• Publications
  • Influence
Enantiospecific total synthesis of aciphyllene
Enantiospecific total synthesis of the sesquiterpene aciphyllene and its three epimers have been described starting from the readily available monoterpene (R)-limonene employing an intramolecularExpand
  • 12
A rapid and efficient enantiospecific synthesis of the functionalized ABC-ring system of tetranortriterpene dumsins and their analogues
A rapid and enantiospecific synthesis of the ABC ring system of tetranortriterpene dumsin and its analogues, starting from the readily available monoterpene (R)-carvone employing two RCM reactions asExpand
  • 13
A rapid enantiospecific synthesis of the (6,6,5)-tricyclic ring system of the elisabethane diterpenes
A rapid enantiospecific stereoselective synthesis of the 6,6,5-ring system of the novel tricyclic elisabethin diterpenes, starting from (R)-carvone, employing a ROM-RCM sequence as the key step, hasExpand
  • 14
Enantiospecific approaches to bicyclic vibsanes: a ring-closing metathesis reaction-based strategy to functionalized bicyclo[4.3.1]decanes
An enantiospecific synthesis of functionalized bicyclo[4.3.1]decane, the bicyclic core system present in some bi- and tricyclic vibsane diterpenoids, for example, vibsanin E, via an RCM reaction ofExpand
  • 11
Enantioselective formal total syntheses of Clavukerin A and isoclavukerin A via a ring-closing metathesis reaction
Enantioselective formal total syntheses of the marine trisnorsesquiterpenes clavukerin A and isoclavukerin A, starting from (R)-limonene employing an RCM reaction as the key step, are described.
  • 13
Asymmetric first total syntheses and assignment of absolute configuration of oxazinin-5, oxazinin-6 and preoxazinin-7.
Asymmetric first total syntheses of the unprecedented toxins oxazinin-5, oxazinin-6 and preoxazinin-7 have been achieved from a common key intermediate 18, derived from a regiocontrolled SharplessExpand
  • 5
Enantiospecific first total synthesis and confirmation of the relative and absolute stereostructure of isocalamusenone
The enantiospecific total synthesis of two epimers of the sesquiterpene isocalamusenone has been accomplished starting from the readily available monoterpene (R)-limonene, which of the naturalExpand
  • 4
Enantiospecific Synthesis Of Guaianes And Tricyclic Ring Systems Of Elisabethins And Dumsins
One area of natural product synthesis which has been heavily investigated in the last eight decades is the total synthesis of terpenoids. Among terpenoids, the presence of a great deal ofExpand
Enantiospecific synthesis and confirmation of the relative and absolute stereostructure of 11-hydroxyguaiadienes
Enantiospecific total synthesis of two epimeric sesquiterpenes 11-hydroxyguaiadienes has been accomplished starting from the readily available monoterpene (R)-limonene, which confirmed the structureExpand
  • 2