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Asymmetric synthesis of (S)-camptothecin

✍ Scribed by Akio Ejima; Hirofumi Terasawa; Masamichi Sugimori; Hiroaki Tagawa


Publisher
Elsevier Science
Year
1989
Tongue
French
Weight
119 KB
Volume
30
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES


Synthetic Studies on Camptothecins. Part
✍ Li-Peng Zhang; Yong Bao; Yun-Yan Kuang; Fen-Er Chen πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 German βš– 148 KB

## Abstract A six‐step asymmetric total synthesis of (20__S__)‐camptothecin (**1**) has been accomplished in 25% overall yield starting from the known pyridone **3**. The key steps in this synthesis are the chemoselective Ni‐catalyzed hydrogenation of 3‐cyanopyridone **6** to 3‐formylpyridone **7**

Synthesis of position-specific tritium-l
✍ Allan W. Nicholas; Mansukh C. Wani; Monroe E. Wall; John A. Kepler; George F. Ta πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 French βš– 474 KB

## Abstract The synthesis is given for three ring A tritiated camptothecin (CPT) analogs as biological probes in the study of the parent compounds which are of current widespread interest as potent anticancer agents. The strategy of catalytic tritolysis of aryl halide bonds was employed, and thus t