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Synthesis of 2‐Aminopyridine Derivatives via a Tandem CuAAC/Ring‐Cleavage/[4+2]‐Cycloaddition/Rearrangement Reaction Sequence.
- Published in:
- Advanced Synthesis & Catalysis, 2024, v. 366, n. 17, p. 3689, doi. 10.1002/adsc.202400339
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- Article
gem-Dibromocyclopropanes and enzymatically derived cis-1,2-dihydrocatechols as building blocks in alkaloid synthesis.
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- Pure & Applied Chemistry, 2012, v. 84, n. 6, p. 1329
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- Article
The Isoflavanoid (+)‐PTC Regulates Cell‐Cycle Progression and Mitotic Spindle Assembly in a Prostate Cancer Cell Line.
- Published in:
- Chemistry & Biodiversity, 2022, v. 19, n. 5, p. 1, doi. 10.1002/cbdv.202200102
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- Article
The synthesis and manipulation of certain Diels--Alder adducts of levoglucosenone and iso-levoglucosenone.
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- Australian Journal of Chemistry, 2023, v. 76, n. 11, p. 797, doi. 10.1071/CH23130
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- Article
Six-step total syntheses of (−)-galanthamine and (−)-N-norgalanthamine.
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- Australian Journal of Chemistry, 2022, v. 75, n. 12, p. 974, doi. 10.1071/CH22183
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- Article
Simple and modestly scalable synthesis of iso-Cyrene from levoglucosenone and its comparison to the bio-derived and polar aprotic solvent Cyrene<sup>®</sup>.
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- Australian Journal of Chemistry, 2022, v. 75, n. 5, p. 331, doi. 10.1071/CH22046
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- Article
The Synthesis, Structural Characterisation, and Chemoselective Manipulation of Certain Functionalised Cyclic Sulfates Derived from Chiral, Non-Racemic, and Polysubstituted Bicyclo[2.2.2]octane-2,3-diols.
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- Australian Journal of Chemistry, 2021, v. 74, n. 9, p. 640, doi. 10.1071/CH21140
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- Article
The Synthesis and Biological Evaluation of Some C-9 and C-10 Substituted Derivatives of the RNA Polymerase I Transcription Inhibitor CX-5461.
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- Australian Journal of Chemistry, 2021, v. 74, n. 7, p. 540, doi. 10.1071/CH21049
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- Article
Further, Small-Molecule Pyrolysis Products Derived from Chitin*.
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- Australian Journal of Chemistry, 2020, v. 73, n. 12, p. 1187, doi. 10.1071/CH20172
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- Article
Electrocyclic Ring-Opening of 6,6-Dichlorobicyclo[3.1.0]-hexanes and Trapping of the Resulting π-Allyl Cations by C-1 Tethered Hydroxyamine Derivatives: Formation of 2-Oxa-1-azaspiro[4.5]decan-3-ones.
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- Australian Journal of Chemistry, 2019, v. 72, n. 6, p. 434, doi. 10.1071/CH19010
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- Article
Synthetic Studies on the Marine-Derived Sesquiterpene (+)-Viridianol: Divergent Behaviour of Two Structurally Related, Ring-Fused Cyclopropanes Under the Same Hydrogenolytic Conditions.
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- Australian Journal of Chemistry, 2019, v. 72, n. 4, p. 305, doi. 10.1071/CH18532
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- Article
Chemoenzymatic Syntheses of Some Analogues of the Tricarbocyclic Core of the Anti-Bacterial Agent Platencin and the Biological Evaluation of Certain of their N-Arylpropionamide Derivatives*.
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- Australian Journal of Chemistry, 2018, v. 71, n. 9, p. 655, doi. 10.1071/CH18145
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- Article
Synthesis of a Highly Functionalised and Homochiral 2-Iodocyclohexenone Related to the C-Ring of the Polycyclic, Indole Alkaloids Aspidophytine and Haplophytine.
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- Australian Journal of Chemistry, 2018, v. 71, n. 8, p. 573, doi. 10.1071/CH18267
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- Article
New, Homochiral Synthons Obtained through Simple Manipulations of Enzymatically Derived 3-Halo-cis-1,2-dihydrocatechols.
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- Australian Journal of Chemistry, 2015, v. 68, n. 10, p. 1467, doi. 10.1071/CH15061
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- Article
The Palladium-Catalysed Intramolecular Alder-ene (IMAE) Reactions of Certain Heteroatom-Linked 1,6-Enynes: The Formation of Hexahydro-Indoles and -Benzofurans*.
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- Australian Journal of Chemistry, 2015, v. 68, n. 8, p. 1183, doi. 10.1071/CH15340
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- Article
The Conversion of Levoglucosenone into Isolevoglucosenone.
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- Australian Journal of Chemistry, 2015, v. 68, n. 4, p. 593, doi. 10.1071/CH14574
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- Article
A Chemoenzymatic Route to the (+)-Form of the Amaryllidaceae Alkaloid Narseronine.
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- Australian Journal of Chemistry, 2015, v. 68, n. 2, p. 241, doi. 10.1071/CH14520
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- Article
Synthetic Studies Concerning the Crinine Alkaloid Haemultine Synthetic Studies on the Alkaloid Haemultine N. Gao et al.
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- Australian Journal of Chemistry, 2013, v. 66, n. 1, p. 30, doi. 10.1071/CH12473
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- Article
Probing for the Pharmacophore of the Cytotoxic Neoclerodane Salvileucalin B.
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- Australian Journal of Chemistry, 2012, v. 65, n. 12, p. 1679, doi. 10.1071/CH12358
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- Article
Synthesis of 2,3-Dihydro-4(1H)-quinolones and the Corresponding 4(1H)-Quinolones via Low-Temperature Fries Rearrangement of N-Arylazetidin-2-ones.
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- Australian Journal of Chemistry, 2011, v. 64, n. 4, p. 454, doi. 10.1071/CH10465
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- Article
Total Syntheses of Favolasins A, E, G and K, Polyketides Isolated from Cultures of the Basidiomycetes Fungi Favolaschia sp. BCC 18686 and Favolaschia caloceraBCC 36684.
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- Chinese Journal of Chemistry, 2023, v. 41, n. 12, p. 1450, doi. 10.1002/cjoc.202200822
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- Article
Front Cover: Synthesis and Ring‐Closing Reactions of Aminocyclohexane Derivatives Bearing Unsaturated Side Chains at C2: Stereocontrolled Approaches to cis‐ and trans‐Fused Perhydro‐indoles and ‐quinolines (Eur. J. Org. Chem. 33/2024)
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- European Journal of Organic Chemistry, 2024, v. 27, n. 33, p. 1, doi. 10.1002/ejoc.202483301
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- Article
Synthesis and Ring‐Closing Reactions of Aminocyclohexane Derivatives Bearing Unsaturated Side Chains at C2: Stereocontrolled Approaches to cis‐ and trans‐Fused Perhydro‐indoles and ‐quinolines.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 33, p. 1, doi. 10.1002/ejoc.202400455
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- Article
A gem‐Dibromocyclopropane Ring‐Expansion/Mizoroki‐Heck Cyclisation Route to Tetrahydrodibenzofurans.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 9, p. 1, doi. 10.1002/ejoc.202400038
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- Article
Approaches to the Neurotrophically Active Natural Product 11- O-Debenzoyltashironin: A Chemoenzymatic Total Synthesis of the Structurally Related Sesquiterpene Khusiol.
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- Chemistry - An Asian Journal, 2012, v. 7, n. 4, p. 676, doi. 10.1002/asia.201100913
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- Article
gem-Dihalocyclopropanes as Building Blocks in Natural-Product Synthesis: Enantioselective Total Syntheses of ent-Erythramine and 3- epi-Erythramine.
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- Chemistry - An Asian Journal, 2007, v. 2, n. 9, p. 1127, doi. 10.1002/asia.200700155
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- Article
Antimicrobial and Cytotoxic Activities of Synthetically Derived Tambjamines C and E - J, BE-18591, and a Related Alkaloid from the Marine Bacterium Pseudoalteromonas tunicata.
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- Chemistry & Biodiversity, 2010, v. 7, n. 5, p. 1311, doi. 10.1002/cbdv.201000030
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- Article
Biological Evaluation of ent-Narciclasine, ent-Lycoricidine, and Certain Enantiomerically-Related Congeners.
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- Chemistry & Biodiversity, 2009, v. 6, n. 5, p. 685, doi. 10.1002/cbdv.200800319
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- Article
Ribisins and Certain Analogues Exert Neuroprotective Effects through Activation of the Keap1‐Nrf2‐ARE Pathway.
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- ChemMedChem, 2022, v. 17, n. 18, p. 1, doi. 10.1002/cmdc.202200292
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- Article
The Effects of the Alkaloid Tambjamine J on Mice Implanted with Sarcoma 180 Tumor Cells.
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- ChemMedChem, 2021, v. 16, n. 2, p. 420, doi. 10.1002/cmdc.202000387
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- Article
Syntheses and Preliminary Biological Evaluations of the Dibromopyrrole‐Containing Marine Natural Products Agesasine A, Agesasine B, Longamide E and Various Congeners.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 16, p. 1, doi. 10.1002/ejoc.202300003
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- Article
Synthetic Studies Concerned with the Proposed Structure of Ribisin F, a Compound with Nerve Growth Factor Potentiating Activity Isolated from the Medicinal Fungus Phellinus ribis.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 13, p. 1, doi. 10.1002/ejoc.202300010
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- Article
Total Syntheses of the Imidazo[1,2‐f]phenanthridine‐Containing Alkaloid Zephycandidine A.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 9, p. 1, doi. 10.1002/ejoc.202101511
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- Article
Synthesis of Pyridin-1(2 H)-ylacrylates and the Effects of Different Functional Groups on Their Fluorescence.
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- Molecules, 2023, v. 28, n. 18, p. 6511, doi. 10.3390/molecules28186511
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- Article
Innenrücktitelbild: Expeditious Access to Morphinans by Chemical Synthesis (Angew. Chem. 27/2022).
- Published in:
- Angewandte Chemie, 2022, v. 134, n. 27, p. 1, doi. 10.1002/ange.202207234
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- Article
Expeditious Access to Morphinans by Chemical Synthesis.
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- Angewandte Chemie, 2022, v. 134, n. 27, p. 1, doi. 10.1002/ange.202203186
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Inside Back Cover: Expeditious Access to Morphinans by Chemical Synthesis (Angew. Chem. Int. Ed. 27/2022).
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- Angewandte Chemie International Edition, 2022, v. 61, n. 27, p. 1, doi. 10.1002/anie.202207234
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- Article
Expeditious Access to Morphinans by Chemical Synthesis.
- Published in:
- Angewandte Chemie International Edition, 2022, v. 61, n. 27, p. 1, doi. 10.1002/anie.202203186
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- Article
Diversity-Oriented Synthesis of Enantiomerically Pure Steroidal Tetracycles Employing Stille/Diels-Alder Reaction Sequences.
- Published in:
- Chemistry - A European Journal, 2008, v. 14, n. 24, p. 7236, doi. 10.1002/chem.200800601
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- Article
Chemoenzymatic pathways for the synthesis of biologically active natural products.
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- Journal & Proceedings of the Royal Society of New South Wales, 2016, v. 149, n. 1/2, p. 34
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- Article
Syntheses of the (±)‐, (+)‐, and (−)‐Forms of 2‐Amino‐3‐(8‐hydroxyquinolin‐3‐yl)propanoic Acid (8HQ‐3Ala) from a Common Dehydroamino Acid Methyl Ester Precursor.
- Published in:
- Asian Journal of Organic Chemistry, 2022, v. 11, n. 4, p. 1, doi. 10.1002/ajoc.202100455
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- Article
Front Cover: The Synthesis, Structural Characterisation and Chemical Manipulation of the [6+3] Cycloadduct Derived from α‐Tropolone O‐Methyl Ether and Trimethylenemethane (Asian J. Org. Chem. 8/2019).
- Published in:
- Asian Journal of Organic Chemistry, 2019, v. 8, n. 8, p. 1141, doi. 10.1002/ajoc.201900404
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- Article
The Synthesis, Structural Characterisation and Chemical Manipulation of the [6+3] Cycloadduct Derived from α‐Tropolone O‐Methyl Ether and Trimethylenemethane.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 8, p. 1458, doi. 10.1002/ajoc.201900334
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- Article
Generation of (+)-Prezizanol, (+)-Prezizaene, and the ent-β-Isopipitzol Framework via Cationic Rearrangement of Khusiol and Related Compounds.
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- Asian Journal of Organic Chemistry, 2014, v. 3, n. 5, p. 632, doi. 10.1002/ajoc.201400019
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- Article
Cover Picture: Generation of (+)-Prezizanol, (+)-Prezizaene, and the ent-β-Isopipitzol Framework via Cationic Rearrangement of Khusiol and Related Compounds (Asian J. Org. Chem. 5/2014).
- Published in:
- Asian Journal of Organic Chemistry, 2014, v. 3, n. 5, p. 569, doi. 10.1002/ajoc.201490008
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- Article
An Eleven-Step Synthesis of Galanthamine from Commercially Available Materials.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 35, p. 5862, doi. 10.1002/ejoc.201601085
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- Article
A Total Synthesis of Galanthamine Involving De Novo Construction of the Aromatic C-Ring.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 17, p. 3771, doi. 10.1002/ejoc.201500365
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- Article
Modular Total Syntheses of Lamellarin G Trimethyl Ether and Lamellarin S.
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- European Journal of Organic Chemistry, 2011, v. 2011, n. 1, p. 88, doi. 10.1002/ejoc.201001133
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- Article
Palladium-Catalysed Cross-Coupling and Related Reactions Involving Pyrroles.
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- European Journal of Organic Chemistry, 2006, v. 2006, n. 14, p. 3043, doi. 10.1002/ejoc.200500911
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- Article
The Inhibition of RNA Viruses by Amaryllidaceae Alkaloids: Opportunities for the Development of Broad-Spectrum Anti- Coronavirus Drugs.
- Published in:
- Chemistry - An Asian Journal, 2022, v. 17, n. 4, p. 1, doi. 10.1002/asia.202101215
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- Article