Prof. Johan Winne received his MSc in chemistry in 2000 at Ghent University, where he also obtained his PhD degree in 2007, having studied cationic polyene cyclisations under the guidance of Prof. Pierre De Clercq. He then spent two years as a postdoctoral research fellow with Prof. Gerry Pattenden in the University of Nottingham (UK), working on the total synthesis of terpenoid natural products. In 2009, he was appointed as a doctor-assistant (30% teaching position) at Ghent University, where he acquired an independent position in 2013, and in october 2015, he was appointed as a full time independent faculty member (tenure track docent). His research interests are in organic synthesis, ranging from architecturally complex natural products, to functional and modular molecular building blocks for material science and biology research.
Stereoselective synthesis of odd-membered carbocycles via sulfur-stabilized allyl cation cycloaddition and its application in natural product
Spicing up terpenes : rapid chemical assembly approaches and aza-analoging of evolutionary conserved ent-kauranoid scaffolds
A Tale of Terpenes: modular synthesis strategies for natural cycloheptanoid scaffolds via cationic (4+3) cycloadditions
The private life of small molecules : elucidating their molecular mechanisms in plants and in cycloadditions
Copromotor: prof. Madder
Concise and modular synthesis of natural product scaffolds by heterocycle-mediated cationic cycloaddition reactions
Copromotor: Kurt Hoogewijs
Total synthesis of biologically active polycyclid terpenoids: frondosanes, liphaganes, guaianolides, zizaanes and calcitriols
Copromotor: prof. De Clercq
Heterocycle-tethered polyene cascade cyclisation towards bicyclic natural product scaffolds
Synthesis of TTX inspired guanidine scaffolds via cationic cascade cyclizations
Synthetic and Catalytic Study of Novel Stereosecelctive Vinylcyclopropanations
Novel synthesis of azulene-type dyes
Exploring the 5,6-dihydro-1,4-dithiin heterocycle in dearomative cycloadditions
Synthesis of spirocyclic alkaloid scaffolds via tandem olefination and cyclopent-annulation of (hetero)cyclic ketones
Rapid aza-analoging of common carbocyclic scaffolds via Diels-Alder/retro-Diels-Alder approach
Non-photochemical (2+2) cycloadditions for the assembly and decoration of common plant metabolite scaffolds
Dearomative cycloadditions on indoles and a formal synthesis of phalarine
Tandem functionalization of dienes as a rapid entry into N-heterocyclic scaffolds
Novel cyclopentannulations: investigating the synthetic utility of sulfur-mediated (3+2) cycloadditions
Novel application of sulfurstabilized allyl-cation equivalents for (3+2) cycloaddition Reactions in natural product synthesis
Synthesis towards the cyathane scaffold via an intramolecular (4+3)-cycloaddition reaction
Conformational analysis of evolutionary conserved terpene-ring systems in a search for privileged new scaffolds
synthesis of the tetracyclic kaurane-type diterpene scaffold using an intramolecular (4+3) cycloaddition reaction
The enantioselective synthesis of novel polycyclic scaffolds inspired on daucane sesquiterpenes using an intramolecular (4+3) cycloaddition
Natural products as inspiration for drug discovery: synthesis of the scaffold of cytotoxic guaianolides using an intramolecular (4+3) cycloaddition reaction
Synthesis of analogues of frondosin B and liphagal, formal total synthesis of frondosin B
Biomimetic drug discovery: exploration of oxidative variations of polycyclic carbon skeletons
Synthesis of building blocks for calcitriol analogues using a 6π-electrocyclisation