A protective group free, concise, and stereoselective total synthesis of (+)-artemisinin, starting from readily available (R)-(+)-citronellal, is described. Asymmetric 1, 4-addition, Aldol condensation, Ene reaction, regioselective hydroboration are the key steps involved in the total synthesis of the target molecule
A strategy has been developed that culminated in a stereoselective total synthesis of the tetracycli...
A new chiral salen ligand based on two ferrocenyl groups is designed. Unlike known salen ligands, of...
A simple and efficient asymmetric total synthesis of the bis-macrolactone (-)-colletol was accomplis...
The total synthesis of the novel antimalarial drug, a sesquiterpene endoperoxide, (+)-artemisinin is...
Here, we describe an efficient and diversity-oriented entry to both (-)-artemisinin (1) and its natu...
International audienceA formal synthesis of artemisinin starting from amorphadiene is described. Thi...
A stereoselective protection-free asymmetric total synthesis of (+)-chamuvarinin (1), a potent antic...
A facile stereoselective total synthesis of secondary metabolite (+)-polyrhacitide A is described. S...
Isoxazoline analogues of artemisinin were obtained in low yield and low diastereoselectivity from th...
(+) Artemisinin is a sesquiterpene endoperoxide lactone with an unprecedented structure is a natural...
Access restricted to the OSU CommunityA flexible, convergent-divergent strategy for the asymmetric t...
We present a four-step synthesis of (+)-artemone from (–)- linalool, featuring iminium organocatalys...
A stereoselective synthesis leading to (-)-ara-cyclohexenyl-adenine is described. The synthesis star...
This thesis is concerned with the total syntheses of natural products and the development of a novel...
A highly anti-selective formal imino-aldol methodology has been developed and applied to asymmetric ...
A strategy has been developed that culminated in a stereoselective total synthesis of the tetracycli...
A new chiral salen ligand based on two ferrocenyl groups is designed. Unlike known salen ligands, of...
A simple and efficient asymmetric total synthesis of the bis-macrolactone (-)-colletol was accomplis...
The total synthesis of the novel antimalarial drug, a sesquiterpene endoperoxide, (+)-artemisinin is...
Here, we describe an efficient and diversity-oriented entry to both (-)-artemisinin (1) and its natu...
International audienceA formal synthesis of artemisinin starting from amorphadiene is described. Thi...
A stereoselective protection-free asymmetric total synthesis of (+)-chamuvarinin (1), a potent antic...
A facile stereoselective total synthesis of secondary metabolite (+)-polyrhacitide A is described. S...
Isoxazoline analogues of artemisinin were obtained in low yield and low diastereoselectivity from th...
(+) Artemisinin is a sesquiterpene endoperoxide lactone with an unprecedented structure is a natural...
Access restricted to the OSU CommunityA flexible, convergent-divergent strategy for the asymmetric t...
We present a four-step synthesis of (+)-artemone from (–)- linalool, featuring iminium organocatalys...
A stereoselective synthesis leading to (-)-ara-cyclohexenyl-adenine is described. The synthesis star...
This thesis is concerned with the total syntheses of natural products and the development of a novel...
A highly anti-selective formal imino-aldol methodology has been developed and applied to asymmetric ...
A strategy has been developed that culminated in a stereoselective total synthesis of the tetracycli...
A new chiral salen ligand based on two ferrocenyl groups is designed. Unlike known salen ligands, of...
A simple and efficient asymmetric total synthesis of the bis-macrolactone (-)-colletol was accomplis...
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