These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
159 related articles for article (PubMed ID: 32268730)
21. An expanded set of amino acid analogs for the ribosomal translation of unnatural peptides. Hartman MC; Josephson K; Lin CW; Szostak JW PLoS One; 2007 Oct; 2(10):e972. PubMed ID: 17912351 [TBL] [Abstract][Full Text] [Related]
22. Visible-light photoredox synthesis of unnatural chiral α-amino acids. Jiang M; Jin Y; Yang H; Fu H Sci Rep; 2016 May; 6():26161. PubMed ID: 27185220 [TBL] [Abstract][Full Text] [Related]
23. Decarboxylative Side-Chain Functionalization of Aspartic/Glutamic Acids Using Two-Molecule Photoredox Catalysts. Shinkawa Y; Furutani T; Ikeda T; Yamawaki M; Morita T; Yoshimi Y J Org Chem; 2022 Sep; 87(17):11816-11825. PubMed ID: 35952660 [TBL] [Abstract][Full Text] [Related]
24. Radical alkylation of isocyanides with amino acid-/peptide-derived Katritzky salts via photoredox catalysis. Zhu ZF; Zhang MM; Liu F Org Biomol Chem; 2019 Feb; 17(6):1531-1534. PubMed ID: 30681112 [TBL] [Abstract][Full Text] [Related]
26. Visible-Light Photoredox Synthesis of Chiral α-Selenoamino Acids. Jiang M; Yang H; Fu H Org Lett; 2016 May; 18(9):1968-71. PubMed ID: 27093481 [TBL] [Abstract][Full Text] [Related]
27. Bio- and Medicinally Compatible α-Amino-Acid Modification via Merging Photoredox and N-Heterocyclic Carbene Catalysis. Du D; Zhang K; Ma R; Chen L; Gao J; Lu T; Shi Z; Feng J Org Lett; 2020 Aug; 22(16):6370-6375. PubMed ID: 32806184 [TBL] [Abstract][Full Text] [Related]
28. Advances in the synthesis of bioactive unnatural amino acids and peptides. Saladino R; Botta G; Crucianelli M Mini Rev Med Chem; 2012 Apr; 12(4):277-300. PubMed ID: 22303939 [TBL] [Abstract][Full Text] [Related]
29. Rapid and scalable synthesis of innovative unnatural α,β or γ-amino acids functionalized with tertiary amines on their side-chains. Schneider S; Ftouni H; Niu S; Schmitt M; Simonin F; Bihel F Org Biomol Chem; 2015 Jul; 13(25):7020-6. PubMed ID: 26030164 [TBL] [Abstract][Full Text] [Related]
30. Decarboxylative arylation of α-amino acids via photoredox catalysis: a one-step conversion of biomass to drug pharmacophore. Zuo Z; MacMillan DW J Am Chem Soc; 2014 Apr; 136(14):5257-60. PubMed ID: 24712922 [TBL] [Abstract][Full Text] [Related]
31. Catalytic Arylhydroxylation of Dehydroalanine in Continuous Flow for Simple Access to Unnatural Amino Acids. Khan RKM; Zhao Y; Scully TD; Buchwald SL Chemistry; 2018 Oct; 24(57):15215-15218. PubMed ID: 30102444 [TBL] [Abstract][Full Text] [Related]
32. Preparation of modified peptides: direct conversion of α-amino acids into β-amino aldehydes. Saavedra CJ; Boto A; Hernández R Org Biomol Chem; 2012 Jun; 10(22):4448-61. PubMed ID: 22555858 [TBL] [Abstract][Full Text] [Related]
33. A practical and scalable system for heteroaryl amino acid synthesis. Aycock RA; Vogt DB; Jui NT Chem Sci; 2017 Dec; 8(12):7998-8003. PubMed ID: 29619169 [TBL] [Abstract][Full Text] [Related]
34. α-Amino Acids and Peptides as Bifunctional Reagents: Carbocarboxylation of Activated Alkenes via Recycling CO Liao LL; Cao GM; Jiang YX; Jin XH; Hu XL; Chruma JJ; Sun GQ; Gui YY; Yu DG J Am Chem Soc; 2021 Feb; 143(7):2812-2821. PubMed ID: 33561344 [TBL] [Abstract][Full Text] [Related]
35. Decarboxylative Peptide Macrocyclization through Photoredox Catalysis. McCarver SJ; Qiao JX; Carpenter J; Borzilleri RM; Poss MA; Eastgate MD; Miller MM; MacMillan DW Angew Chem Int Ed Engl; 2017 Jan; 56(3):728-732. PubMed ID: 27860140 [TBL] [Abstract][Full Text] [Related]
36. Some of the amino acid chemistry going on in the Laboratory of Amino Acids, Peptides and Proteins. Bouifraden S; Drouot C; el Hadrami M; Guenoun F; Lecointe L; Mai N; Paris M; Pothion C; Sadoune M; Sauvagnat B; Amblard M; Aubagnac JL; Calmes M; Chevallet P; Daunis J; Enjalbal C; Fehrentz JA; Lamaty F; Lavergne JP; Lazaro R; Rolland V; Roumestant ML; Viallefont P; Vidal Y; Martinez J Amino Acids; 1999; 16(3-4):345-79. PubMed ID: 10399020 [TBL] [Abstract][Full Text] [Related]