Base hydrolysis of halolactones in the bicyclo(2.2.1)heptyl and bicyclo(2.2.2)octyl systems
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference33 articles.
1. Base hydrolysis of halolactones. The mechanism of ketone formation in the bicyclo (2,2,1) heptyl system
2. Über innermolekulare Umlagerungen in der Bicyclo‐[1.2.2]‐heptan‐Reihe, IX: Zur Kenntnis der bei der Hydratisierung von Bicyclo‐[1.2.2]‐hepten‐carbonsäuren entstehenden Lactone
3. Structure of the iodo-lactone derived from norborn-5-ene-2--carboxylic acid
4. Über innermolekulare Umlagerungen in der Bicyclo‐[1.2.2]‐heptan‐Reihe, VII. Synthese und Hydratisierung zweier stereoisomerer 2.3‐Dimethyl‐bicyclo‐[1.2.2]‐hepten‐(5)‐carbonsäuren‐(2)
5. Über innermolekulare Umlagerungen in der Bicyclo‐[1.2.2]‐heptan‐Reihe, VIII. Die Hydratisierung der beiden stereoisomeren trans ‐3‐Methyl‐bicyclo‐[1.2.2]‐hepten‐(5)‐carbonsäuren‐(2)
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2. Some Stereochemical Aspects of the Strecker Synthesis and the Bucherer - Bergs Reaction;Australian Journal of Chemistry;2004
3. Parallel solution-phase syntheses of functionalised bicyclo[2.2.2]octanes: generation of a library using orchestrated multi-step sequences of polymer-supported reagents and sequesterants;Journal of the Chemical Society, Perkin Transactions 1;2000
4. Bicyclo[2.2.2]octane-2,5-carbolactone;Australian Journal of Chemistry;1984
5. 1H and13C NMR study of the effects exerted by an oxirane ring in the epoxybicyclo-[2.2.2]octane series;Organic Magnetic Resonance;1981-10
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