The baeyer-villiger reaction of strained cage compounds, 1,3-bishomocubanones, via carbocations
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Kinetics of the Baeyer-Villiger reaction of aromatic ketones with perbenzoic acid
2. Theoretical model for the Baeyer-Villiger rearrangement
3. Dimerization of strained polycyclic ketones with diazomethane
4. The Beckmann Rearrangement of Bishomocubanone Oximes
5. Baeyer-villiger oxidation via carbocations in a strained cage system
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1. Nucleophilic additions to tricyclodecadienone epoxides. The Payne rearrangement of α,β-epoxycyclopentanols contained in a rigid tricyclic system;Tetrahedron;1994-03
2. The Baeyer-VilligerOxidation of Ketones and Aldehydes;Organic Reactions;1993-02-04
3. A study of the regioselectivity of oxygen insertion in the Baeyer–Villiger oxidation of bicyclo[2.2.1]heptan-2-ones;J. Chem. Soc., Perkin Trans. 1;1991
4. The Baeyer–Villiger Reaction;Comprehensive Organic Synthesis;1991
5. Baeyer-Villiger oxidation of hexacyclo[10.2.1.02,11.04,9.04,14.09,13]pentadeca-3,10-dione systems;The Journal of Organic Chemistry;1989-06
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