Novel steric factors operating on the baeyer-villiger oxidation of bicyclo[3,3,1]Nonan-3-one system
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
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1. Different routes for the construction of biologically active diversely functionalized bicyclo[3.3.1]nonanes: an exploration of new perspectives for anticancer chemotherapeutics;RSC Advances;2023
2. Chiral bicyclic keto lactones: determination of the absolute configuration by the study of chiroptical properties and chemical correlation;Tetrahedron: Asymmetry;2004-08
3. Tandem Beckmann and Huisgen–White rearrangement as an alternative to the Baeyer–Villiger oxidation of the bicyclo[3.3.1]nonane system: first asymmetric synthesis of (–)-dihydropalustramic acid. X-Ray molecular structure of 2β-ethyl-9-phenylsulfonyl-9-azabicyclo[3.3.1]nonan-3-one;J. Chem. Soc., Perkin Trans. 1;1996
4. Asymmetric Construction of Versatile Chiral Building Blocks and their Application to the Syntheses of Natural Products;Stereoselective Synthesis (Part I) - Studies in Natural Products Chemistry;1994
5. Oxygen insertion reactions of bridged bicyclic ketones;Tetrahedron;1981-01
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