An efficient, asymmetric synthesis of (+)-euphococcinine
โ Scribed by Mark F Mechelke; A.I Meyers
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 134 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
The enantioselective synthesis of (+)-euphococcinine (1), a homotropane alkaloid, has been achieved in ยฎve steps from bicyclic lactam 5.
๐ SIMILAR VOLUMES
2004 Other bioactive products ## Other bioactive products U 1300 An Efficient Asymmetric Synthesis of Tarchonanthuslactone. -Key steps of the new asymmetric synthesis of tarchonanthuslactone (X) are the enzymatic transformation of diketo ester (I) to lactone (II) in excellent stereoselectivity,
An asymmetric total synthesis of Prostaglandin E 1 (5) has with the Corey CBS catalyst gave the ฯ-side chain 7 with ฯพ96% ee. Conjugate addition using the reaction with been achieved in a two-component coupling process. The chiral hydroxycyclopentenone 6 was readily available from dilithiocyanocuprat