225 related articles for article (PubMed ID: 20225219)
1. Efficient synthesis of Fmoc-protected phosphinic pseudodipeptides: Building blocks for the synthesis of matrix metalloproteinase inhibitors.
Bhowmick M; Sappidi RR; Fields GB; Lepore SD
Biopolymers; 2011; 96(1):1-3. PubMed ID: 20225219
[TBL] [Abstract][Full Text] [Related]
2. Synthesis of Fmoc-Gly-Ile Phosphinic Pseudodipeptide: Residue Specific Conditions for Construction of Matrix Metalloproteinase Inhibitor Building Blocks.
Bhowmick M; Fields GB
Int J Pept Res Ther; 2012 Dec; 18(4):335-339. PubMed ID: 24496015
[TBL] [Abstract][Full Text] [Related]
3. Synthesis of α-carboxyphosphinopeptides derived from norleucine.
Pícha J; Buděšínský M; Fiedler P; Sanda M; Jiráček J
Amino Acids; 2010 Nov; 39(5):1265-80. PubMed ID: 20349321
[TBL] [Abstract][Full Text] [Related]
4. Shortcut to fmoc-protected phosphinic pseudodipeptidic blocks.
Matziari M; Yiotakis A
Org Lett; 2005 Sep; 7(18):4049-52. PubMed ID: 16119964
[TBL] [Abstract][Full Text] [Related]
5. A versatile annulation protocol toward novel constrained phosphinic peptidomimetics.
Nasopoulou M; Georgiadis D; Matziari M; Dive V; Yiotakis A
J Org Chem; 2007 Sep; 72(19):7222-8. PubMed ID: 17715974
[TBL] [Abstract][Full Text] [Related]
6. An efficient and highly selective deprotection of N-Fmoc-alpha-amino acid and lipophilic N-Fmoc-dipeptide methyl esters with aluminium trichloride and N,N-dimethylaniline.
Di Gioia ML; Leggio A; Le Pera A; Siciliano C; Liguori A; Sindona G
J Pept Res; 2004 Apr; 63(4):383-7. PubMed ID: 15102056
[TBL] [Abstract][Full Text] [Related]
7. A synthetic method for diversification of the P1' substituent in phosphinic dipeptides as a tool for exploration of the specificity of the S1' binding pockets of leucine aminopeptidases.
Vassiliou S; Xeilari M; Yiotakis A; Grembecka J; Pawełczak M; Kafarski P; Mucha A
Bioorg Med Chem; 2007 May; 15(9):3187-200. PubMed ID: 17337192
[TBL] [Abstract][Full Text] [Related]
8. Application of in situ silylation for improved, convenient preparation of fluorenylmethoxycarbonyl (Fmoc)-protected phosphinate amino acids.
Li S; Whitehead JK; Hammer RP
J Org Chem; 2007 Apr; 72(8):3116-8. PubMed ID: 17375960
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Individual stereoisomers of phosphinic dipeptide inhibitor of leucine aminopeptidase.
Mucha A; Lämmerhofer M; Lindner W; Pawełczak M; Kafarski P
Bioorg Med Chem Lett; 2008 Mar; 18(5):1550-4. PubMed ID: 18262419
[TBL] [Abstract][Full Text] [Related]
11. Convenient synthesis and diversification of dehydroalaninyl phosphinic peptide analogues.
Matziari M; Georgiadis D; Dive V; Yiotakis A
Org Lett; 2001 Mar; 3(5):659-62. PubMed ID: 11259030
[TBL] [Abstract][Full Text] [Related]
12. Characterization of Nα-Fmoc-protected dipeptide isomers by electrospray ionization tandem mass spectrometry (ESI-MS(n)): effect of protecting group on fragmentation of dipeptides.
Ramesh M; Raju B; Srinivas R; Sureshbabu VV; Vishwanatha TM; Hemantha HP
Rapid Commun Mass Spectrom; 2011 Jul; 25(14):1949-58. PubMed ID: 21698678
[TBL] [Abstract][Full Text] [Related]
13. Synthesis of N-carboxyalkyl and N-aminoalkyl functionalized dipeptide building units for the assembly of backbone cyclic peptides.
Müller B; Besser D; Kleinwächter P; Arad O; Reissmann S
J Pept Res; 1999 Nov; 54(5):383-93. PubMed ID: 10563504
[TBL] [Abstract][Full Text] [Related]
14. Diastereoselective synthesis of alpha,beta'-disubstituted aminomethyl(2-carboxyethyl)phosphinates as phosphinyl dipeptide isosteres.
Yamagishi T; Ichikawa H; Haruki T; Yokomatsu T
Org Lett; 2008 Oct; 10(19):4347-50. PubMed ID: 18781768
[TBL] [Abstract][Full Text] [Related]
15. Preventing aspartimide formation in Fmoc SPPS of Asp-Gly containing peptides--practical aspects of new trialkylcarbinol based protecting groups.
Behrendt R; Huber S; White P
J Pept Sci; 2016 Feb; 22(2):92-7. PubMed ID: 26751703
[TBL] [Abstract][Full Text] [Related]
16. Solid-phase synthesis of phosphinic dipepetide isosteres and beta amino acids via activated N-terminal acrylamides.
Manzenrieder F; Kessler H
Adv Exp Med Biol; 2009; 611():11-2. PubMed ID: 19400072
[No Abstract] [Full Text] [Related]
17. Synthesis of differentially protected N-acylated reduced pseudodipeptides as building units for backbone cyclic peptides.
Besser D; Müller B; Agricola I; Reissmann S
J Pept Sci; 2000 Mar; 6(3):130-8. PubMed ID: 10759211
[TBL] [Abstract][Full Text] [Related]
18. Design, synthesis, and metal binding of novel Pseudo- oligopeptides containing two phosphinic acid groups.
Ye Y; Liu M; Kao JL; Marshall GR
Biopolymers; 2008 Jan; 89(1):72-85. PubMed ID: 17910046
[TBL] [Abstract][Full Text] [Related]
19. Chemoselective protection of solid-phase compatible Fmoc-phosphinic building blocks.
Nasopoulou M; Matziari M; Dive V; Yiotakis A
J Org Chem; 2006 Dec; 71(25):9525-7. PubMed ID: 17137389
[TBL] [Abstract][Full Text] [Related]
20. Fmoc-based solid-phase synthesis of GPR54-agonistic pentapeptide derivatives containing alkene- and fluoroalkene-dipeptide isosteres.
Tomita K; Narumi T; Niida A; Oishi S; Ohno H; Fujii N
Biopolymers; 2007; 88(2):272-8. PubMed ID: 17216632
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
