1,3-Azaprotio cyclotransfer. Nitrone-forming oxime–alkyne cyclisations
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1993/C3/C39930000372
Reference9 articles.
1. 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.
2. X = Y - ZH Systems as potential 1,3-dipoles. Part 37 generation of nitrones from oximes. Tandem intramolecular 1,3-azaprotio cyclotransfer - intramolecular 1,3-dipolar cycloaddition reactions. Class 4 processes.
3. Reverse Cope eliminations. Pyrrolidine and piperidine N-oxides by intramolecular addition of N,N-disubstituted hydroxylamines to unactivated double bonds
4. Stereoselective synthesis of (.+-.)-indolizidines 167B, 205A, and 207A. Enantioselective synthesis of (-)-indolizidine 209B
5. Hydroxylamine-alkyne cyclisations. A new method for the synthesis of cyclic nitrones
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