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- Double stereodifferentiation in aldol reactions of pyroglutamic urethane esters1. Bernard A. Starkmann, Douglas W. Young
, J. Chem. Soc., Perkin Trans. 1
, 2002
, 725
- Biofixation of a high-concentration of carbon dioxide using a deep-sea bacterium: Sulfurovum lithotrophicum 42BKTT. Hyuk-Sung Kwon, Jae-Hyuk Lee, Taekyung Kim, Jae-Jeong Kim, Philip Jeon, Chang-Ha Lee, Ik-Sung Ahn
, RSC Adv.
, 2015
, 5
, 7151
- Two separate and distinct syntheses of stereospecifically deuteriated samples of (2S)-proline. Paul Barraclough, Petra Dieterich, Caroline A. Spray, Douglas W. Young
, Org. Biomol. Chem.
, 2006
, 4
, 1483
- Structural comparison of two anti-CD20 monoclonal antibody drug products using middle-down mass spectrometry. Bo Wang, Ashley C. Gucinski, David A. Keire, Lucinda F. Buhse, Michael T. Boyne II
, Analyst
, 2013
, 138
, 3058
- Pyroglutamate-modified amyloid β(3–42) monomer has more β-sheet content than the amyloid β(1–42) monomer. Soumav Nath, Alexander K. Buell, Bogdan Barz
, Phys. Chem. Chem. Phys.
, 2023
, 25
, 16483
- Metabolomic identification of novel biomarkers of nasopharyngeal carcinoma. Lunzhao Yi, Naiping Dong, Shuting Shi, Baichuan Deng, Yonghuan Yun, Zhibiao Yi, Yi Zhang
, RSC Adv.
, 2014
, 4
, 59094
- Plant peptides – redefining an area of ribosomally synthesized and post-translationally modified peptides. Jonathan R. Chekan, Lisa S. Mydy, Michael A. Pasquale, Roland D. Kersten
, Nat. Prod. Rep.
, 2024
- Structural characteristics of oligomers formed by pyroglutamate-modified amyloid β peptides studied by solid-state NMR. Holger A. Scheidt, Anirban Das, Alexander Korn, Martin Krueger, Sudipta Maiti, Daniel Huster
, Phys. Chem. Chem. Phys.
, 2020
, 22
, 16887
- Synthesis of homochiral amino acid pyrazine and pyrrole analogues of glutamate
antagonists. Andrew Dinsmore, Paul M. Doyle, Matthias Steger, Douglas W. Young
, J. Chem. Soc., Perkin Trans. 1
, 2002
, 613
- Use of a modified ring-switching strategy to synthesise the glutamate antagonist (2S)-2-amino-3-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)propionate and related compounds with two chiral centres1. Andrew Dinsmore, Paul M. Doyle, Douglas W. Young
, J. Chem. Soc., Perkin Trans. 1
, 2002
, 155