Steric control of reactivity: formation of oximes, benzodiazepinone N-oxides and isoxazoloquinolinones
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1998/P2/A707857I
Reference20 articles.
1. The synthesis of 1,2,7,11b-Tetrahydroisoxazolo[2,3-d][1,4]benzodiazepin-6(5H)-ones and 1,3,3a,9b-tetrahydroisoxazolo[4,3-c]quinolin-4(5H)-ones
2. Rules for ring closure
3. X = Y - ZH systems as potential 1,3-dipoles part 35. Generation of nitrones from oximes. Class 3 processes. Tandem intramolecular michael addition (1,3-azaprotio cyclotransfer) - intermolecular 1,3-dipolar cycloaddition reactions.
4. X=Y-ZH systems as potential 1,3-dipoles. Part 31. Generation of nitrones from oximes. Background and scope of the tandem 1,2-prototropy-intramolecular cycloaddition sequence.
5. Reactions at high pressures. [3+2] Dipolar cycloaddition of nitrones with vinyl ethers
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4. ChemInform Abstract: Steric Control of Reactivity: Formation of Oximes, Benzodiazepinone N-Oxides and Isoxazoloquinolinones.;ChemInform;2010-06-20
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