A six-step total synthesis of the fungicidal natural product hydroxystrobilurin A is described, utilising Stille chemistry for efficient access to the strobilurin (E,Z,E)-triene system. © 2008 Elsevier Ltd. All rights reserved.Darby G. Brooke, Jonathan C. Morri
The first total synthesis of the naturally occurring dolabellane diterpenoid, acetoxyodontoschismeno...
In this paper the applicability of the Stille-coupling reaction for the synthesis of a variety of ol...
Stilbenes are biologically active metabolites of plants that have the potential to attenuate a broad...
This thesis describes the first three total syntheses of hydroxystrobilurin A, a member of the strob...
The thesis describes synthetic studies directed towards the total synthesis of 14,15-anhydrovirgini...
Stille reaction is one of the most common, efficient and selective Pd-catalyzed cross-coupling react...
Several structural analogues of strobilurin A having general formula (E)-18, in which the methyl (E)...
Several structural analogues of strobilurin A having general formula (E)-18, in which the methyl (E)...
Transition metal-mediated carbon-carbon bond forming reactions are among the most synthetically usef...
Strobilurins from fungi are the inspiration for the creation of the β-methoxyacrylate class of agric...
The zaragozic acids/squalestatins are a family of bicyclic tricarboxylic acids, isolated from a ser...
Strobilurin is a group of natural products and their synthetic analogs have been widely used to cont...
Countless natural products of polyketide origin have an E-configured 2-methyl-but-2-en-1-ol substruc...
Strobilurin analogs in which the side chain is in a meta-relationship to the pharmacophore are activ...
The Suzuki-Miyaura coupling reaction provides a con-venient access to the carbon-carbon bond formati...
The first total synthesis of the naturally occurring dolabellane diterpenoid, acetoxyodontoschismeno...
In this paper the applicability of the Stille-coupling reaction for the synthesis of a variety of ol...
Stilbenes are biologically active metabolites of plants that have the potential to attenuate a broad...
This thesis describes the first three total syntheses of hydroxystrobilurin A, a member of the strob...
The thesis describes synthetic studies directed towards the total synthesis of 14,15-anhydrovirgini...
Stille reaction is one of the most common, efficient and selective Pd-catalyzed cross-coupling react...
Several structural analogues of strobilurin A having general formula (E)-18, in which the methyl (E)...
Several structural analogues of strobilurin A having general formula (E)-18, in which the methyl (E)...
Transition metal-mediated carbon-carbon bond forming reactions are among the most synthetically usef...
Strobilurins from fungi are the inspiration for the creation of the β-methoxyacrylate class of agric...
The zaragozic acids/squalestatins are a family of bicyclic tricarboxylic acids, isolated from a ser...
Strobilurin is a group of natural products and their synthetic analogs have been widely used to cont...
Countless natural products of polyketide origin have an E-configured 2-methyl-but-2-en-1-ol substruc...
Strobilurin analogs in which the side chain is in a meta-relationship to the pharmacophore are activ...
The Suzuki-Miyaura coupling reaction provides a con-venient access to the carbon-carbon bond formati...
The first total synthesis of the naturally occurring dolabellane diterpenoid, acetoxyodontoschismeno...
In this paper the applicability of the Stille-coupling reaction for the synthesis of a variety of ol...
Stilbenes are biologically active metabolites of plants that have the potential to attenuate a broad...
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