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- Substrate selectivity of an isolated enoyl reductase catalytic domain from an iterative highly reducing fungal polyketide synthase reveals key components of programming. Douglas M. Roberts, Christoph Bartel, Alan Scott, David Ivison, Thomas J. Simpson, Russell J. Cox
, Chem. Sci.
, 2017
, 8
, 1116
- Effect of the Cα substitution on the ketonic decarboxylation of carboxylic acids over m-ZrO2: the role of entropy. B. Oliver-Tomas, F. Gonell, A. Pulido, M. Renz, M. Boronat
, Catal. Sci. Technol.
, 2016
, 6
, 5561
- Catalytic mechanism of acetolactate decarboxylase from Brevibacillus brevis towards both enantiomers of α-acetolactate. Chenxiao Zhao, Hao Su, Yongjun Liu
, RSC Adv.
, 2016
, 6
, 80621
- Asymmetric hydrogenation of an α-unsaturated carboxylic acid catalyzed by intact chiral transition metal carbonyl clusters – diastereomeric control of enantioselectivity. Ahmed F. Abdel-Magied, Yusuf Theibich, Amrendra K. Singh, Ahibur Rahaman, Isa Doverbratt, Arun K. Raha, Matti Haukka, Michael G. Richmond, Ebbe Nordlander
, Dalton Trans.
, 2020
, 49
, 4244
- Studies on structure-function relationships of acetolactate decarboxylase from Enterobacter cloacae. Fangling Ji, Yanbin Feng, Mingyang Li, Yongliang Yang, Tianqi Wang, Jingyun Wang, Yongming Bao, Song Xue
, RSC Adv.
, 2018
, 8
, 39066
- Diastereomeric control of enantioselectivity: evidence for metal cluster catalysis. Ahmed F. Abdel-Magied, Amrendra K. Singh, Matti Haukka, Michael G. Richmond, Ebbe Nordlander
, Chem. Commun.
, 2014
, 50
, 7705
- Chemistry of the pheromones of mealybug and scale insects. Yunfan Zou, Jocelyn G. Millar
, Nat. Prod. Rep.
, 2015
, 32
, 1067
- Synthesis of some optically active thiazole derivatives. Luciano Lardicci, Carlo Battistini, Rita Menicagli
, J. Chem. Soc., Perkin Trans. 1
, 1974
, 344
- Chirally-modified metal surfaces: energetics of interaction with chiral molecules. Petr Dementyev, Matthias Peter, Sergey Adamovsky, Swetlana Schauermann
, Phys. Chem. Chem. Phys.
, 2015
, 17
, 22726
- Syntheses of isotopically labelled L-α-amino acids with an asymmetric centre at C-3. John R. Harding, Rachael A. Hughes, Nicholas M. Kelly, Andrew Sutherland, Christine L. Willis
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 3406