Add to ORKGPreparation of the polycyclic core of the cytotoxic natural product salvileucalin B is described. The key feature of this synthetic strategy is a copper-catalyzed intramolecular arene cyclopropanation to provide the central norcaradiene. These studies lay the foundation for continued investigations toward an enantioselective total synthesis of 1
Ineleganolide, horiolide, kavaranolide, sinulochmodin C, scabrolide A, scabrolide B, and yonarolide ...
The preparation of complex molecules (e.g., biologically active secondary metabolites) remains an im...
Salvinorin A is the active compound in the plant Salvia divinorum, commonly known as salvia. It is ...
An enantioselective total synthesis of the diterpenoid natural product (+)-salvileucalin B is repo...
The work described in this Thesis was directed towards establishing a total synthesis of the cyclopr...
Herein, we report our progress toward the total synthesis of salvadione-A, a structurally complex tr...
Copyright © ARKAT USA, Inc The document attached has been archived with permission from the publishe...
An enantioselective and diastereoselective approach toward the synthesis of the tetracyclic scaffold...
Transformations that selectively modify the furan ring present in a variety of naturals products wou...
An enantioselective and diastereoselective approach toward the synthesis of the polycyclic norditerp...
La salvinorine A est un néoclérodane naturel possédant une forte affinité pour les récepteurs opioïd...
Buchner and Curtius first reported the cyclopropanation of arenes in 1885. Since the initial discove...
The Annonaceous acetogenin cis-sylvaticin (3.12) displays potent antitumour activity. Using permanga...
Since the initial report by Diels and Alder in 1928, the [4+2] cycloaddition remains one of the most...
The Cope rearrangement of gem-dimethyl-substituted divinylcyclopropanes has been used to construct f...
Ineleganolide, horiolide, kavaranolide, sinulochmodin C, scabrolide A, scabrolide B, and yonarolide ...
The preparation of complex molecules (e.g., biologically active secondary metabolites) remains an im...
Salvinorin A is the active compound in the plant Salvia divinorum, commonly known as salvia. It is ...
An enantioselective total synthesis of the diterpenoid natural product (+)-salvileucalin B is repo...
The work described in this Thesis was directed towards establishing a total synthesis of the cyclopr...
Herein, we report our progress toward the total synthesis of salvadione-A, a structurally complex tr...
Copyright © ARKAT USA, Inc The document attached has been archived with permission from the publishe...
An enantioselective and diastereoselective approach toward the synthesis of the tetracyclic scaffold...
Transformations that selectively modify the furan ring present in a variety of naturals products wou...
An enantioselective and diastereoselective approach toward the synthesis of the polycyclic norditerp...
La salvinorine A est un néoclérodane naturel possédant une forte affinité pour les récepteurs opioïd...
Buchner and Curtius first reported the cyclopropanation of arenes in 1885. Since the initial discove...
The Annonaceous acetogenin cis-sylvaticin (3.12) displays potent antitumour activity. Using permanga...
Since the initial report by Diels and Alder in 1928, the [4+2] cycloaddition remains one of the most...
The Cope rearrangement of gem-dimethyl-substituted divinylcyclopropanes has been used to construct f...
Ineleganolide, horiolide, kavaranolide, sinulochmodin C, scabrolide A, scabrolide B, and yonarolide ...
The preparation of complex molecules (e.g., biologically active secondary metabolites) remains an im...
Salvinorin A is the active compound in the plant Salvia divinorum, commonly known as salvia. It is ...