T. M. Meulemans

Publications14
h-index5
Citations91
Highly Influential Citations0
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Total Synthesis of Dihydroclerodin from (R)-(_)-Carvone
The first total synthesis of the natural enantiomer of the insect-antifeedant dihydroclerodin (1) and lupulin C (40) has been achieved starting from (R)-(−)-carvone (2). In the applied strategy, the… Expand
  • 27
Enantioselective Synthesis of Functionalised Decalones by Robinson Annulation of Substituted Cyclohexanones, Derived from R-(−)-Carvone
Abstract The copper catalysed conjugate addition of methyl magnesium iodide to cyclohexenones and trapping of the enolate as its trimethylsilyl enol ether, followed by a trityl hexachloroantimonate… Expand
  • 17
Catalytic Oxidation of Homoallylalcohols to α-Alkoxytetrahydrofurans by a Pd-Nitro Complex and Molecular Oxygen
Abstract Various homoallylalcohols were highly regioselective oxidized with molecular oxygen at the terminal carbon to afford cyclic acetals (α-alkoxytetrahydrofurans) using PdNO 2 Cl(CH 3 CN) 2 as a… Expand
  • 21
Enantioselective Synthesis of Functionalized Decalones by Robinson Annulation of Substituted Cyclohexanones, Derived from R‐(‐)‐Carvone.
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Enantioselective synthesis of highly functionalised cyclohexanones starting from R-(−)-carvone
Copper (I) catalysed conjugate addition of methylmagnesium iodide to R-(−)-carvone and trapping the enolate as its trimethylsilyl enol ether, followed by a trityl perchlorate (TrClO4) catalysed… Expand
  • 14
Catalytic oxidation of homoallylalcohols to .alpha.-alkoxytetrahydrofurans by a Pd-nitro complex and molecular oxygen
Studies towards the total synthesis of insect-antifeedant dihydroclerodin.
The total synthesis of the insect-antifeedant dihydroclerodin
The total synthesis of insect antifeedant (-)-dihydroclerodin starting from R-(-)-carvone
The first total synthesis of the natural enantiomer of the insect-antifeedant dihydroclerodin ( 1 ) and lupulin C ( 268 ) has been achieved in 18 and 17 steps respectively starting from R-(-)-carvone… Expand
Enantioselective Synthesis of Cadinanes starting from R-(-)- or S-(+)-Carvone.
A new enantioselective synthesis of cadinanes, using the Mukaiyama-Michael reaction, was developed starting from R-(−)- or S-(+)-carvone. This approach gives an easy and direct access to the cadinane… Expand
  • 8