343 related articles for article (PubMed ID: 22920411)
1. Novel diphenylmethyl-derived amide protecting group for efficient liquid-phase peptide synthesis: AJIPHASE.
Takahashi D; Yano T; Fukui T
Org Lett; 2012 Sep; 14(17):4514-7. PubMed ID: 22920411
[TBL] [Abstract][Full Text] [Related]
2. Solid phase synthesis of C-terminal peptide amides: development of a new aminoethyl-polystyrene linker on the Multipin solid support.
Bui CT; Bray AM; Nguyen T; Ercole F; Maeji NJ
J Pept Sci; 2000 May; 6(5):243-50. PubMed ID: 10823493
[TBL] [Abstract][Full Text] [Related]
3. SPPS of protected peptidyl aminoalkyl amides.
Karavoltsos M; Mourtas S; Gatos D; Barlos K
J Pept Sci; 2002 Nov; 8(11):615-20. PubMed ID: 12487429
[TBL] [Abstract][Full Text] [Related]
4. Backbone amide linker strategies for the solid-phase synthesis of C-terminal modified peptides.
Alsina J; Kates SA; Barany G; Albericio F
Methods Mol Biol; 2005; 298():195-208. PubMed ID: 16044548
[TBL] [Abstract][Full Text] [Related]
5. Synthesis and comparative properties of two amide-generating resin linkers for use in solid phase peptide synthesis.
Deng FK; Mandal K; Luisier S; Kent SB
J Pept Sci; 2010 Oct; 16(10):545-50. PubMed ID: 20824627
[TBL] [Abstract][Full Text] [Related]
6. Microwave-assisted synthesis of difficult sequence-containing peptides using the isopeptide method.
Hussein WM; Liu TY; Toth I; Skwarczynski M
Org Biomol Chem; 2013 Apr; 11(14):2370-6. PubMed ID: 23429456
[TBL] [Abstract][Full Text] [Related]
7. C-terminal N-alkylated peptide amides resulting from the linker decomposition of the Rink amide resin: a new cleavage mixture prevents their formation.
Stathopoulos P; Papas S; Tsikaris V
J Pept Sci; 2006 Mar; 12(3):227-32. PubMed ID: 16103992
[TBL] [Abstract][Full Text] [Related]
8. Linkers, resins, and general procedures for solid-phase peptide synthesis.
Shelton PT; Jensen KJ
Methods Mol Biol; 2013; 1047():23-41. PubMed ID: 23943476
[TBL] [Abstract][Full Text] [Related]
9. AJIPHASE®: A Highly Efficient Synthetic Method for One-Pot Peptide Elongation in the Solution Phase by an Fmoc Strategy.
Takahashi D; Inomata T; Fukui T
Angew Chem Int Ed Engl; 2017 Jun; 56(27):7803-7807. PubMed ID: 28504858
[TBL] [Abstract][Full Text] [Related]
10. Ethyl 2-cyano-2-(2-nitrobenzenesulfonyloxyimino)acetate (o-NosylOXY): a recyclable coupling reagent for racemization-free synthesis of peptide, amide, hydroxamate, and ester.
Dev D; Palakurthy NB; Thalluri K; Chandra J; Mandal B
J Org Chem; 2014 Jun; 79(12):5420-31. PubMed ID: 24849944
[TBL] [Abstract][Full Text] [Related]
11. Solid-phase peptide synthesis using nanoparticulate amino acids in water.
Hojo K; Ichikawa H; Maeda M; Kida S; Fukumori Y; Kawasaki K
J Pept Sci; 2007 Jul; 13(7):493-7. PubMed ID: 17554805
[TBL] [Abstract][Full Text] [Related]
12. Backbone amide linker strategy: protocols for the synthesis of C-terminal peptide aldehydes.
Shelton PT; Jensen KJ
Methods Mol Biol; 2013; 1047():131-9. PubMed ID: 23943483
[TBL] [Abstract][Full Text] [Related]
13. Two dialkoxynaphthalene aldehydes as backbone amide linkers for solid-phase synthesis.
Boas U; Christensen JB; Jensen KJ
J Comb Chem; 2004; 6(4):497-503. PubMed ID: 15244410
[TBL] [Abstract][Full Text] [Related]
14. O-N intramolecular acyl migration reaction in the development of prodrugs and the synthesis of difficult sequence-containing bioactive peptides.
Sohma Y; Hayashi Y; Skwarczynski M; Hamada Y; Sasaki M; Kimura T; Kiso Y
Biopolymers; 2004; 76(4):344-56. PubMed ID: 15386265
[TBL] [Abstract][Full Text] [Related]
15. Oligonucleotides with 2'-O-carboxymethyl group: synthesis and 2'-conjugation via amide bond formation on solid phase.
Kachalova A; Zubin E; Stetsenko D; Gait M; Oretskaya T
Org Biomol Chem; 2004 Oct; 2(19):2793-7. PubMed ID: 15455151
[TBL] [Abstract][Full Text] [Related]
16. Solid-phase peptide synthesis (SPPS), C-terminal vs. side-chain anchoring: a reality or a myth.
Cherkupally P; Acosta GA; Ramesh S; De la Torre BG; Govender T; Kruger HG; Albericio F
Amino Acids; 2014 Aug; 46(8):1827-38. PubMed ID: 24770904
[TBL] [Abstract][Full Text] [Related]
17. Backbone amide linker (BAL) strategy for Nalpha-9-fluorenylmethoxycarbonyl (Fmoc) solid-phase synthesis of peptide aldehydes.
Kappel JC; Barany G
J Pept Sci; 2005 Sep; 11(9):525-35. PubMed ID: 16001455
[TBL] [Abstract][Full Text] [Related]
18. Synthesis of 'head-to-tail' cyclized peptides on solid support using a chelating amide as new orthogonal protecting group.
Lay M; Bannwarth W
J Pept Sci; 2015 Jun; 21(6):461-6. PubMed ID: 25754861
[TBL] [Abstract][Full Text] [Related]
19. Benzhydrylamine linker grafting: a strategy for the improved synthesis of C-terminal peptide amides.
Alewood D; Hopping G; Brust A; Reid RC; Alewood PF
J Pept Sci; 2010 Oct; 16(10):551-7. PubMed ID: 20862722
[TBL] [Abstract][Full Text] [Related]
20. 2-Methoxy-4-methylsulfinylbenzyl: a backbone amide safety-catch protecting group for the synthesis and purification of difficult peptide sequences.
Paradís-Bas M; Tulla-Puche J; Albericio F
Chemistry; 2014 Nov; 20(46):15031-9. PubMed ID: 25280354
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]