International audienceA new entry to the synthesis of anthrapyran antibiotics has been accomplished through the synthesis of a 4H-anthra[1,2-b]pyran-4,7,12-trione model. The key step features a Diels-Alder reaction between a substituted 5-vinyl-3,4-dihydro-2H-pyran and naphthoquinone as the dienophile. The resulting tetracyclic adduct is then processed towards the targeted trione in a few steps
The (–)-(R)-dienone (13) was prepared in 10 steps from the known 8-hydroxy-5-methoxy-2, 3-dihydronap...
The three most important members of the anthracycline class of antitumor antibiotics are daunorubici...
Two synthetic approaches have been investigated for the syntheses of model angucyclinones related to...
In the cycloaddition approach towards the synthesis of the substituted anthraquinone derivative 8 as...
5,8-Diacetoxy-2-acetyl-3,4-dihydronaphthalene, prepared by a new route from the Diels–Alder adduct o...
A unified strategy for the syntheses of angucyclinone antibiotics was developed utilizing sequential...
Synthetic efforts towards anticancer anthracyclines are described (including PhD thesis investigatio...
A unified strategy for the syntheses of angucyclinone antibiotics was developed utilizing sequential...
Many natural products contain a tetramic acid (pyrrolidine-2,4-dione) ring system as an integral par...
Doxorubicin has the widest spectrum of antitumor activity of all antineoplastic agents and is the mo...
Several strategies outlining approaches to the synthesis of the heteroanthracyclinones 4-demethoxyxa...
The research in this thesis aimed to identify a common intermediate that would allow the collective ...
At present anthracycline antibiotics have proven to be the most exciting agents in cancer chemothera...
The development of a general strategy for the construction of anthracyclinones based on a Diels-Alde...
The importance of the anthracycline antibiotics has prompted numerous synthetic efforts toward the d...
The (–)-(R)-dienone (13) was prepared in 10 steps from the known 8-hydroxy-5-methoxy-2, 3-dihydronap...
The three most important members of the anthracycline class of antitumor antibiotics are daunorubici...
Two synthetic approaches have been investigated for the syntheses of model angucyclinones related to...
In the cycloaddition approach towards the synthesis of the substituted anthraquinone derivative 8 as...
5,8-Diacetoxy-2-acetyl-3,4-dihydronaphthalene, prepared by a new route from the Diels–Alder adduct o...
A unified strategy for the syntheses of angucyclinone antibiotics was developed utilizing sequential...
Synthetic efforts towards anticancer anthracyclines are described (including PhD thesis investigatio...
A unified strategy for the syntheses of angucyclinone antibiotics was developed utilizing sequential...
Many natural products contain a tetramic acid (pyrrolidine-2,4-dione) ring system as an integral par...
Doxorubicin has the widest spectrum of antitumor activity of all antineoplastic agents and is the mo...
Several strategies outlining approaches to the synthesis of the heteroanthracyclinones 4-demethoxyxa...
The research in this thesis aimed to identify a common intermediate that would allow the collective ...
At present anthracycline antibiotics have proven to be the most exciting agents in cancer chemothera...
The development of a general strategy for the construction of anthracyclinones based on a Diels-Alde...
The importance of the anthracycline antibiotics has prompted numerous synthetic efforts toward the d...
The (–)-(R)-dienone (13) was prepared in 10 steps from the known 8-hydroxy-5-methoxy-2, 3-dihydronap...
The three most important members of the anthracycline class of antitumor antibiotics are daunorubici...
Two synthetic approaches have been investigated for the syntheses of model angucyclinones related to...