Regiospecific Reductive Cleavage of the C(2)−N Bond of Aziridines Substituted with an Electron Acceptor Mediated by Mg/MeOH
Author:
Affiliation:
1. Korea Research Institute of Chemical Technology, P.O. Box 107, Yusung, Taejeon 305-606, Korea
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9806963
Reference69 articles.
1. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations
2. Synthesis of an ethylene glycol cross-linked amino acid
3. Synthesis of .alpha.-halocinnamate esters via solvolytic rearrangement of trichloroallyl alcohols
4. Regioselective nucleophilic ring opening reactions of 2,2-disubstituted aziridines — the asymmetric synthesis of α,α-disubstituted amino acids
5. Syntheses of (S)-β-pyrazolylalanine and (S)-quisqualic acid from a serine-derived aziridine
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