Showing results 71 - 80 out of 196
2018
De Mattos-Shipley, K. M. J., Greco, C., Heard, D. M., Hough, G., Mulholland, N. P., Vincent, J. L., Micklefield, J., Simpson, T. J., Willis, C. L., Cox, R. J., & Bailey, A. M. (2018). The cycloaspeptides: uncovering a new model for methylated nonribosomal peptide biosynthesis. Chemical science, 9(17), 4109-4117. https://doi.org/10.1039/c8sc00717a, https://doi.org/10.15488/3457
He, Y., Wang, B., Chen, W., Cox, R. J., He, J., & Chen, F. (2018). Recent advances in reconstructing microbial secondary metabolites biosynthesis in Aspergillus spp. Biotechnology advances, 36(3), 739-783. https://doi.org/10.1016/j.biotechadv.2018.02.001
Schor, R., & Cox, R. (2018). Classic fungal natural products in the genomic age: the molecular legacy of Harold Raistrick. Natural product reports, 35(3), 230-256. https://doi.org/10.1039/c8np00021b, https://doi.org/10.15488/3311
2017
Essoung, F. R. E., Mba'ning, B. M., Lwande, W., Ngouela, S. A., Tsamo, E., Chhabra, S. C., Hassanali, A., & Cox, R. J. (2017). Welwitschianalol A and B, two cyclohexene derivatives and other insecticidal constituents of Caesalpinia welwitschiana (Oliv.) Brenan. Phytochemistry letters, 22, 81-86. https://doi.org/10.1016/j.phytol.2017.09.010
Trenti, F., & Cox, R. J. (2017). Structural Revision and Biosynthesis of the Fungal Phytotoxins Phyllostictines A and B. Journal of natural products, 80(5), 1235-1240. https://doi.org/10.1021/acs.jnatprod.7b00183
Gao, S. S., Wang, L., Song, Z., Hothersall, J., Stevens, E. R., Connolly, J., Winn, P. J., Cox, R. J., Crump, M. P., Race, P. R., Thomas, C. M., Simpson, T. J., & Willis, C. L. (2017). Selected Mutations Reveal New Intermediates in the Biosynthesis of Mupirocin and the Thiomarinol Antibiotics. Angewandte Chemie , 56(14), 3930-3934. https://doi.org/10.1002/anie.201611590, https://doi.org/10.1002/ange.201611590
Feng, J., Zhang, P., Cui, Y., Li, K., Qiao, X., Zhang, Y. T., Li, S. M., Cox, R. J., Wu, B., Ye, M., & Yin, W. B. (2017). Regio- and Stereospecific O-Glycosylation of Phenolic Compounds Catalyzed by a Fungal Glycosyltransferase from Mucor hiemalis. Advanced Synthesis and Catalysis, 359(6), 995-1006. https://doi.org/10.1002/adsc.201601317, https://doi.org/10.1002/adsc.201701070
Williams, K., Szwalbe, A. J., Dickson, C., Desson, T. R., Mulholland, N. P., Vincent, J. L., Clough, J. M., Bailey, A. M., Butts, C. P., Willis, C. L., Simpson, T. J., & Cox, R. J. (2017). Genetic and chemical characterisation of the cornexistin pathway provides further insight into maleidride biosynthesis. Chemical communications, 53(56), 7965-7968. https://doi.org/10.1039/c7cc03303f
Liddle, E., Scott, A., Han, L. C., Ivison, D., Simpson, T. J., Willis, C. L., & Cox, R. J. (2017). In vitro kinetic study of the squalestatin tetraketide synthase dehydratase reveals the stereochemical course of a fungal highly reducing polyketide synthase. Chemical communications, 53(10), 1727-1730. https://doi.org/10.1039/c6cc10172k
Chen, W., Chen, R., Liu, Q., He, Y., He, K., Ding, X., Kang, L., Guo, X., Xie, N., Zhou, Y., Lu, Y., Cox, R. J., Molnár, I., Li, M., Shao, Y., & Chen, F. (2017). Orange, red, yellow: Biosynthesis of azaphilone pigments in Monascus fungi. Chemical science, 8(7), 4917-4925. https://doi.org/10.1039/c7sc00475c
