Palladium-catalysed cyclisation of chiral carbohydrate-derived geminal diacetates
β Scribed by Cedric W. Holzapfel; Lizel Marais; Francois Toerien
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 679 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
The Pd(0) and Pd(II)-catalysed cyclisafion/functionalisation reactions of acyclic carbohydrate-derived 1, ldiacetuxy-2,7-dienΒ’ and l,l-diacctoxy-2-Β’n-7-ynΒ’ compounds ptecccded in a s~reospccific fashion to furnish chiraL multi-functionalised furanoid and cyclopontanoid products. The products contained valuable enolacctatΒ’ moieties. which can be further daborated to enable the facile entry to an array of substituted five membered ring compounds.
π SIMILAR VOLUMES
Thc palladium-catal)sed 'mctallo-cnc' cyclisation, cyclisatimVcarbon~lation. -vinylstannane coupling, and Pd(lll-catalyscd chloropalladation/carboc?clisation of l,l-diacctox?-2,7-dienc and l.l-diacetoxy-2-cn-7-Snc derivatives are described The c3clic enolacetate products could rcadil 5 be comcrted i