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- Exploring the solid state phase transition in dl-norvaline with terahertz spectroscopy. Jens Neu, Coleen T. Nemes, Kevin P. Regan, Michael R. C. Williams, Charles A. Schmuttenmaer
, Phys. Chem. Chem. Phys.
, 2018
, 20
, 276
- Structure-guided engineering of meso-diaminopimelate dehydrogenase for enantioselective reductive amination of sterically bulky 2-keto acids. Xinkuan Cheng, Xi Chen, Jinhui Feng, Qiaqing Wu, Dunming Zhu
, Catal. Sci. Technol.
, 2018
, 8
, 4994
- 35. The 4-hydroxypipecolic acid from acacia species, and its stereoisomers. J. W. Clark-Lewis, P. I. Mortimer
, J. Chem. Soc.
, 1961
, 189
- Formation and structure of the ferryl [FeO] intermediate in the non-haem iron halogenase SyrB2: classical and QM/MM modelling agree. G. Rugg, H. M. Senn
, Phys. Chem. Chem. Phys.
, 2017
, 19
, 30107
- Side chain homologation of alanyl peptide nucleic acids: pairing selectivity and stacking. Ulf Diederichsen, Daniel Weicherding, Nicola Diezemann
, Org. Biomol. Chem.
, 2005
, 3
, 1058
- Polymorphism of the quasiracemate d-2-aminobutyric acid:l-norvaline. M. M. H. Smets, E. Kalkman, P. Tinnemans, A. M. Krieger, H. Meekes, H. M. Cuppen
, CrystEngComm
, 2017
, 19
, 5604
- Dual photothermal MDSCs-targeted immunotherapy inhibits lung immunosuppressive metastasis by enhancing T-cell recruitment. Kalliopi Domvri, Savvas Petanidis, Doxakis Anestakis, Konstantinos Porpodis, Chong Bai, Paul Zarogoulidis, Lutz Freitag, Wolfgang Hohenforst-Schmidt, Theodora Katopodi
, Nanoscale
, 2020
, 12
, 7051
- Substrate-product analogue inhibitors of isoleucine 2-epimerase from Lactobacillus buchneri by rational design. Noa T. Sorbara, Joshua W. M. MacMillan, Gregory D. McCluskey, Stephen L. Bearne
, Org. Biomol. Chem.
, 2019
, 17
, 8618
- Azobenzene-based unnatural amino acid scaffolds via a Pd(ii)-catalyzed C(sp3)–H arylation strategy. Radha Tomar, Sonam Suwasia, Angshuman Roy Choudhury, Sugumar Venkataramani, Srinivasarao Arulananda Babu
, Chem. Commun.
, 2022
, 58
, 12967
- Optical studies of the Soret effect. Part III. Entropies and heat capacities of transfer of norvaline, ε-aminocaproic acid, L-proline, DL-hydroxyproline, and glycylglycine in aqueous solution. M. Kennerley, H. J. V. Tyrrell, M. Zaman
, J. Chem. Soc. A
, 1966
, 1041