Balanol total synthesis achieved by two groups
β Scribed by BORMAN, STU
- Book ID
- 126510956
- Publisher
- American Chemical Society
- Year
- 1994
- Tongue
- English
- Weight
- 237 KB
- Volume
- 72
- Category
- Article
- ISSN
- 0009-2347
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π SIMILAR VOLUMES
A convergent enantioselective total synthesis of the natural product (-)-balanol (1) is described. In addition to benzophenone fragment 8, key intermediates are chiral bicyclic aziridine 3 and the corresponding epoxide 4, both of which undergo highly regio-and stereoselective nucleophilic ring-openi
We have developed a novel method of assaying total free catecholamines using sulphuric acid-derivatized beads for extracting and identifying catecholamine (CA) on the surface, and assaying the peroxide produced from CA by chemiluminescence (CL). Current assay methods for CA by electrochemical determ