Articles citing this paper
A New Macrocyclic γ-Pyrone From a Southern Australian Marine Red Alga
L Murray, G Currie and RJ Capon
48(8) pp.1485 - 1489
23 articles found in Crossref database.
Encyclopedia of Marine Natural Products (2014)
Pd-catalysed regioselective C–H functionalisation of 2-pyrones
Burns Michael J.,
Thatcher Robert J.,
Taylor Richard J. K., Fairlamb Ian J. S.
Dalton Transactions. 2010 39(43). p.10391
Natural Products of Marine Macroalgae from South Eastern Australia, with Emphasis on the Port Phillip Bay and Heads Regions of Victoria
Lever James,
Brkljača Robert,
Kraft Gerald, Urban Sylvia
Marine Drugs. 2020 18(3). p.142
Natural and synthetic 2H-pyran-2-ones and their versatility in organic synthesis
Goel Atul, Ram Vishnu J.
Tetrahedron. 2009 65(38). p.7865
Biodiversity and Natural Product Diversity (2002)
Gold Catalysis for Heterocyclic Chemistry: A Representative Case Study on Pyrone Natural Products
Fürstner Alois
Angewandte Chemie International Edition. 2018 57(16). p.4215
Gold‐Katalyse für die Heterocyclenchemie: eine repräsentative Fallstudie zu Naturstoffen der Pyron‐Reihe
Fürstner Alois
Angewandte Chemie. 2018 130(16). p.4289
First report of substituted 2H-pyranoids from brown seaweed Turbinaria conoides with antioxidant and anti-inflammatory activities
Chakraborty Kajal, Dhara Shubhajit
Natural Product Research. 2020 34(24). p.3451
Dictionary of Natural Products (1998)
Total Synthesis of an Exceptional Brominated 4‐Pyrone Derivative of Algal Origin: An Exercise in Gold Catalysis and Alkyne Metathesis
Hoffmeister Laura,
Fukuda Tsutomu,
Pototschnig Gerit, Fürstner Alois
Chemistry – A European Journal. 2015 21(12). p.4529
Marine natural products
Faulkner D. John
Natural Product Reports. 1997 14(3). p.259
Biodiversity and Natural Product Diversity (2002)
Pyrone-derived Marine Natural Products: A Review on Isolation, Bio-activities and Synthesis
Singh Keisham S.
Current Organic Chemistry. 2020 24(4). p.354
2-Pyrone natural products and mimetics: isolation, characterisation and biological activity
McGlacken Gerard P., Fairlamb Ian J. S.
Natural Product Reports. 2005 22(3). p.369
Study towards bioactive pyrone derivatives from the marine red alga Phacelocarpus labillardieri
Song Dschun,
Blond Gaëlle, Fürstner Alois
Tetrahedron. 2003 59(35). p.6899
Ulvapyrone, a pyrone-linked benzochromene from sea lettuce Ulva lactuca Linnaeus (family Ulvaceae): newly described anti-inflammatory agent attenuates arachidonate 5-lipoxygenase
Chakraborty Kajal,
Dhara Shubhajit, Mani Aswathy Elizabeth
Natural Product Research. 2022 36(16). p.4114
Total Synthesis of Neurymenolide A Based on a Gold‐Catalyzed Synthesis of 4‐Hydroxy‐2‐pyrones
Chaładaj Wojciech,
Corbet Matthieu, Fürstner Alois
Angewandte Chemie. 2012 124(28). p.7035
Gold‐ or Silver‐Catalyzed Syntheses of Pyrones and Pyridine Derivatives: Mechanistic and Synthetic Aspects
Preindl Johannes,
Jouvin Kévin,
Laurich Daniel,
Seidel Günter, Fürstner Alois
Chemistry – A European Journal. 2016 22(1). p.237
Total Synthesis of Neurymenolide A Based on a Gold‐Catalyzed Synthesis of 4‐Hydroxy‐2‐pyrones
Chaładaj Wojciech,
Corbet Matthieu, Fürstner Alois
Angewandte Chemie International Edition. 2012 51(28). p.6929
Potential products from the highly diverse and endemic macroalgae of Southern Australia and pathways for their sustainable production
Lorbeer A. J.,
Tham R., Zhang W.
Journal of Applied Phycology. 2013 25(3). p.717
Total Synthesis and Stereochemical Revision of Phacelocarpus 2‐Pyrone A
Ronson Thomas O.,
Burns Michael J.,
Voelkel Martin H. H.,
Evans Kieren J.,
Lynam Jason M.,
Taylor Richard J. K., Fairlamb Ian J. S.
Chemistry – A European Journal. 2015 21(52). p.18905
Gold catalysis in total synthesis – recent achievements
Pflästerer Daniel, Hashmi A. Stephen K.
Chemical Society Reviews. 2016 45(5). p.1331
Identification and enhancing production of a novel macrolide compound in engineered Streptomyces peucetius
Pham Van Thuy Thi,
Nguyen Hue Thi,
Nguyen Chung Thanh,
Choi Ye Seul,
Dhakal Dipesh,
Kim Tae-Su,
Jung Hye Jin,
Yamaguchi Tokutaro, Sohng Jae Kyung
RSC Advances. 2021 11(5). p.3168
