230 related articles for article (PubMed ID: 16957334)
1. Design and synthesis of beta-peptides with biological activity.
Koyack MJ; Cheng RP
Methods Mol Biol; 2006; 340():95-109. PubMed ID: 16957334
[TBL] [Abstract][Full Text] [Related]
2. Solid-phase synthesis of "mixed" peptidomimetics using Fmoc-protected aza-beta3-amino acids and alpha-amino acids.
Busnel O; Bi L; Dali H; Cheguillaume A; Chevance S; Bondon A; Muller S; Baudy-Floc'h M
J Org Chem; 2005 Dec; 70(26):10701-8. PubMed ID: 16355988
[TBL] [Abstract][Full Text] [Related]
3. The world of beta- and gamma-peptides comprised of homologated proteinogenic amino acids and other components.
Seebach D; Beck AK; Bierbaum DJ
Chem Biodivers; 2004 Aug; 1(8):1111-239. PubMed ID: 17191902
[TBL] [Abstract][Full Text] [Related]
4. Aza-amino acid scanning of secondary structure suited for solid-phase peptide synthesis with fmoc chemistry and aza-amino acids with heteroatomic side chains.
Boeglin D; Lubell WD
J Comb Chem; 2005; 7(6):864-78. PubMed ID: 16283795
[TBL] [Abstract][Full Text] [Related]
5. Quaternary β
Yu JS; Noda H; Shibasaki M
Angew Chem Int Ed Engl; 2018 Jan; 57(3):818-822. PubMed ID: 29168280
[TBL] [Abstract][Full Text] [Related]
6. A one-pot procedure for the preparation of N-9-fluorenylmethyloxycarbonyl-α-amino diazoketones from α-amino acids.
Siciliano C; De Marco R; Guidi LE; Spinella M; Liguori A
J Org Chem; 2012 Dec; 77(23):10575-82. PubMed ID: 23146162
[TBL] [Abstract][Full Text] [Related]
7. Synthesis of C-terminal peptide thioesters using Fmoc-based solid-phase peptide chemistry.
Shelton PT; Jensen KJ
Methods Mol Biol; 2013; 1047():119-29. PubMed ID: 23943482
[TBL] [Abstract][Full Text] [Related]
8. Chemical Synthesis of Antimicrobial Peptides.
Münzker L; Oddo A; Hansen PR
Methods Mol Biol; 2017; 1548():35-49. PubMed ID: 28013495
[TBL] [Abstract][Full Text] [Related]
9. Design and synthesis of Fmoc-Thr[PO(OH)(OPOM)] for the preparation of peptide prodrugs containing phosphothreonine in fully protected form.
Qian WJ; Lai CC; Kelley JA; Burke TR
Chem Biodivers; 2014 May; 11(5):784-91. PubMed ID: 24827688
[TBL] [Abstract][Full Text] [Related]
10. Peptidomimetics: Fmoc solid-phase pseudopeptide synthesis.
Cudic P; Stawikowski M
Methods Mol Biol; 2008; 494():223-46. PubMed ID: 18726577
[TBL] [Abstract][Full Text] [Related]
11. Handles for Fmoc solid-phase synthesis of protected peptides.
Góngora-Benítez M; Tulla-Puche J; Albericio F
ACS Comb Sci; 2013 May; 15(5):217-28. PubMed ID: 23573835
[TBL] [Abstract][Full Text] [Related]
12. Solid-phase synthesis of N-nosyl- and N-Fmoc-N-methyl-alpha-amino acids.
Di Gioia ML; Leggio A; Liguori A; Perri F
J Org Chem; 2007 May; 72(10):3723-8. PubMed ID: 17439178
[TBL] [Abstract][Full Text] [Related]
13. Preparation of protected peptidyl thioester intermediates for native chemical ligation by Nalpha-9-fluorenylmethoxycarbonyl (Fmoc) chemistry: considerations of side-chain and backbone anchoring strategies, and compatible protection for N-terminal cysteine.
Gross CM; Lelièvre D; Woodward CK; Barany G
J Pept Res; 2005 Mar; 65(3):395-410. PubMed ID: 15787970
[TBL] [Abstract][Full Text] [Related]
14. Convenient synthesis of N-methylamino acids compatible with Fmoc solid-phase peptide synthesis.
Biron E; Kessler H
J Org Chem; 2005 Jun; 70(13):5183-9. PubMed ID: 15960522
[TBL] [Abstract][Full Text] [Related]
15. Solid-phase guanidinylation of peptidyl amines compatible with standard Fmoc-chemistry: formation of monosubstituted guanidines.
Bionda N; Cudic P
Methods Mol Biol; 2013; 1081():151-65. PubMed ID: 24014439
[TBL] [Abstract][Full Text] [Related]
16. Fmoc Solid-Phase Peptide Synthesis.
Hansen PR; Oddo A
Methods Mol Biol; 2015; 1348():33-50. PubMed ID: 26424261
[TBL] [Abstract][Full Text] [Related]
17. Synthetic strategy for side chain mono-N-alkylation of Fmoc-amino acids promoted by molecular sieves.
Monfregola L; De Luca S
Amino Acids; 2011 Oct; 41(4):981-90. PubMed ID: 21069398
[TBL] [Abstract][Full Text] [Related]
18. Problem of aspartimide formation in Fmoc-based solid-phase peptide synthesis using Dmab group to protect side chain of aspartic acid.
Ruczyński J; Lewandowska B; Mucha P; Rekowski P
J Pept Sci; 2008 Mar; 14(3):335-41. PubMed ID: 17975850
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A new environment-sensitive fluorescent amino acid for Fmoc-based solid phase peptide synthesis.
Eugenio Vazquez M; Rothman DM; Imperiali B
Org Biomol Chem; 2004 Jul; 2(14):1965-6. PubMed ID: 15254619
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]