321 related articles for article (PubMed ID: 12054934)
1. Homochiral 4-azalysine building blocks: syntheses and applications in solid-phase chemistry.
Chhabra SR; Mahajan A; Chan WC
J Org Chem; 2002 Jun; 67(12):4017-29. PubMed ID: 12054934
[TBL] [Abstract][Full Text] [Related]
2. Solid-phase route to Fmoc-protected cationic amino acid building blocks.
Clausen JD; Linderoth L; Nielsen HM; Franzyk H
Amino Acids; 2012 Oct; 43(4):1633-41. PubMed ID: 22358257
[TBL] [Abstract][Full Text] [Related]
3. Facile synthesis of orthogonally protected amino acid building blocks for combinatorial N-backbone cyclic peptide chemistry.
Gellerman G; Elgavi A; Salitra Y; Kramer M
J Pept Res; 2001 Apr; 57(4):277-91. PubMed ID: 11328485
[TBL] [Abstract][Full Text] [Related]
4. Highly efficient and enantioselective syntheses of (2S,3R)-3-alkyl- and alkenylglutamates from Fmoc-protected Garner's aldehyde.
Moreira R; Taylor SD
Amino Acids; 2020 Jul; 52(6-7):987-998. PubMed ID: 32621203
[TBL] [Abstract][Full Text] [Related]
5. A concise methodology for the stereoselective synthesis of O-glycosylated amino acid building blocks: complete 1H NMR assignments and their application in solid-phase glycopeptide synthesis.
Satyanarayana J; Gururaja TL; Naganagowda GA; Ramasubbu N; Levine MJ
J Pept Res; 1998 Sep; 52(3):165-79. PubMed ID: 9774229
[TBL] [Abstract][Full Text] [Related]
6. Development of orthogonally protected hypusine for solid-phase peptide synthesis.
Song A; Tom J; Yu Z; Pham V; Tan D; Zhang D; Fang G; Yu T; Deshayes K
J Org Chem; 2015 Apr; 80(7):3677-81. PubMed ID: 25769022
[TBL] [Abstract][Full Text] [Related]
7. Improved Synthesis of the Unnatural Amino Acids AHMOD and AMD, Components of the Anticancer Peptaibol Culicinin D.
Ko KY; Wagner S; Yang SH; Furkert DP; Brimble MA
J Org Chem; 2015 Sep; 80(17):8631-6. PubMed ID: 26252224
[TBL] [Abstract][Full Text] [Related]
8. Extensively stereodiversified scaffolds for use in diversity-oriented library synthesis.
Gierasch TM; Shi Z; Verdine GL
Org Lett; 2003 Mar; 5(5):621-4. PubMed ID: 12605474
[TBL] [Abstract][Full Text] [Related]
9. Diversity-oriented synthesis of azapeptides with basic amino acid residues: aza-lysine, aza-ornithine, and aza-arginine.
Traoré M; Doan ND; Lubell WD
Org Lett; 2014 Jul; 16(13):3588-91. PubMed ID: 24959890
[TBL] [Abstract][Full Text] [Related]
10. Solid-phase synthesis of a tyrphostin ether library.
Guo G; Arvanitis EA; Pottorf RS; Player MR
J Comb Chem; 2003; 5(4):408-13. PubMed ID: 12857109
[TBL] [Abstract][Full Text] [Related]
11. Exploring side-chain diversity by submonomer solid-phase aza-peptide synthesis.
Sabatino D; Proulx C; Klocek S; Bourguet CB; Boeglin D; Ong H; Lubell WD
Org Lett; 2009 Aug; 11(16):3650-3. PubMed ID: 19606817
[TBL] [Abstract][Full Text] [Related]
12. Solid-phase synthesis of chiral 3,4-diazaphospholanes and their application to catalytic asymmetric allylic alkylation.
Landis CR; Clark TP
Proc Natl Acad Sci U S A; 2004 Apr; 101(15):5428-32. PubMed ID: 14985503
[TBL] [Abstract][Full Text] [Related]
13. Synthesis of cyclic peptidomimetics from aldol building blocks.
Sasmal S; Geyer A; Maier ME
J Org Chem; 2002 Aug; 67(17):6260-3. PubMed ID: 12182676
[TBL] [Abstract][Full Text] [Related]
14. Large-pore polydimethylacrylamide resin for solid-phase peptide synthesis: applications in Fmoc chemistry.
Sparrow JT; Knieb-Cordonier NG; Obeyseskere NU; McMurray JS
Pept Res; 1996; 9(6):297-304. PubMed ID: 9048423
[TBL] [Abstract][Full Text] [Related]
15. Efficient solid-phase synthesis of peptide-based phosphine ligands: towards combinatorial libraries of selective transition metal catalysts.
Christensen CA; Meldal M
Chemistry; 2005 Jul; 11(14):4121-31. PubMed ID: 15861474
[TBL] [Abstract][Full Text] [Related]
16. Annulation of primary amines to piperazines and diazaspirocycles utilizing alpha-methyl benzyl resin.
Macleod C; Martinez-Teipel BI; Barker WM; Dolle RE
J Comb Chem; 2006; 8(1):132-40. PubMed ID: 16398564
[TBL] [Abstract][Full Text] [Related]
17. Orthogonally protected artificial amino acid as tripod ligand for automated peptide synthesis and labeling with [(99m)Tc(OH(2))(3)(CO)(3)](+).
Shen Y; Schottelius M; Zelenka K; De Simone M; Pohle K; Kessler H; Wester HJ; Schmutz P; Alberto R
Bioconjug Chem; 2013 Jan; 24(1):26-35. PubMed ID: 23237229
[TBL] [Abstract][Full Text] [Related]
18. Efficient Building Blocks for Solid-Phase Peptide Synthesis of Spin Labeled Peptides for Electron Paramagnetic Resonance and Dynamic Nuclear Polarization Applications.
Brodrecht M; Herr K; Bothe S; de Oliveira M; Gutmann T; Buntkowsky G
Chemphyschem; 2019 Jun; 20(11):1475-1487. PubMed ID: 30950574
[TBL] [Abstract][Full Text] [Related]
19. Synthesis of novel unnatural amino acid as a building block and its incorporation into an antimicrobial peptide.
Oh JE; Lee KH
Bioorg Med Chem; 1999 Dec; 7(12):2985-90. PubMed ID: 10658605
[TBL] [Abstract][Full Text] [Related]
20. Asymmetric trienamine catalysis for the construction of structurally rigid cyclic α,α-disubstituted amino acid derivatives.
Jiang H; Gschwend B; Albrecht Ł; Hansen SG; Jørgensen KA
Chemistry; 2011 Aug; 17(33):9032-6. PubMed ID: 21744409
[No Abstract] [Full Text] [Related]
[Next] [New Search]
