The intramolecular Diels-Alder adduct 12 was converted via dimesylate 20 into dienone 7, which represents the unusual, and apparently quite stable, core of the antitumor agent ottelione B (1)
Abstract: Various intramolecular [4 + 21 cycloaddition strategies directed toward the eventual total...
This thesis concerns the design and synthesis of compounds relevant to a new strategy for the synthe...
cis- and trans-Trikentrin A are highly substituted indoles isolated from the marine sponge Trikentri...
The intramolecular Diels-Alder adduct 12 was converted via dimesylate 20 into dienone 7, which repre...
A novel synthetic approach towards the recently reported anti-tumor and anti-tuberculor natural prod...
A novel synthetic approach towards the recently reported anti-tumor and anti-tuberculor natural prod...
Syntheses of 6-epi- and 8-epi-otteliones, corresponding to earlier proposed structures of the biolog...
Syntheses of 6-epi- and 8-epi-otteliones, corresponding to earlier proposed structures of the biolog...
A stereoselective strategy for the rapid acquisition of the complete framework (dideoxyottelione A) ...
Rare 4-methylenecyclohex-2-enone is prepared from a Diels-Alder methanesulfonate adduct and sodium i...
In the cycloaddition approach towards the synthesis of the substituted anthraquinone derivative 8 as...
Adriamycin and daunomycin are two important anticancer drugs. Their toxicity and cost have led to a ...
Cycloaddition of activated furans 10 to 4-methoxycyclopent-2-enone was unexpectedly found to take pl...
This thesis concerns the design and preparation of compounds which are relevant to a new strategy fo...
Current quinone anticancer agents such as the anthracyclines are polycyclic conjugated molecules whi...
Abstract: Various intramolecular [4 + 21 cycloaddition strategies directed toward the eventual total...
This thesis concerns the design and synthesis of compounds relevant to a new strategy for the synthe...
cis- and trans-Trikentrin A are highly substituted indoles isolated from the marine sponge Trikentri...
The intramolecular Diels-Alder adduct 12 was converted via dimesylate 20 into dienone 7, which repre...
A novel synthetic approach towards the recently reported anti-tumor and anti-tuberculor natural prod...
A novel synthetic approach towards the recently reported anti-tumor and anti-tuberculor natural prod...
Syntheses of 6-epi- and 8-epi-otteliones, corresponding to earlier proposed structures of the biolog...
Syntheses of 6-epi- and 8-epi-otteliones, corresponding to earlier proposed structures of the biolog...
A stereoselective strategy for the rapid acquisition of the complete framework (dideoxyottelione A) ...
Rare 4-methylenecyclohex-2-enone is prepared from a Diels-Alder methanesulfonate adduct and sodium i...
In the cycloaddition approach towards the synthesis of the substituted anthraquinone derivative 8 as...
Adriamycin and daunomycin are two important anticancer drugs. Their toxicity and cost have led to a ...
Cycloaddition of activated furans 10 to 4-methoxycyclopent-2-enone was unexpectedly found to take pl...
This thesis concerns the design and preparation of compounds which are relevant to a new strategy fo...
Current quinone anticancer agents such as the anthracyclines are polycyclic conjugated molecules whi...
Abstract: Various intramolecular [4 + 21 cycloaddition strategies directed toward the eventual total...
This thesis concerns the design and synthesis of compounds relevant to a new strategy for the synthe...
cis- and trans-Trikentrin A are highly substituted indoles isolated from the marine sponge Trikentri...
DOI
Add to ORKG