By Bo Mattiasson, Lei Ye
Managed radical polymerization strategies for molecular imprinting, by way of Mark E. Byrne
From bulk polymers to nanoparticles, by way of Lei Ye
Post-imprinting and in-cavity functionalization, by way of Toshifumi Takeuchi
Characterization of MIPs (affinity, selectivity, website heterogeneity…), by means of Richard Ansell
Theoretical facets and machine modelling, through Ian Nicholls
MIPs in aqueous environments, by means of Bin Lu
MIPs for binding macromolecules, by way of Kenneth J. Shea
Solid part extraction, through Ecevit Yilmaz
Sensors, via Sergey A. Piletsky
MIPs for catalysis and synthesis, through Marina Resmini
Wastewater therapy, via Bo Mattiasson
MIPs as instruments for bioassays, biotransformation and drug supply, by way of Meiping Zhao
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Extra info for Advances In Biochemical Engineering Biotechnology Biotransformations
Wamerdam EGJC, van den Nieuwendijk AMCH, Brussee J, Kruse CG, van der Gen A (1996) Tetrahedron: Asymmetry 7:2539 120. Johnson DV, Griengl H (1997) Tetrahedron 53:617 121. Johnson DV, Griengl H (1997) Abstract No P I-52, 3rd International Symposium on Biocatalysis and Biotransformations, 22–26 September, Le Grand Motte, France Club. Bioconversions en Synthese Organique, CNRS Marseille 122. Effenberger F, Jäger J (1997) J Org Chem 62:3867 Received February 1998 Stereoinversions Using Microbial Redox-Reactions Andrew J.
Johnson · H. Griengl Fig. 3. Examples of bioactive compounds synthesised from cyanohydrins Therefore, the chiral cyanohydrins are valuable and versatile synthons as their single hydroxyl asymmetric centre is accompanied by at least one other chemical functionality. Thus with careful functional group protection, differential and selective chemical transformations can be performed. Such synthetic techniques lead to production of interesting bioactive compounds and natural products. These products include intermediates of b-blockers 15 , b-hydroxy-a-amino acids 16 , chiral crown ethers 17 , coriolic acid 18 , sphingosines 19 , and bronchodilators such as salbutamol 20  (Fig.
1 Deracemization of Compounds with One Stereocentre . . . . 2 Deracemization of Compounds with Two Stereocentres . . . . 66 4 Regiospecific Stereoinversions in Sugar Biosynthesis . . . . . 69 5 Conclusions . . . . . . . . . . . . . . . . 71 6 References . . . . . . . . . . . . . . . . . 71 Advances in Biochemical Engineering / Biotechnology, Vol. 63 Managing Editor: Th. J. Carnell 1 Introduction Current regulations governing the introduction of chiral molecules as pharmaceuticals or agrochemicals require that each enantiomer should undergo testing for biological activity prior to development and marketing .
Advances In Biochemical Engineering Biotechnology Biotransformations by Bo Mattiasson, Lei Ye