A direct synthesis of stereodefined halodienes is reported. Those key building blocks enable a concise access to polyenic products, as demonstrated in a modular synthesis of Inthomycin C
A formal synthesis of crocacin C is described proving the versatility of Prins cyclization in natura...
The Matteson homologation was found to be a versatile tool for the construction of the linear polyke...
Typescript (photocopy).A highly stereoselective, convergent synthesis of ( )-trichodiene was develop...
A direct synthesis of stereodefined halodienes is reported. Those key building blocks enable a conci...
The inthomycins are a family of structurally and biologically rich natural products isolated from St...
We have reported a direct and stereoselective synthesis of functionalized dienoic carboxylates from ...
This dissertation concerns the stereoselective synthesis of optically pure compound 196, the C₁₆-C₃₂...
Strategic positioning of a silyl group on the diene unit of a diene-ene substrate allows rigorous re...
This account describes our efforts toward developing a stereodivergent entry to perophoramidine and ...
This thesis describes research towards the total syntheses of two bacterial polyene natural products...
A highly stereoselective synthesis of the racemic oxatetracyclic core of platensimycin has been acco...
The intramolecular Diels-Alder reaction is widely recognized as a powerful and versatile method for ...
The diastereoselective synthesis and structural characterization of a wide range of wholly-synthetic...
An efficient and convergent synthesis of the C<sub>5</sub>–C<sub>18</sub> fragment of halichomycin i...
A short (10 step) and efficient (15% overall yield) synthesis of the natural product (−)-(3R)-inthom...
A formal synthesis of crocacin C is described proving the versatility of Prins cyclization in natura...
The Matteson homologation was found to be a versatile tool for the construction of the linear polyke...
Typescript (photocopy).A highly stereoselective, convergent synthesis of ( )-trichodiene was develop...
A direct synthesis of stereodefined halodienes is reported. Those key building blocks enable a conci...
The inthomycins are a family of structurally and biologically rich natural products isolated from St...
We have reported a direct and stereoselective synthesis of functionalized dienoic carboxylates from ...
This dissertation concerns the stereoselective synthesis of optically pure compound 196, the C₁₆-C₃₂...
Strategic positioning of a silyl group on the diene unit of a diene-ene substrate allows rigorous re...
This account describes our efforts toward developing a stereodivergent entry to perophoramidine and ...
This thesis describes research towards the total syntheses of two bacterial polyene natural products...
A highly stereoselective synthesis of the racemic oxatetracyclic core of platensimycin has been acco...
The intramolecular Diels-Alder reaction is widely recognized as a powerful and versatile method for ...
The diastereoselective synthesis and structural characterization of a wide range of wholly-synthetic...
An efficient and convergent synthesis of the C<sub>5</sub>–C<sub>18</sub> fragment of halichomycin i...
A short (10 step) and efficient (15% overall yield) synthesis of the natural product (−)-(3R)-inthom...
A formal synthesis of crocacin C is described proving the versatility of Prins cyclization in natura...
The Matteson homologation was found to be a versatile tool for the construction of the linear polyke...
Typescript (photocopy).A highly stereoselective, convergent synthesis of ( )-trichodiene was develop...
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