Add to ORKGSyntheses of 6-epi- and 8-epi-otteliones, corresponding to earlier proposed structures of the biologically potent natural product ottelione A, have been accomplished from the readily available Diels-Alder adduct of cyclopentadiene and p-benzoquinone
Rare 4-methylenecyclohex-2-enone is prepared from a Diels-Alder methanesulfonate adduct and sodium i...
A total synthesis of the recently isolated polyketide natural product (±)-ambuic acid has been accom...
A total synthesis of the recently isolated polyketide natural product (+/-)-ambuic acid has been a...
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...
Following our recent total synthesis of the biologically potent natural products otteliones A and B ...
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...
Following our recent total synthesis of the biologically potent natural products otteliones A and B ...
A stereoselective strategy for the rapid acquisition of the complete framework (dideoxyottelione A) ...
The isolation of the two diastereomeric otteliones A and B from the widely occurring but little stud...
The intramolecular Diels-Alder adduct 12 was converted via dimesylate 20 into dienone 7, which repre...
A total synthesis of the novel, biologically active epoxyquinone natural product (\pm)-jesterone has...
A total synthesis of the novel, biologically active epoxyquinone natural product (±)-jesterone has b...
An enantioselective total synthesis of the novel, biologically active epoxyquinone natural product (...
Rare 4-methylenecyclohex-2-enone is prepared from a Diels-Alder methanesulfonate adduct and sodium i...
A total synthesis of the recently isolated polyketide natural product (±)-ambuic acid has been accom...
A total synthesis of the recently isolated polyketide natural product (+/-)-ambuic acid has been a...
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...
Following our recent total synthesis of the biologically potent natural products otteliones A and B ...
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...
Following our recent total synthesis of the biologically potent natural products otteliones A and B ...
A stereoselective strategy for the rapid acquisition of the complete framework (dideoxyottelione A) ...
The isolation of the two diastereomeric otteliones A and B from the widely occurring but little stud...
The intramolecular Diels-Alder adduct 12 was converted via dimesylate 20 into dienone 7, which repre...
A total synthesis of the novel, biologically active epoxyquinone natural product (\pm)-jesterone has...
A total synthesis of the novel, biologically active epoxyquinone natural product (±)-jesterone has b...
An enantioselective total synthesis of the novel, biologically active epoxyquinone natural product (...
Rare 4-methylenecyclohex-2-enone is prepared from a Diels-Alder methanesulfonate adduct and sodium i...
A total synthesis of the recently isolated polyketide natural product (±)-ambuic acid has been accom...
A total synthesis of the recently isolated polyketide natural product (+/-)-ambuic acid has been a...