The first total synthesis of the biologically significant bis-indole alkaloid dragmacidin D (5) has been achieved. Thermal and electronic modulation provides the key for a series of palladium-catalyzed Suzuki cross-coupling reactions that furnished the core structure of the complex guanidine- and aminoimidazole-containing dragmacidins. Following this crucial sequence, a succession of meticulously controlled final events was developed leading to the completion of the natural product
The first asymmetric total synthesis of the bis-indole marine alkaloid (+)-dragmacidin D (<b>1</b>) ...
The first total synthesis of the novel glycosylated tetrahydroisoquinoline antitumor antibiotic (−)-...
The first total syntheses of (−)-trichorabdal A and (−)-longikaurin E are reported. A unified synthe...
The first total synthesis of the biologically significant bis-indole alkaloid dragmacidin D (5) has ...
The first total synthesis of (+)-dragmacidin F has been accomplished, establishing the absolute conf...
The dragmacidins are an emerging class of bis(indole) natural products isolated from deep-water mari...
Dragmacidin D, an emerging biologically active marine natural product, has attracted attention as a ...
This review describes recent developments from our laboratory involving the synthesis of the structu...
The one-pot synthesis of three dragmacidin derivatives is reported. Sarcosine anhydride (4) is bromi...
The first asymmetric total synthesis of the bis-indole marine alkaloid (+)-dragmacidin D (1) has bee...
The first asymmetric total synthesis of the bis-indole marine alkaloid (+)-dragmacidin D (1) has bee...
Graduation date: 2007Studies toward the total syntheses of highly potent cytotoxic alkaloids\ud incl...
(+)-Stephadiamine is an unusual alkaloid isolated from the vine Stephania japonica. It features a no...
Synthetic studies towards the total synthesis of the macrocyclic marine alkaloid ‘upenamide (I) are ...
We developed a novel synthetic method of the core structure of dragmacidin E bearing a 7-membered ri...
The first asymmetric total synthesis of the bis-indole marine alkaloid (+)-dragmacidin D (<b>1</b>) ...
The first total synthesis of the novel glycosylated tetrahydroisoquinoline antitumor antibiotic (−)-...
The first total syntheses of (−)-trichorabdal A and (−)-longikaurin E are reported. A unified synthe...
The first total synthesis of the biologically significant bis-indole alkaloid dragmacidin D (5) has ...
The first total synthesis of (+)-dragmacidin F has been accomplished, establishing the absolute conf...
The dragmacidins are an emerging class of bis(indole) natural products isolated from deep-water mari...
Dragmacidin D, an emerging biologically active marine natural product, has attracted attention as a ...
This review describes recent developments from our laboratory involving the synthesis of the structu...
The one-pot synthesis of three dragmacidin derivatives is reported. Sarcosine anhydride (4) is bromi...
The first asymmetric total synthesis of the bis-indole marine alkaloid (+)-dragmacidin D (1) has bee...
The first asymmetric total synthesis of the bis-indole marine alkaloid (+)-dragmacidin D (1) has bee...
Graduation date: 2007Studies toward the total syntheses of highly potent cytotoxic alkaloids\ud incl...
(+)-Stephadiamine is an unusual alkaloid isolated from the vine Stephania japonica. It features a no...
Synthetic studies towards the total synthesis of the macrocyclic marine alkaloid ‘upenamide (I) are ...
We developed a novel synthetic method of the core structure of dragmacidin E bearing a 7-membered ri...
The first asymmetric total synthesis of the bis-indole marine alkaloid (+)-dragmacidin D (<b>1</b>) ...
The first total synthesis of the novel glycosylated tetrahydroisoquinoline antitumor antibiotic (−)-...
The first total syntheses of (−)-trichorabdal A and (−)-longikaurin E are reported. A unified synthe...