Total Synthesis of (±)-Calanolide A
✍ Scribed by Rehder, Ken S.; Kepler, John A.
- Book ID
- 119941663
- Publisher
- Taylor and Francis Group
- Year
- 1996
- Tongue
- English
- Weight
- 543 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0039-7911
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Enantioselective total synthesis of anti HIV-1 active (+)-calanolide A was achieved by a quinine-catalyzed asymmetric intramolecular oxo-Michael addition as a key step.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
A Catalytic Enantioselective Approach to Chromans and Chromanols. A Total Synthesis of (-)-Calanolides A (IX) and B (VIII) and the Vitamin E Nucleus (XIII). -The key steps in the synthesis of the title compounds are regio-and enantioselective allylic alkylation of phenols and subsequent ring closure