## Abstract The benzannulated spiroketal cores (IV) of berkelic acid are readily produced by HornerโWadsworthโEmmons olefination and a oneโpot hydrogenation/deprotection/cyclization process.
ChemInform Abstract: Synthetic Approaches to [5,6]-Benzannulated Spiroketal Natural Products
โ Scribed by Michael C. McLeod; Margaret A. Brimble; Dominea C. K. Rathwell; Zoe E. Wilson; Tsz-Ying Yuen
- Book ID
- 115554277
- Publisher
- John Wiley and Sons
- Year
- 2012
- Weight
- 18 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0931-7597
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## Abstract A novel route to simple 6,5โbenzannulated spiroketal analogues has been developed. A convergent HornerโWadsworthโEmmons olefination enabled ready assembly of the spiroketal precursors. Use of a benzyl protecting group strategy enabled an efficient oneโpot hydrogenation/deprotection/spir
## 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 โFull Textโ option. The original article is trackable v