Zobrazeno 1 - 10
of 141
pro vyhledávání: '"AL Wilkins"'
Publikováno v:
Yearbook of Paediatric Endocrinology.
Publikováno v:
ChemInform. 21
Publikováno v:
Australian Journal of Chemistry. 43:191
The new lichen depsides, 2′-O-methylnorbarbatic acid (9) and 2′-O-methylnorobtusatic acid (12) have been detected in Pseudocyphellaria norvegica and the structures confirmed by total synthesis. In addition, the known depsides 4-O-demethylbarbatic
Publikováno v:
Australian Journal of Chemistry. 42:243
The phase sensitive two-dimensional (2D) 13C-1H heteronuclear correlated and double quantum filtered cosy n.m.r. spectra of the triterpenes 7β-acetoxyhopan-22-ol and 2 α,3 β,22 α- triacetoxystictane have been recorded at a resolution sufficient f
Autor:
AL Wilkins, EM Goh
Publikováno v:
Australian Journal of Chemistry. 41:143
The crystal structure of 22α-hydroxystictan-3-one has been determined by X-ray diffraction. Rings A and B of this keto alcohol have been shown to adopt twist boat conformations. Despite the presence of the twist boat ring A system photochemical rear
Publikováno v:
Australian Journal of Chemistry. 40:2023
The new depsides 2'- O- methylphenarctin (6), 1'-chloronephroarctin (7), 2'- O- methylpseudo-cyphellarin A (3), isopseudocyphellarin A (8) and 2'- O- methylisopseudocyphellarin A (9), have been isolated from New Zealand collections of the lichen Pseu
Publikováno v:
Australian Journal of Chemistry. 29:2567
The structure of retigeradiol, a triterpenoid diol previously considered to be taraxerane-3β,19β-diol, is revised to that of stictane-3β,22α-diol.
Autor:
RE Corbett, AL Wilkins
Publikováno v:
Australian Journal of Chemistry. 30:2329
The hopane triterpenoid in the extractives from P. mougeotiana, reported in Part VII1 of this series as hopane-6α,7α,22-triol, is now shown to be hopane-6α,7β,22-triol (1j). There is a consequential revision of the two triol diacetate structures
Publikováno v:
Australian Journal of Chemistry. 40:1713
Chemical shift assignments are reported for some hopane triterpenoids variously oxygenated at C3, C6, C7, C15, C22 and/or C24. Substituent group effects are compared and correlated with a local symmetry axis. Revisions to a recently reported interpre
Publikováno v:
Australian Journal of Chemistry. 42:1185
A complete assignment of the 1H and 13C n.m.r. signals of the lichen triterpenoid 12α-acetoxyfern-9(11)-en-3 β-ol (lb) has been achieved by using one- and two-dimensional n.m.r. techniques. Evidence in support of one of two recently advanced assign