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240Afnan Al-Hunaiti, Teemu Niemi, Ahlam Sibaouih, Petri Pihko, Markku Leskelä and Timo Repo.
Solvent free oxidation of primary alcohols and diols using thymine iron(iii), Chem. Commun., 2010, 46, 9250. Adrian O. Chapman, Geoffrey R. Akien, Nicholas J. Arrowsmith, Peter Licence and Martyn Poliakoff.
Continuous heterogeneous catalytic oxidation of primary and secondary alcohols in scCO, Green Chem., 2010, 12, 310. Martin Karabec, Andrzej Łyskowski, Katharina C. Tauber, Georg Steinkellner, Wolfgang Kroutil, Gideon Grogan and Karl Gruber.
Structural insights into substrate specificity and solvent tolerance in alcohol dehydrogenase ADH-‘A’ from Rhodococcus ruber DSM 44541, Chem. Commun., 2010, 46, 6314. Charlie Van Doorslaer, Yves Schellekens, Pascal Mertens, Koen Binnemans and Dirk De Vos.
Spontaneous product segregation from reactions in ionic liquids: application in Pd-catalyzed aliphatic alcohol oxidation, Phys. Chem. Chem. Phys., 2010, 12, 1741. Jinbo Gao, Yongna Zhang, Guoqing Jia, Zongxuan Jiang, Shouguo Wang, Hongying Lu, Bo Song and Can Li.
A direct imaging of amphiphilic catalysts assembled at the interface of emulsion droplets using fluorescence microscopy, Chem. Commun., 2008, 332. Christina Kohlmann, Susanne Leuchs, Lasse Greiner and Walter Leitner.
Continuous biocatalytic synthesis of (R)-2-octanol with integrated product separation, Green Chem., 2011, 13, 1430. Christina Kohlmann, Nora Robertz, Susanne Leuchs, Lasse Greiner and Shukralla Na’amnieh.
Utilising hardly-water soluble substrates as a second phase enables the straightforward synthesis of chiral alcohols, Green Chem., 2011, 13, 3093. Frank Hollmann, Isabel W. C. E. Arends and Dirk Holtmann.
Enzymatic reductions for the chemist, Green Chem., 2011, 13, 2285. Marrit Eckstein, Murillo Villela Filho, Andreas Liese and Udo Kragl.
Use of an ionic liquid in a two-phase system to improve an alcohol dehydrogenase catalysed reduction, Chem. Commun., 2004, 0, 1084.