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 Efficient Asymmetric Synthesis of Grenadamide.
β Scribed by Rachel Green; Matt Cheeseman; Sarah Duffill; Andy Merritt; Steven D. Bull
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 9 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
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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
## 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
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.