Publications: complete list
Showing results 481 - 490 out of 942
2014
Al Fahad, A., Abood, A., Fisch, K. M., Osipow, A., Davison, J., Avramović, M., Butts, C. P., Piel, J., Simpson, T. J., & Cox, R. J. (2014). Oxidative dearomatisation: The key step of sorbicillinoid biosynthesis. Chemical science, 5(2), 523-527. https://doi.org/10.1039/c3sc52911h
Al Fahad, A., Abood, A., Simpson, T. J., & Cox, R. J. (2014). The biosynthesis and catabolism of the maleic anhydride moiety of stipitatonic acid. Angewandte Chemie , 53(29), 7519-7523. https://doi.org/10.1002/anie.201403450, https://doi.org/10.1002/ange.201403450
Butenschön, H. (2014). CHEMKON volljährig! Chemkon, 21(4), 161-161. https://doi.org/10.1002/ckon.201410235
Chaudhuri, S. R., Hartwig, J., Kupracz, L., Kodanek, T., Wegner, J., & Kirschning, A. (2014). Oxidations of allylic and benzylic alcohols under inductively-heated flow conditions with gold-doped superparamagnetic nanostructured particles as catalyst and oxygen as oxidant. Advanced Synthesis and Catalysis, 356(17), 3530-3538. https://doi.org/10.1002/adsc.201400261
Collemare, J., Griffiths, S., Iida, Y., Karimi Jashni, M., Battaglia, E., Cox, R. J., & De Wit, P. J. G. M. (2014). Secondary metabolism and biotrophic lifestyle in the tomato pathogen Cladosporium fulvum. PLOS ONE, 9(1), Article e85877. https://doi.org/10.1371/journal.pone.0085877
Cox, R. (2014). Oxidative rearrangements during fungal biosynthesis. Natural product reports, 31(10), 1405-1424. https://doi.org/10.1039/c4np00059e
Cox, R. J. (2014). β-Chain extension: A new mode of carbon-carbon bond formation and chain extension by polyketide synthases. CHEMBIOCHEM, 15(1), 27-29. https://doi.org/10.1002/cbic.201300660, https://doi.org/10.1002/cbic.201300660
Geist, E., Kirschning, A., & Schmidt, T. (2014). Sp3-sp3 Coupling reactions in the synthesis of natural products and biologically active molecules. Natural Product Reports, 31(4), 441-448. https://doi.org/10.1039/c3np70108e
Gerke, J., & Braus, G. H. (2014). Manipulation of fungal development as source of novel secondary metabolites for biotechnology. Applied Microbiology and Biotechnology, 98(20), 8443-8455. https://doi.org/10.1007/s00253-014-5997-8
Gieseler, M. T., & Kalesse, M. (2014). Synthesis of angiolam A. Organic letters, 16(2), 548-551. https://doi.org/10.1021/ol403423r
