## 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 βFull Textβ option. The original article is trackable v
An Efficient Asymmetric Synthesis of Tarchonanthuslactone.
β Scribed by Dieter Enders; Daniel Steinbusch
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 155 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
β¦ Synopsis
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, and the construction of the tarchonanthuslactone skeleton (IX) by an umpolung technique. -(ENDERS*,
π SIMILAR VOLUMES
An asymmetric total synthesis of Prostaglandin E 1 (5) has with the Corey CBS catalyst gave the Ο-side chain 7 with ΟΎ96% ee. Conjugate addition using the reaction with been achieved in a two-component coupling process. The chiral hydroxycyclopentenone 6 was readily available from dilithiocyanocuprat