The total synthesis of aculeatins A and B is described proving the versatility of Prins cyclization in natural product synthesis. The approach is convergent and highly stereoselective. Morpholine amide coupling with an alkyne and PIFA-mediated oxidative spirocyclization were utilized as key steps
A stereoselective and convergent formal approach to Salicylihalamide A and B is achieved through our...
International audienceThe classical Prins cyclization reaction has been one of the most studied reac...
A simple and efficient asymmetric total synthesis of the bis-macrolactone (-)-colletol was accomplis...
The stereoselective total synthesis of spiroketal natural product (+)-aculeatin D and unnatural (+)-...
An efficient total synthesis of the cytotoxic spiroketal natural products aculeatin A and B is descr...
The total synthesis of a pyrone natural product obolactone has been accomplished using Prins cycliza...
A formal synthesis of crocacin C is described proving the versatility of Prins cyclization in natura...
Syntheses of xestodecalactone C and epi-sporostatin are described utilising Prins cyclisations, Mits...
A new synthetic strategy was developed for a concise total synthesis of aculeatin A as a single spir...
The total synthesis of aculeatins A, B, E and F confirming the assigned absolute configuration of re...
A highly stereoselective and convergent total synthesis of PF1163 A is described while proving the v...
A stereoselective synthesis of pironetin, a natural product which is highly immunosuppressive and sh...
Stereoselective syntheses of (−)-tetrahydrolipstatin have been achieved via two divergent approaches...
The total synthesis of (10S,12S)-10-hydroxy-12-methyl-1-oxacyclododecane-2,5-dione is described prov...
A convergent and highly stereoselective formal total synthesis of the naturally occurring, cytotoxic...
A stereoselective and convergent formal approach to Salicylihalamide A and B is achieved through our...
International audienceThe classical Prins cyclization reaction has been one of the most studied reac...
A simple and efficient asymmetric total synthesis of the bis-macrolactone (-)-colletol was accomplis...
The stereoselective total synthesis of spiroketal natural product (+)-aculeatin D and unnatural (+)-...
An efficient total synthesis of the cytotoxic spiroketal natural products aculeatin A and B is descr...
The total synthesis of a pyrone natural product obolactone has been accomplished using Prins cycliza...
A formal synthesis of crocacin C is described proving the versatility of Prins cyclization in natura...
Syntheses of xestodecalactone C and epi-sporostatin are described utilising Prins cyclisations, Mits...
A new synthetic strategy was developed for a concise total synthesis of aculeatin A as a single spir...
The total synthesis of aculeatins A, B, E and F confirming the assigned absolute configuration of re...
A highly stereoselective and convergent total synthesis of PF1163 A is described while proving the v...
A stereoselective synthesis of pironetin, a natural product which is highly immunosuppressive and sh...
Stereoselective syntheses of (−)-tetrahydrolipstatin have been achieved via two divergent approaches...
The total synthesis of (10S,12S)-10-hydroxy-12-methyl-1-oxacyclododecane-2,5-dione is described prov...
A convergent and highly stereoselective formal total synthesis of the naturally occurring, cytotoxic...
A stereoselective and convergent formal approach to Salicylihalamide A and B is achieved through our...
International audienceThe classical Prins cyclization reaction has been one of the most studied reac...
A simple and efficient asymmetric total synthesis of the bis-macrolactone (-)-colletol was accomplis...
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