The synthesis of a tricyclic marine alkaloid, fasicularin, was accomplished. Stereoselective synthesis of the aza-spirocyclic BC-ring precursor and ensuing construction of the A-ring with stereocontrolled installation of the C2 hexyl group feature prominently in the synthesis.Ministry of Education (MOE)Nanyang Technological UniversityAccepted versionThis work was supported by funding from Nanyang Technological University and the Singapore Ministry of Education and Singapore Ministry of Education (Academic Research Fund Tier 1: RG4/13)
Chapter One. Anthecularin is a new antimalarial sesquiterpene lactone, which was iso-lated from Ant...
(Chemical Equation Presented) The first total synthesis of a molecule possessing the stereochemistry...
The first synthesis of siphonodictidine and a formal synthesis of pleraplysillin-2 have been accompl...
The synthesis of a tricyclic marine alkaloid, fasicularin, was accomplished. Stereoselective synthes...
This thesis is divided into four chapters. The first chapter comprises an introduction to the fasicu...
The asymmetric total synthesis of fasicularin is reported. The key to success is the use of a chiral...
Cylindricines, lepadiformines, and fasicularin are tricyclic marine alkaloids bearing perhydropyrrol...
The first stereoselective total synthesis of (3R,8S)-falcarindiol (1) from L-tartaric acid and D-xyl...
The total synthesis of the polyacetylenic compound falcarindiol was achieved by two different routes...
Marine tricyclic alkaloids lepadiformine and fasicularin, with a unique perhydropyrrolo[2,1-j]quin...
Semipinacol rearrangements forming 1-azaspirocycles as well as a formal synthesis of fasicularin are...
Marine natural products have long served as promising compounds and scaffolds for new therapeutic ag...
This thesis is concerned with the total syntheses of natural products and the development of a novel...
Accessing natural products via de novo synthetic methods is important for the discovery of new medic...
The diastereoselective synthesis of the A-B-C tricyclic ring structure of the Stemona alkaloid stemo...
Chapter One. Anthecularin is a new antimalarial sesquiterpene lactone, which was iso-lated from Ant...
(Chemical Equation Presented) The first total synthesis of a molecule possessing the stereochemistry...
The first synthesis of siphonodictidine and a formal synthesis of pleraplysillin-2 have been accompl...
The synthesis of a tricyclic marine alkaloid, fasicularin, was accomplished. Stereoselective synthes...
This thesis is divided into four chapters. The first chapter comprises an introduction to the fasicu...
The asymmetric total synthesis of fasicularin is reported. The key to success is the use of a chiral...
Cylindricines, lepadiformines, and fasicularin are tricyclic marine alkaloids bearing perhydropyrrol...
The first stereoselective total synthesis of (3R,8S)-falcarindiol (1) from L-tartaric acid and D-xyl...
The total synthesis of the polyacetylenic compound falcarindiol was achieved by two different routes...
Marine tricyclic alkaloids lepadiformine and fasicularin, with a unique perhydropyrrolo[2,1-j]quin...
Semipinacol rearrangements forming 1-azaspirocycles as well as a formal synthesis of fasicularin are...
Marine natural products have long served as promising compounds and scaffolds for new therapeutic ag...
This thesis is concerned with the total syntheses of natural products and the development of a novel...
Accessing natural products via de novo synthetic methods is important for the discovery of new medic...
The diastereoselective synthesis of the A-B-C tricyclic ring structure of the Stemona alkaloid stemo...
Chapter One. Anthecularin is a new antimalarial sesquiterpene lactone, which was iso-lated from Ant...
(Chemical Equation Presented) The first total synthesis of a molecule possessing the stereochemistry...
The first synthesis of siphonodictidine and a formal synthesis of pleraplysillin-2 have been accompl...