255 related articles for article (PubMed ID: 23075145)
1. 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]
2. Efficient preparation of Fmoc-aminoacyl-N-ethylcysteine unit, a key device for the synthesis of peptide thioesters.
Hojo H; Kobayashi H; Ubagai R; Asahina Y; Nakahara Y; Katayama H; Ito Y; Nakahara Y
Org Biomol Chem; 2011 Oct; 9(19):6807-13. PubMed ID: 21842100
[TBL] [Abstract][Full Text] [Related]
3. Automated Fmoc-based solid-phase synthesis of peptide thioesters with self-purification effect and application in the construction of immobilized SH3 domains.
Mende F; Beisswenger M; Seitz O
J Am Chem Soc; 2010 Aug; 132(32):11110-8. PubMed ID: 20662535
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 2-nitroveratryl as a photocleavable thiol-protecting group for directed disulfide bond formation in the chemical synthesis of insulin.
Karas JA; Scanlon DB; Forbes BE; Vetter I; Lewis RJ; Gardiner J; Separovic F; Wade JD; Hossain MA
Chemistry; 2014 Jul; 20(31):9549-52. PubMed ID: 24957739
[TBL] [Abstract][Full Text] [Related]
6. Synthesis and pharmacology of novel analogues of oxytocin and deaminooxytocin: directed methods for the construction of disulfide and trisulfide bridges in peptides.
Chen L; Zoulíková I; Slaninová J; Barany G
J Med Chem; 1997 Mar; 40(6):864-76. PubMed ID: 9083475
[TBL] [Abstract][Full Text] [Related]
7. Regioselective formation of multiple disulfide bonds with the aid of postsynthetic S-tritylation.
Mochizuki M; Tsuda S; Tanimura K; Nishiuchi Y
Org Lett; 2015 May; 17(9):2202-5. PubMed ID: 25860514
[TBL] [Abstract][Full Text] [Related]
8. Pyroacm Resin: An Acetamidomethyl Derived Resin for Solid Phase Synthesis of Peptides through Side Chain Anchoring of C-Terminal Cysteine Residues.
Juvekar V; Gong YD
Org Lett; 2016 Feb; 18(4):836-9. PubMed ID: 26845647
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Side-chain anchoring strategy for solid-phase synthesis of peptide acids with C-terminal cysteine.
Barany G; Han Y; Hargittai B; Liu RQ; Varkey JT
Biopolymers; 2003; 71(6):652-66. PubMed ID: 14991675
[TBL] [Abstract][Full Text] [Related]
11. Optimized Fmoc solid-phase synthesis of the cysteine-rich peptide linaclotide.
Góngora-Benítez M; Tulla-Puche J; Paradís-Bas M; Werbitzky O; Giraud M; Albericio F
Biopolymers; 2011; 96(1):69-80. PubMed ID: 20560145
[TBL] [Abstract][Full Text] [Related]
12. Bis(2-sulfanylethyl)amino native peptide ligation.
Ollivier N; Dheur J; Mhidia R; Blanpain A; Melnyk O
Org Lett; 2010 Nov; 12(22):5238-41. PubMed ID: 20964289
[TBL] [Abstract][Full Text] [Related]
13. A rapid and efficient method for the synthesis of selectively S-Trt or S-Mmt protected Cys-containing peptides.
Stathopoulos P; Papas S; Sakka M; Tzakos AG; Tsikaris V
Amino Acids; 2014 May; 46(5):1367-76. PubMed ID: 24609270
[TBL] [Abstract][Full Text] [Related]
14. Access to cyclic or branched peptides using bis(2-sulfanylethyl)amido side-chain derivatives of Asp and Glu.
Boll E; Dheur J; Drobecq H; Melnyk O
Org Lett; 2012 May; 14(9):2222-5. PubMed ID: 22537053
[TBL] [Abstract][Full Text] [Related]
15. Redox-active bis-cysteinyl peptides. I. Synthesis of cyclic cystinyl peptides by conventional methods in solution and on solid supports.
Musiol HJ; Siedler F; Quarzago D; Moroder L
Biopolymers; 1994 Nov; 34(11):1553-62. PubMed ID: 7827266
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Preparation and use of cysteine orthoesters for solid-supported synthesis of peptides.
Huang Z; Derksen DJ; Vederas JC
Org Lett; 2010 May; 12(10):2282-5. PubMed ID: 20405951
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 2,2'-Dithiobis(5-nitropyridine) (DTNP) as an effective and gentle deprotectant for common cysteine protecting groups.
Schroll AL; Hondal RJ; Flemer S
J Pept Sci; 2012 Jan; 18(1):1-9. PubMed ID: 22083608
[TBL] [Abstract][Full Text] [Related]
20. Acid-catalyzed tandem thiol switch for preparing peptide thioesters from mercaptoethyl esters.
Eom KD; Tam JP
Org Lett; 2011 May; 13(10):2610-3. PubMed ID: 21517126
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
