Trigonoliimine B, a hexacyclic alkaloid, is synthesized in seven steps from simple starting materials. The synthesis features the use of an alpha-isocyanoacetate as a glycine template for the preparation of an alpha,alpha-disubstituted alpha-amino ester that is appropriately functionalized for the construction of C, D, and E rings. Sulfolane was found to be the solvent of choice for the unprecedented Bischler-Napieralski reaction implemented for the construction of a seven-membered ring with concurrent formation of an exo-imine function
A synthetic approach to the tricyclic sesquiterpene sulcatine G, 2, bearing a novel tricyclo$[6.2.0....
Judicious substrate design allows interruption of the classical Bischler-Napieralski reaction, provi...
The work presented in this thesis focuses on the synthesis of monoterpene indole alkaloids. The fir...
Trigonoliimine B, a hexacyclic alkaloid, is synthesized in seven steps from simple starting material...
Trigonoliimines are hexacyclic bisindole alkaloids isolated recently by Hao and co-workers. A synthe...
My PhD work started with the development of a racemic access to trigonoliimine B, an hexacyclic alka...
A full account of our concise and enantioselective total syntheses of all known (−)-trigonoliimine a...
A novel synthetic route to the hexacyclic system of trigonoliimine A was accomplished in four steps ...
A full account of our concise and enantioselective total syntheses of all known (−)-trigonoliimine a...
A convergent total synthesis of trigonoliimine C has been executed by employing three catalytic tran...
This presentation identifies the ongoing research to synthesize trigonoine B. This novel, biological...
The monomeric units, benzyltetrahydroisoquinoline, parts of the total synthesis of trilobine, are ob...
The first total synthesis of the neuroactive indole alkaloid (+/-)-alstoscholarisine A is reported. ...
Bischler-Napieralski (B-N) reaction is undoubtedly one of the most powerful methodologies in organic...
A complementary dual carbonyl activation strategy for the synthesis of polycyclic alkaloids has been...
A synthetic approach to the tricyclic sesquiterpene sulcatine G, 2, bearing a novel tricyclo$[6.2.0....
Judicious substrate design allows interruption of the classical Bischler-Napieralski reaction, provi...
The work presented in this thesis focuses on the synthesis of monoterpene indole alkaloids. The fir...
Trigonoliimine B, a hexacyclic alkaloid, is synthesized in seven steps from simple starting material...
Trigonoliimines are hexacyclic bisindole alkaloids isolated recently by Hao and co-workers. A synthe...
My PhD work started with the development of a racemic access to trigonoliimine B, an hexacyclic alka...
A full account of our concise and enantioselective total syntheses of all known (−)-trigonoliimine a...
A novel synthetic route to the hexacyclic system of trigonoliimine A was accomplished in four steps ...
A full account of our concise and enantioselective total syntheses of all known (−)-trigonoliimine a...
A convergent total synthesis of trigonoliimine C has been executed by employing three catalytic tran...
This presentation identifies the ongoing research to synthesize trigonoine B. This novel, biological...
The monomeric units, benzyltetrahydroisoquinoline, parts of the total synthesis of trilobine, are ob...
The first total synthesis of the neuroactive indole alkaloid (+/-)-alstoscholarisine A is reported. ...
Bischler-Napieralski (B-N) reaction is undoubtedly one of the most powerful methodologies in organic...
A complementary dual carbonyl activation strategy for the synthesis of polycyclic alkaloids has been...
A synthetic approach to the tricyclic sesquiterpene sulcatine G, 2, bearing a novel tricyclo$[6.2.0....
Judicious substrate design allows interruption of the classical Bischler-Napieralski reaction, provi...
The work presented in this thesis focuses on the synthesis of monoterpene indole alkaloids. The fir...