https://nova.newcastle.edu.au/vital/access/ /manager/Index en-au 5 Triterpenes from Pittosporum resiniferum hemsl https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:29887 Wed 11 Apr 2018 15:32:28 AEST ]]> Triterpenes from Hoya paziae Kloppenb https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:29244 Wed 11 Apr 2018 14:36:51 AEST ]]> Secondary metabolites from Dracontomelon dao (Merr. & Rolfe) https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:26018 Wed 11 Apr 2018 14:02:12 AEST ]]> Chemical constituents of phellinus gilvus (Schwein.) Pat. https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:26019 13C NMR data with literature data.]]> Wed 11 Apr 2018 13:51:21 AEST ]]> Chemical constituents of Melanolepis multiglandulosa (Reinw. Ex blume) https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:29209 Wed 11 Apr 2018 10:38:20 AEST ]]> Chemical constituents of Alstonia scholaris (L.) R. Br https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:29211 Sat 24 Mar 2018 07:36:47 AEDT ]]> Sterols from Trametes versicolor https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:30602 Trametes versicolor yielded ergosterol peroxide (1) and a mixture of stellasterol (2) and ergosterol (3) in a 3.6:1 ratio. The structures of 1-3 were identified by comparison of their NMR data with literature data.]]> Sat 24 Mar 2018 07:28:28 AEDT ]]> Chemical constituents of Hoya paziae Kloppenb https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:30610 Hoya paziae Kloppenb. led to the isolation of a mixture of lupeol (1a), α-amyrin (1b), and β-amyrin (1c) in a 2:3:1 and a mixture of lupeol fatty acid esters (2a) α-amyrin fatty acid esters (2b) and β-amyrin fatty acid esters (2c) in a 3:2:1 ratio. The structures of 1a-2c were identified by comparison of their NMR data with those reported in the literature.]]> Sat 24 Mar 2018 07:28:27 AEDT ]]> Chemical constituents of Ficus septica Burm. F. https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:26698 Ficus septica Burm.f. led to the isolation of β-sitosteryl-3β-glucopyranoside-6'-O-fatty acid esters (1), α-amyrin fatty acid esters (2), and a mixture of β-sitosterol (3a) and stigmasterol (3b) in a 5: 2 ratios from the twigs; and 3a, β-amyrin (4), and long chain saturated fatty alcohols (5) from the leaves. The structures of 1-5 were identified by NMR spectroscopy.]]> Sat 24 Mar 2018 07:26:24 AEDT ]]> Isolation and structure elucidation of 9-hydroxy-10E, 12Z-octadecadienoic acid from Dioscorea luzonensis https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:26694 Sat 24 Mar 2018 07:26:23 AEDT ]]>