A Formal Total Synthesis of (Β±)-Homogynolide-B. -The key intermediate keto ketals (III) and (IV), derived from ester (I), are further converted in a separate way to the target spirolactone (XIII), the Greene's precursor of homogynolide-B. The 5-exo-dig radical cyclization of the bromo acetal (X) fo
β¦ LIBER β¦
ChemInform Abstract: Enantioselective Formal Total Synthesis of (-)-Homogynolide-A.
β Scribed by A. SRIKRISHNA; T. J. REDDY
- Book ID
- 112024531
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 35 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0931-7597
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## 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 of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
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