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Date: 2008
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/1154201
Description: The Miriwoong Aboriginal people of Eastern Kimberley, Western Australia use the leaves and bark of Dolichandrone heterophylla (R. Br.) F. Muell., Bigoniaceae, to treat sores, rashes, grazes, scabies, ... More
Reviewed: Reviewed
Date: 2008
Subject Keyword: 030500 Organic Chemistry
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/1154060
Description: 8 page(s)
Reviewed: Reviewed
Date: 2008
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/84772
Description: Tröger’s base analogues are of interest in areas such as host-guest chemistry, synthetic receptor design and asymmetric catalysis. We foresee that access to diverse functionality attached to the bridg ... More
Full Text: Full Text
Reviewed: Reviewed
Date: 2008
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/1138405
Description: The three title reductant systems have significant advantages in generating aldehydes fromnitriles. These include: the utilization of convenient hydrogen sources, namely, sodium hypophosphite monohydr ... More
Reviewed: Reviewed
Date: 2007
Subject Keyword: 030500 Organic Chemistry
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/15744
Description: In the molecule of the title compound, C₁₉H₁₈N₆O₁₀, the 2,8-dimethoxy-4,10-dimethyl-1,3,7,9-tetranitro analogue of Tröger’s base, the diazocine bridge imparts a twist such that the two aryl rings are ... More
Full Text: Full Text
Reviewed: Reviewed
Date: 2007
Subject Keyword: 030500 Organic Chemistry
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/15777
Description: In the molecule of the title compound, C₁₇H₁₆N₄O₄, the 2,8-dimethyl-1,9-dinitro analogue of Tröger’s base, the diazocine bridge imparts a twist such that the two aryl rings are offset with respect to ... More
Full Text: Full Text
Reviewed: Reviewed
Date: 2007
Subject Keyword: 030500 Organic Chemistry
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/16923
Description: A multi-gram synthesis of a substituted α, β-unsaturated δ-lactone synthon, 1, was developed from commercially available D-galactose. The use of a Horner–Wadsworth–Emmons reaction was able to furnish, ... More
Reviewed: Reviewed
Authors: Yang, Minghua | Liu, Fei
Date: 2007
Subject Keyword: 030500 Organic Chemistry
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/16933
Description: A copper-based catalytic system, using an air-stable diazaphospholane as the ligand, was developed for an efficient Ullmann reaction between aryl iodides and alkyl or heterocyclic amines.
Reviewed: Reviewed
Date: 2007
Subject Keyword: 030500 Organic Chemistry
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/23374
Description: A facile synthesis of β-functionalized γ-hydroxybutenolides was achieved using a Baylis-Hillman reaction followed by singlet oxygen oxidation. The conversion from 3-furfural was regio- and diastereose ... More
Reviewed: Reviewed
Date: 2007
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/22178
Description: Late Cretaceous sandstones from the Subu-1 and -2 wells (Aure Scarp, Papua New Guinea) contain patchily distributed solid bitumens. The solid bitumens vary in reflectance and geochemistry, indicating ... More
Reviewed: Reviewed
Date: 2007
Subject Keyword: 030500 Organic Chemistry
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/16918
Description: The first synthesis of Tröger’s base analogues bearing three and four atoms in the apical strap is reported, leading to a dramatic change in the shape of the aromatic scaffold with respect to the Trög ... More
Reviewed: Reviewed
Date: 2007
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/23354
Description: Fulvic acid ‘backbone’ structures were studied by subjecting fulvic acids isolated from Elliott soil, Suwannee River and Waskish peat to a selective reduction method. The products were subsequently an ... More
Reviewed: Reviewed
Date: 2007
Subject Keyword: 030500 Organic Chemistry
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/16928
Description: A facile synthesis of α-sutstituted γ-hydroxybutenolides from 3-furfural was achieved using a Baylis-Hillman reaction followed by singlet oxygen oxidation. The regioselectivity of this conversion was ... More
Reviewed: Reviewed
Date: 2007
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/22003
Description: Sulfinamides are important in enantioselective synthesis, as rare post-translational modifications of proteins and as isosteres of the amide bond. Little is known about the rates of hydrolysis for ali ... More
Reviewed: Reviewed