Al-Dulayymi,Juma
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My research activity is focused on the synthesis of individual synthetic mycolic acids and their sugar esters, and in collaboration with other groups examining their biological activity. I am also interested in the synthesis of cyclopropenes and their applications and the identification, isolation and modification of natural products from plants.近期论文
68. The synthesis of a single enantiomers of trans-alkene containing mycolic acid, G. Koza, H. M. Ali, R. T. Hameed, R. Rowles, Carys Davies, Juma’a R. Al Dulayymi, C.D. Gwenin and Mark S. Baird; Tetrahedron, 2016 in press67. Standardization of natural mycolic acid antigen composition and production for use in biomarker antibody detection to diagnose active tuberculosis, F.L. Ndlandla, V. Ejoh, A.C.Stoltz, B. Naicker, A.D. Cromarty, S. van Wyngaardt, M. Khati, L.S. Rotherham, Y. Lemmer, J. Niebuhr, C.R. Baumeister, Jumaa R. Al Dulayymi, H. Swai, M.S. Baird and J.A. Verschoor; Journal of Immunological Methods, 2016, 435, 50-59.66. Sterculic acid and its analogues are potent inhibitors of Toxoplasma gondii, P. Hao, I. Q. M. Alaragi, Juma’a R. Al Dulayymi, M. S. Baird, J. Liu and Q. Liu; Korean J Parasitol, 2016, 54, 139.65. Synthesis of Wax esters and related sugar esters from Mycobacterium avium and other mycobacteria, S. G. Taher, Juma’a R. Al Dulayymi, A. Jones, H. M. Ali, Mark S. Baird, Tetrahedron; 2016, 72, 386364. Arabino Mycolates from Synthetic Mycolic acids, M. Mohammed, Mark S. Baird, Juma’a R. Al Dulayymi, A. Jones and C.D. Gwenin; Tetrahedron, 2016 ,72, 284963. Synthesis of glucose monomycolates based on single synthetic mycolic acids, M. M. Sahb, Juma’a R. Al Dulayymi and Mark S. Baird; Chemistry and physics of Lipids; 2015, 190, 962. Synthetic trehalose esters of cis-alkene and diene α’-mycolic acids of Mycobacteria, S. G. Taher, M. Muzael, Juma’a R. Al Dulayymi and Mark S. Baird; Chemistry and physics of Lipids; 2015, 189, 2861. Mycolyl arabino glycerols from synthetic mycolic acid, M. O. Mohammed, Mark S. Baird and Juma’a R. Al Dulayymi; Tetrahedron Lett., 2015, 56, 326860. Synthetic trehalose di- and mono-ester of α-, Methoxy-, and Keto-mycolic acids, Juma’a R. Al-Dulayymi, Maximiliano Maza-Iglesias, M.S.Baird, Rwoa’a T. Hameed, Klarah S. Baols, Majed Muzael, and Ahmad D. Saleh; Tetrahedron, 2014, 70, 9836.59. Synthetic epoxy-mycolic acids, Dakhil Z. Al-Kremawi, Juma’a R. Al-Dulayymi and Mark S. Baird. Tetrahedron, 2014, 70, 732258. A nine carbon homologating system for skip-conjugated polyenes, Hussain H. Mustafa, Mark S. Baird, Juma’a R. Al-Dulayymi and V. V. Tverezovskiy; Chemistry and physics of Lipids; 2014, 183, 34-42.57. Tandem rearrangements of a cyclic bis-allene, Hussain H. Mustafa, Mark S. Baird, Juma’a R. Al-Dulayymi and V. V. Tverezovskiy; Tetrahedron, 2014, 70, 1502.56. The synthesis of methoxy and keto mycolic containing methyl-trans-cyclopropanes, G. Koza, M. Muzael, R. R. Schubert-Rowles, C. Theunissen, Juma’a R. Al-Dulayymi and Mark S. Baird; Tetrahedron, 2013, 69, 6285.55. Thiol modified Mycolic acids, M. M. Balogun, E. H. Huws, M. M. Sirhan, A. D. Saleh, Juma’a R. Al-Dulayymi, L. Pilcher, J. A. Verschoor and Mark S. Baird; Chemistry and physics of Lipids; 2013, 172-173, 40-57.54. Diastereomeric cyclic tris-allenes, Hussain H. Mustafa, Mark S. Baird, Juma’a R. Al-Dulayymi and V. V. Tverezovskiy; J. Chemical Socity, Chem. Commun., 2013, 49, 2497.53. Structure-function relationships of the antigenicity of mycolic acids in tuberculosis patients, M. Beukes, Y. Lemmer, M. Deysel, Juma’a R. Al-Dulayymi, M. S. Baird, G. Koza, M. M. Iglesisa, R. R. Rowles, C. Theunissen, J. Grooten, G. Toschi, V.V. Roberts, L. Pilcher, S. V. Wyngaardt, N. Mathebula, M. Balogun, A. C. Stoltz and J. Verschoor, Chemistry and physics of lipids, 2010, 163, 800.52. The synthesis of a major α’-mycolic acid of Mycobacterium smegmatis, Maged Muzael, Gani Koza, Juma’a R Al Dulayymi, Mark S. Baird, Chemistry and physics of lipids, 2010, 163, 678.51. Molecular structure of the Mycobacterium tuberculosis virulence factor, mycolic acid, determines the elicited inflammatory pattern., S.V.Beken, Juma’a R. Al-Dulayymi, T.rt, T.Naessens, G.Koza, M.M.Iglesisa, R. Rowles, C.Theunissen, J. De Medts, E.Lanckacker, M.S.Baird and J.Grooten; European Journal of Immunology, 2011, 41, 450.50. The first synthesis of epoxy-mycolic acids, Dakhil Z. Al-Kremawi, Juma’a R. Al-Dulayymi and Mark S. Baird. Tetrahedron Letts., 2010, 51, 1698. 49. The synthesis of a single enantiomers of protected trans-alkene containing mycolic acid, G. Koza, R. Rowles, C. Theunissen, Juma’a R. Al-Dulayymi and Mark S. Baird, Tetrahedron Letts., 2009, 65, 7259.48. The first synthesis of single enantiomers of the keto mycolic acids, G. Koza, C.Theunissen, Juma’a R. Al-Dulayymi and Mark S. Baird. Tetrahedron, 2009, 65, 10214.47. The first unique synthetic mycobacterial cord factor, Juma’a R. Al-Dulayymi, Maximiliano Maza-Iglesias, M.S.Baird, Seppe Vander Beken and John Grooten; Tetrahedron Letters, 2009, 50, 3702.46. The first synthesis of single enantiomers of the major methoxymycolic acid of Mycobacterium tuberculosis, Juma’a R. Al-Dulayymi, M.S.Baird, E.Roberts, M.Dreysel and J.Verschoor. Tetrahedron. 2007, 63, 2571,45. The synthesis of a single enantiomers of meromycolic acids from mycobacterial wax esters., Juma’a R. Al-Dulayymi, M.S.Baird, E.Roberts and D. E. Minnikin. Tetrahedron, 2006, 62, 11867.44. The synthesis of one enantiomer of the α-methyl-trans-cyclopropane unit of mycolic acids, Juma’a R. Al-Dulayymi, M.S.Baird, H.M.Mohammed, E.Roberts and W.Clegg. Tetrahedron. 2006, 62, 4851.标签: 班戈大学
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