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Brian W. Skelton

Researcher at University of Western Australia

Publications -  1662
Citations -  33374

Brian W. Skelton is an academic researcher from University of Western Australia. The author has contributed to research in topics: Crystal structure & Ligand. The author has an hindex of 69, co-authored 1646 publications receiving 31889 citations. Previous affiliations of Brian W. Skelton include Monash University, Clayton campus & State University of Malang.

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The Rare Earth(III) Nitrate Dimethyl Sulfoxide Adducts [( dmso )nLn(O2NO)3]

TL;DR: In this article, a series of room-temperature single-crystal X-ray studies were conducted on the dmso adducts obtained by the crystallizatior of lanthanoid (III) nitrate (Ln (NO3)3.-xH2O) with excess dimethyl sulfoxide ('dmso ') in methanol or ethanol, defining more clearly the manner in which stoichiometry and structure systematically vary with change in metal ion radius.
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Functionalization of cage amines with pendant aromatic and heteroaromatic substituents

TL;DR: Structural studies have confirmed that it is possible to exploit the relatively low nucleophilicity of the “external” amino substituents on the CoIII complex of 1,8-diaminosarcophagine in acylation and alkylation reactions leading to a variety of functionalized cage amine complexes.
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A Compact Approach to an Isomeric Iheyamine A System and X-ray Crystal Structure of 5-Methyl-5H-azepino[2,3- b :4,5- b ′]diindole

TL;DR: In this article, a three-step synthesis of a new fused bisindole system isomeric with the heterocyclic skeleton present in the marine natural product iheyamine A has been achieved.
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Porphyrin–crown ether based macrocyclic receptors for bipyridinium cations

TL;DR: In this paper, a porphyrin strapped by a single dibenzo crown ether and two benzo-15-crown-5 units was reported to be able to complex the bipyridinium cations paraquat, diquat, and [Pt(bpy)(NH3)2]2]-2+ in two different configurations.
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Ethynylbenzenoid metabolites of Antrodia camphorata : synthesis and inhibition of TNF expression

TL;DR: An improved synthesis of the anti-inflammatory natural product antrocamphin A, involving a key Castro-Stephens reaction, is presented, along with the first total synthesis of its congener antrocampshin B.