205 related articles for article (PubMed ID: 24357151)
1. Evaluation of acid-labile S-protecting groups to prevent Cys racemization in Fmoc solid-phase peptide synthesis.
Hibino H; Miki Y; Nishiuchi Y
J Pept Sci; 2014 Jan; 20(1):30-5. PubMed ID: 24357151
[TBL] [Abstract][Full Text] [Related]
2. 4-Methoxybenzyloxymethyl group, a racemization-resistant protecting group for cysteine in Fmoc solid phase peptide synthesis.
Hibino H; Nishiuchi Y
Org Lett; 2012 Apr; 14(7):1926-9. PubMed ID: 22452360
[TBL] [Abstract][Full Text] [Related]
3. Aqueous microwave-assisted solid-phase peptide synthesis using fmoc strategy. II. Racemization studies and water based synthesis of cysteine-containing peptides.
Hojo K; Shinozaki N; Hara A; Onishi M; Fukumori Y; Ichikawa H
Protein Pept Lett; 2013 Oct; 20(10):1122-8. PubMed ID: 23517723
[TBL] [Abstract][Full Text] [Related]
4. Limiting racemization and aspartimide formation in microwave-enhanced Fmoc solid phase peptide synthesis.
Palasek SA; Cox ZJ; Collins JM
J Pept Sci; 2007 Mar; 13(3):143-8. PubMed ID: 17121420
[TBL] [Abstract][Full Text] [Related]
5. Occurrence and Minimization of Cysteine Racemization during Stepwise Solid-Phase Peptide Synthesis(1)(,)(2).
Han Y; Albericio F; Barany G
J Org Chem; 1997 Jun; 62(13):4307-4312. PubMed ID: 11671751
[TBL] [Abstract][Full Text] [Related]
6. Synthesis and application of Nα-Fmoc-Nπ-4-methoxybenzyloxymethylhistidine in solid phase peptide synthesis.
Hibino H; Miki Y; Nishiuchi Y
J Pept Sci; 2012 Dec; 18(12):763-9. PubMed ID: 23109435
[TBL] [Abstract][Full Text] [Related]
7. Microwave-assisted solid-phase peptide synthesis based on the Fmoc protecting group strategy (CEM).
Vanier GS
Methods Mol Biol; 2013; 1047():235-49. PubMed ID: 23943491
[TBL] [Abstract][Full Text] [Related]
8. Tetrahydropyranyl, a nonaromatic acid-labile Cys protecting group for Fmoc peptide chemistry.
Ramos-Tomillero I; Rodríguez H; Albericio F
Org Lett; 2015 Apr; 17(7):1680-3. PubMed ID: 25764355
[TBL] [Abstract][Full Text] [Related]
9. N-Butylpyrrolidinone for Solid-Phase Peptide Synthesis is Environmentally Friendlier and Synthetically Better than DMF.
Kumar A; Alhassan M; Lopez J; Albericio F; de la Torre BG
ChemSusChem; 2020 Oct; 13(19):5288-5294. PubMed ID: 32720474
[TBL] [Abstract][Full Text] [Related]
10. Aqueous microwave-assisted solid-phase peptide synthesis using Fmoc strategy. III: racemization studies and water-based synthesis of histidine-containing peptides.
Hojo K; Shinozaki N; Hidaka K; Tsuda Y; Fukumori Y; Ichikawa H; Wade JD
Amino Acids; 2014 Oct; 46(10):2347-54. PubMed ID: 24965528
[TBL] [Abstract][Full Text] [Related]
11. Suppressing the epimerization of endothioamide peptides during Fmoc/t-Bu-based solid phase peptide synthesis.
Mukherjee S; Chatterjee J
J Pept Sci; 2016 Nov; 22(11-12):664-672. PubMed ID: 27761972
[TBL] [Abstract][Full Text] [Related]
12. Circular Aqueous Fmoc/t-Bu Solid-Phase Peptide Synthesis.
Pawlas J; Rasmussen JH
ChemSusChem; 2021 Aug; 14(16):3231-3236. PubMed ID: 34270883
[TBL] [Abstract][Full Text] [Related]
13. Deprotection Reagents in Fmoc Solid Phase Peptide Synthesis: Moving Away from Piperidine?
Luna OF; Gomez J; Cárdenas C; Albericio F; Marshall SH; Guzmán F
Molecules; 2016 Nov; 21(11):. PubMed ID: 27854291
[TBL] [Abstract][Full Text] [Related]
14. Aqueous microwave-assisted solid-phase peptide synthesis using Fmoc strategy: in-water synthesis of "difficult sequences".
Hojo K; Ichikawa H; Hara A; Onishi M; Kawasaki K; Fukumori Y
Protein Pept Lett; 2012 Nov; 19(11):1231-6. PubMed ID: 22587785
[TBL] [Abstract][Full Text] [Related]
15. Microwave-assisted cleavage of Alloc and Allyl Ester protecting groups in solid phase peptide synthesis.
Wilson KR; Sedberry S; Pescatore R; Vinton D; Love B; Ballard S; Wham BC; Hutchison SK; Williamson EJ
J Pept Sci; 2016 Oct; 22(10):622-627. PubMed ID: 27501347
[TBL] [Abstract][Full Text] [Related]
16. Advances in Fmoc solid-phase peptide synthesis.
Behrendt R; White P; Offer J
J Pept Sci; 2016 Jan; 22(1):4-27. PubMed ID: 26785684
[TBL] [Abstract][Full Text] [Related]
17. HBTU activation for automated Fmoc solid-phase peptide synthesis.
Fields CG; Lloyd DH; Macdonald RL; Otteson KM; Noble RL
Pept Res; 1991; 4(2):95-101. PubMed ID: 1815783
[TBL] [Abstract][Full Text] [Related]
18. p-Nitrobenzyl side-chain protection for solid-phase synthesis.
Hocker MD; Caldwell CG; Macsata RW; Lyttle MH
Pept Res; 1995; 8(6):310-15. PubMed ID: 8838413
[TBL] [Abstract][Full Text] [Related]
19. Evaluation of unexpected protecting group removal in solid-phase peptide synthesis: Quantified using continuous flow methods.
Laude V; Nuño M; Moses RC; Guthrie D
J Pept Sci; 2022 Dec; 28(12):e3441. PubMed ID: 35785412
[TBL] [Abstract][Full Text] [Related]
20. Incorporation of Fmoc-Dab(Mtt)-OH during solid-phase peptide synthesis: a word of caution.
Lam PL; Wu Y; Wong KL
Org Biomol Chem; 2022 Mar; 20(13):2601-2604. PubMed ID: 35258068
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
