A new chiral synthesis of (+)-rubiginone B2 is reported. The intramolecular cobalt-mediated [2+2+2]-cycloaddition of a triyne precursor, synthesized from (+)-citronellal, afforded a chiral anthracene, which led after a two-step oxidation to the angucyclinone antibiotic
5,8-Diacetoxy-2-acetyl-3,4-dihydronaphthalene, prepared by a new route from the Diels–Alder adduct o...
The (–)-(R)-dienone (13) was prepared in 10 steps from the known 8-hydroxy-5-methoxy-2, 3-dihydronap...
Inhibition of the ST AT3: ST AT3 protein-protein interaction is an attractive approach for cancer th...
A concise and highly enantioselective route has been developed for the synthesis of angucyclinone-ty...
A general method for the synthesis of benz[a]anthraquinones is reported. The key step is a catalytic...
A stereoselective total synthesis of the natural antibiotic (-)-8-O-methyltetrangomycin 1 is reporte...
A unified strategy for the syntheses of angucyclinone antibiotics was developed utilizing sequential...
A simple and efficient strategy for angucyclinone antibiotics is described with the disclosure of f...
A unified strategy for the syntheses of angucyclinone antibiotics was developed utilizing sequential...
The cobalt mediated [2+2+2]-cycloaddition of enediynes 13 and 18 affords linear annelated polycycles...
The total syntheses of rubiginone A<sub>2</sub>, C<sub>2</sub> and fujianmycin A are described. The ...
Rubriflordilactones A and B are highly oxygenated nortriterpenoid natural products isolated from Sc...
This thesis consists of five sections. The first four discuss chemistry that is relevant to a total ...
The PhD project started with investigation of the 1,3-dipolar cycloadditions of pyrylim ylides with ...
The importance of the anthracycline antibiotics has prompted numerous synthetic efforts toward the d...
5,8-Diacetoxy-2-acetyl-3,4-dihydronaphthalene, prepared by a new route from the Diels–Alder adduct o...
The (–)-(R)-dienone (13) was prepared in 10 steps from the known 8-hydroxy-5-methoxy-2, 3-dihydronap...
Inhibition of the ST AT3: ST AT3 protein-protein interaction is an attractive approach for cancer th...
A concise and highly enantioselective route has been developed for the synthesis of angucyclinone-ty...
A general method for the synthesis of benz[a]anthraquinones is reported. The key step is a catalytic...
A stereoselective total synthesis of the natural antibiotic (-)-8-O-methyltetrangomycin 1 is reporte...
A unified strategy for the syntheses of angucyclinone antibiotics was developed utilizing sequential...
A simple and efficient strategy for angucyclinone antibiotics is described with the disclosure of f...
A unified strategy for the syntheses of angucyclinone antibiotics was developed utilizing sequential...
The cobalt mediated [2+2+2]-cycloaddition of enediynes 13 and 18 affords linear annelated polycycles...
The total syntheses of rubiginone A<sub>2</sub>, C<sub>2</sub> and fujianmycin A are described. The ...
Rubriflordilactones A and B are highly oxygenated nortriterpenoid natural products isolated from Sc...
This thesis consists of five sections. The first four discuss chemistry that is relevant to a total ...
The PhD project started with investigation of the 1,3-dipolar cycloadditions of pyrylim ylides with ...
The importance of the anthracycline antibiotics has prompted numerous synthetic efforts toward the d...
5,8-Diacetoxy-2-acetyl-3,4-dihydronaphthalene, prepared by a new route from the Diels–Alder adduct o...
The (–)-(R)-dienone (13) was prepared in 10 steps from the known 8-hydroxy-5-methoxy-2, 3-dihydronap...
Inhibition of the ST AT3: ST AT3 protein-protein interaction is an attractive approach for cancer th...
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