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Synthetic efforts on the road to marine natural products bearing 4-O -2,3,4,6-tetrasubstituted THPs: an update . Marta Fariña-Ramos, Celina García, Víctor S. Martín, Sergio J. Álvarez-Méndez
, RSC Adv.
, 2021
, 11
, 5832
Recent applications of the hetero Diels–Alder reaction in the total synthesis of natural products . Majid M. Heravi, Tahereh Ahmadi, Mahdieh Ghavidel, Bahareh Heidari, Hoda Hamidi
, RSC Adv.
, 2015
, 5
, 101999
A Maitland–Japp inspired synthesis of dihydropyran-4-ones and their stereoselective conversion to functionalised tetrahydropyran-4-ones . Paul A. Clarke, Philip B. Sellars, Nadiah Mad Nasir
, Org. Biomol. Chem.
, 2015
, 13
, 4743
The modified Julia olefination: alkene synthesis via the condensation of metallated heteroarylalkylsulfones with carbonyl compounds . Paul R. Blakemore
, J. Chem. Soc., Perkin Trans. 1
, 2002
, 2563
Radicals in natural product synthesis . Kevin J. Romero, Matthew S. Galliher, Derek A. Pratt, Corey R. J. Stephenson
, Chem. Soc. Rev.
, 2018
, 47
, 7851
Skipped dienes in natural product synthesis . Greg Petruncio, Zachary Shellnutt, Synah Elahi-Mohassel, Suman Alishetty, Mikell Paige
, Nat. Prod. Rep.
, 2021
, 38
, 2187
Strategies for the construction of tetrahydropyran rings in the synthesis of natural products . Nadiah Mad Nasir, Kristaps Ermanis, Paul A. Clarke
, Org. Biomol. Chem.
, 2014
, 12
, 3323
Marine natural products . Anthony R. Carroll, Brent R. Copp, Tanja Grkovic, Robert A. Keyzers, Michèle R. Prinsep
, Nat. Prod. Rep.
, 2024
, 41
, 162
The stereodivergent formation of 2,6-cis and 2,6-trans -tetrahydropyrans: experimental and computational investigation of the mechanism of a thioester oxy-Michael cyclization . Kristaps Ermanis, Yin-Ting Hsiao, Uğur Kaya, Alan Jeuken, Paul A. Clarke
, Chem. Sci.
, 2017
, 8
, 482
Synthesis of 2,6-trans - and 3,3,6-trisubstituted tetrahydropyran-4-ones from Maitland–Japp derived 2H -dihydropyran-4-ones: a total synthesis of diospongin B . Paul A. Clarke, Nadiah Mad Nasir, Philip B. Sellars, Alejandra M. Peter, Connor A. Lawson, James L. Burroughs
, Org. Biomol. Chem.
, 2016
, 14
, 6840