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- Metal-catalyzed reductive deamination of glutamic acid to bio-based dimethyl glutarate and methylamines. Free De Schouwer, Thomas Cuypers, Laurens Claes, Dirk E. De Vos
, Green Chem.
, 2017
, 19
, 1866
- Defluorination of 4-fluorothreonine by threonine deaminase. Linrui Wu, Hai Deng
, Org. Biomol. Chem.
, 2020
, 18
, 6236
- The synthesis and characterisation of hyperbranched poly(diethyl3-hydroxyglutarate). W. James Feast, Lesley M. Hamilton, Lois J. Hobson, Steve P. Rannard
, J. Mater. Chem.
, 1998
, 8
, 1121
- An on-line heart-cutting two-dimensional liquid chromatography method for intracellular 2-hydroxyglutarate enantiomers. Takuma Ohtawa, Makoto Tsunoda
, Anal. Methods
, 2023
, 15
, 2833
- Advances in microbial production of medium-chain dicarboxylic acids for nylon materials. Guohui Li, Dixuan Huang, Xue Sui, Shiyun Li, Bing Huang, Xiaojuan Zhang, Hui Wu, Yu Deng
, React. Chem. Eng.
, 2020
, 5
, 221
- Structural analysis of oncogenic mutation of isocitrate dehydrogenase 1. Vidya Rajendran
, Mol. BioSyst.
, 2016
, 12
, 2276
- Stereochemical studies on porphyrin a: assignment of the absolute configuration of a model porphyrin by degradation. Alan R. Battersby, Kevin S. Cardwell, Finian J. Leeper
, J. Chem. Soc., Perkin Trans. 1
, 1986
, 1565
- Maleic anhydride proton sponge as a novel MALDI matrix for the visualization of small molecules (<250 m/z) in brain tumors by routine MALDI ToF imaging mass spectrometry. M. GiampĂ , M. B. Lissel, T. Patschkowski, J. Fuchser, V. H. Hans, O. Gembruch, H. Bednarz, K. Niehaus
, Chem. Commun.
, 2016
, 52
, 9801
- A small-molecule probe for monitoring binding to prolyl hydroxylase domain 2 by fluorescence polarisation. Zhihong Li, Shuai Zhen, Kaijun Su, Anthony Tumber, Quanwei Yu, Ying Dong, Michael McDonough, Christopher J. Schofield, Xiaojin Zhang
, Chem. Commun.
, 2020
, 56
, 14199
- Design, synthesis and biological evaluation of novel 5-hydroxy-2-methyl-4H-pyran-4-one derivatives as antiglioma agents. Yi-Bin Li, Wen Hou, Hui Lin, Ping-Hua Sun, Jing Lin, Wei-Min Chen
, Med. Chem. Commun.
, 2018
, 9
, 471