Perophoramidine, dehaloperophoramidine, and communesin F are structurally related alkaloids having intriguing polycyclic structures. A strategy for the synthesis of dehaloperophoramidine has been developed. In this synthesis all skeletal atoms and all functional groups required to reach the target molecule are incorporated early in the sequence. This approach led to the discovery of two novel substrate-specific domino processes, one encompassing four steps and the other comprising five steps, thus resulting in an eight-step synthesis of dehaloperophoramidine
A complementary dual carbonyl activation strategy for the synthesis of polycyclic alkaloids has been...
This thesis describes investigations directed towards developing a novel synthetic route to the natu...
The synthesis of six cyclic depsipeptoids inspired by the natural depsipeptide sansalvamide A is des...
Perophoramidine and communesin F are structurally related indole alkaloids with an intriguing polycy...
This account describes our efforts toward developing a stereodivergent entry to perophoramidine and ...
Perophoramidine and communesin F are structurally related indole alkaloids with an intriguing polycy...
The synthesis of dehaloperophoramidine, a non-halogenated derivative of the marine natural product p...
Perophoramidine 1 is a halogenated natural product which contains two contiguous quaternary centres ...
ABSTRACT: Expedient synthetic approaches to the highly functionalized polycyclic alkaloids communesi...
Expedient synthetic approaches to the highly functionalized polycyclic alkaloids communesin F and pe...
A concise approach toward the total synthesis of the communesin alkaloids and perophoramidine is rep...
Expedient synthetic approaches to the highly functionalized polycyclic alkaloids communesin F and pe...
An efficient, unified, and stereodivergent approach toward communesin F and perophoramidine was exam...
An efficient, unified, and stereodivergent approach toward communesin F and perophoramidine was exam...
Chapter one discusses previous synthetic efforts toward the communesin alkaloids and perophoramidine...
A complementary dual carbonyl activation strategy for the synthesis of polycyclic alkaloids has been...
This thesis describes investigations directed towards developing a novel synthetic route to the natu...
The synthesis of six cyclic depsipeptoids inspired by the natural depsipeptide sansalvamide A is des...
Perophoramidine and communesin F are structurally related indole alkaloids with an intriguing polycy...
This account describes our efforts toward developing a stereodivergent entry to perophoramidine and ...
Perophoramidine and communesin F are structurally related indole alkaloids with an intriguing polycy...
The synthesis of dehaloperophoramidine, a non-halogenated derivative of the marine natural product p...
Perophoramidine 1 is a halogenated natural product which contains two contiguous quaternary centres ...
ABSTRACT: Expedient synthetic approaches to the highly functionalized polycyclic alkaloids communesi...
Expedient synthetic approaches to the highly functionalized polycyclic alkaloids communesin F and pe...
A concise approach toward the total synthesis of the communesin alkaloids and perophoramidine is rep...
Expedient synthetic approaches to the highly functionalized polycyclic alkaloids communesin F and pe...
An efficient, unified, and stereodivergent approach toward communesin F and perophoramidine was exam...
An efficient, unified, and stereodivergent approach toward communesin F and perophoramidine was exam...
Chapter one discusses previous synthetic efforts toward the communesin alkaloids and perophoramidine...
A complementary dual carbonyl activation strategy for the synthesis of polycyclic alkaloids has been...
This thesis describes investigations directed towards developing a novel synthetic route to the natu...
The synthesis of six cyclic depsipeptoids inspired by the natural depsipeptide sansalvamide A is des...