesis of diverse peptide tertiary amides by reductive amination.
Pels K; Kodadek T
ACS Comb Sci; 2015 Mar; 17(3):152-5. PubMed ID: 25695359
[TBL] [Abstract][Full Text] [Related]
31. Native chemical ligation derived method for recombinant peptide/protein C-terminal amidation.
Sun C; Luo G; Neravetla S; Ghosh SS; Forood B
Bioorg Med Chem Lett; 2013 Sep; 23(18):5203-8. PubMed ID: 23880540
[TBL] [Abstract][Full Text] [Related]
32. Peptide synthesis 'in water' by a solution-phase method using water-dispersible nanoparticle Boc-amino acid.
Hojo K; Ichikawa H; Onishi M; Fukumori Y; Kawasaki K
J Pept Sci; 2011 Jul; 17(7):487-92. PubMed ID: 21495120
[TBL] [Abstract][Full Text] [Related]
33. Trimethoxyphenylthio as a highly labile replacement for tert-butylthio cysteine protection in Fmoc solid phase synthesis.
Postma TM; Giraud M; Albericio F
Org Lett; 2012 Nov; 14(21):5468-71. PubMed ID: 23075145
[TBL] [Abstract][Full Text] [Related]
34. A dimethyl ketal-protected benzoin-based linker suitable for photolytic release of unprotected peptides.
Chumachenko N; Novikov Y; Shoemaker RK; Copley SD
J Org Chem; 2011 Nov; 76(22):9409-16. PubMed ID: 21950361
[TBL] [Abstract][Full Text] [Related]
35. The phenacyl group as an efficient thiol protecting group in a peptide condensation reaction by the thioester method.
Katayama H; Hojo H
Org Biomol Chem; 2013 Jul; 11(26):4405-13. PubMed ID: 23715434
[TBL] [Abstract][Full Text] [Related]
36. Use of trichloroacetimidate linker in solid-phase Peptide synthesis.
Yan LZ; Mayer JP
J Org Chem; 2003 Feb; 68(3):1161-2. PubMed ID: 12558452
[TBL] [Abstract][Full Text] [Related]
37. Facile solid-phase synthesis of C-terminal peptide aldehydes and hydroxamates from a common Backbone Amide-Linked (BAL) intermediate.
Gazal S; Masterson LR; Barany G
J Pept Res; 2005 Dec; 66(6):324-32. PubMed ID: 16316448
[TBL] [Abstract][Full Text] [Related]
38. Thiophene backbone amide linkers, a new class of easily prepared and highly acid-labile linkers for solid-phase synthesis.
Jessing M; Brandt M; Jensen KJ; Christensen JB; Boas U
J Org Chem; 2006 Sep; 71(18):6734-41. PubMed ID: 16930022
[TBL] [Abstract][Full Text] [Related]
39. A new water-soluble N-protecting group, 2-(phenyl(methyl)sulfonio)ethyloxycarbonyl tetrafluoroborate, and its application to solid phase peptide synthesis in water.
Hojo K; Maeda M; Kawasaki K
J Pept Sci; 2001 Dec; 7(12):615-8. PubMed ID: 11798017
[TBL] [Abstract][Full Text] [Related]
40. Emerging methods in amide- and peptide-bond formation.
Bode JW
Curr Opin Drug Discov Devel; 2006 Nov; 9(6):765-75. PubMed ID: 17117685
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
