Enantioselective synthesis of 20(S)-camptothecin using sharpless catalytic asymmetric dihydroxylation
β Scribed by Sang-sup Jew; Kwang-dae Ok; Hee-jin Kim; Myoung Goo Kim; Jong Min Kim; Jeong Mi Hah; Youn-sang Cho
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 218 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0957-4166
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
A novel and efficient asymmetric route to CP-734432, a lactam analog of PGE2, that shows selective agonism against the EP4 receptor subtype, is reported herein. The key steps include a Heck coupling to introduce the aryl ring at C-16 and a highly diastereoselective Sharpless asymmetric dihydroxylati
An Efficient Synthesis of (-)-Pestalotin and Its Enantiomer Using Sharpless Asymmetric Dihydroxylation. -The title compound (IV), a gibberellin synergist isolated from a phytopathogenic fungus Pestaltia cryptomeriaecola, is prepared using Sharpless asymmetric dihydroxylation as the key step. A simi
## Abstract A sixβstep asymmetric total synthesis of (20__S__)βcamptothecin (**1**) has been accomplished in 25% overall yield starting from the known pyridone **3**. The key steps in this synthesis are the chemoselective Niβcatalyzed hydrogenation of 3βcyanopyridone **6** to 3βformylpyridone **7**