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- Unveiling sequential late-stage methyltransferase reactions in the meleagrin/oxaline biosynthetic pathway. Sean A. Newmister, Stelamar Romminger, Jennifer J. Schmidt, Robert M. Williams, Janet L. Smith, Roberto G. S. Berlinck, David H. Sherman
, Org. Biomol. Chem.
, 2018
, 16
, 6450
- Roquefortine, an intermediate in the biosynthesis of oxaline in cultures of Penicillium oxalicum. Pieter S. Steyn, Robert Vleggaar
, J. Chem. Soc., Chem. Commun.
, 1983
, 560
- Fundamental aspects of electrochemically controlled wetting of nanoscale composite materials. A. Robert Hillman, Karl S. Ryder, Hani K. Ismail, Asuman Unal, Annelies Voorhaar
, Faraday Discuss.
, 2017
, 199
, 75
- Stereochemistry of the dehydrogenation of (2S)-histidine in the biosynthesis of roquefortine and oxaline. Robert Vleggaar, Philippus L. Wessels
, J. Chem. Soc., Chem. Commun.
, 1980
, 160
- X-Ray structure of oxaline: a novel alkaloid from Penicillium oxalicum. Dietmar W. Nagel, Klaus G. R. Pachler, Pieter S. Steyn, Philippus L. Wessels, Geoffrey Gafner, Gert J. Kruger
, J. Chem. Soc., Chem. Commun.
, 1974
, 1021
- Solvation of carbohydrates in five choline chloride-based deep eutectic solvents and the implication for cellulose solubility. Riina Häkkinen, Andrew Abbott
, Green Chem.
, 2019
, 21
, 4673
- Status and advances of deep eutectic solvents for metal separation and recovery. Ziwen Yuan, Hang Liu, Wai Fen Yong, Qianhong She, Jesús Esteban
, Green Chem.
, 2022
, 24
, 1895
- Effect of solute polarity on extraction efficiency using deep eutectic solvents. Odeh A. O. Alshammari, Ghazi A. A. Almulgabsagher, Karl S. Ryder, Andrew P. Abbott
, Green Chem.
, 2021
, 23
, 5097
- CCXXXII.—Some derivatives of 4(or 5)-methylglyoxaline. Arthur James Ewins
, J. Chem. Soc., Trans.
, 1911
, 99
, 2052
- CCXL.—Gold and mercury derivatives of 2-thiolglyoxalines. Mechanism of the oxidation of 2-thiolglyoxalines to glyoxalines. Isidore Elkanah Balaban, Harold King
, J. Chem. Soc.
, 1927
, 1858