Nucleophilic cleavage of 2,2-dimethylaziridines: competition between SN2 and postulated “SET” mechanism.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
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2. Tandem aziridine ring opening-disulfide formation-reduction-Michael addition in one-pot mediated by tetrathiomolybdate;Tetrahedron;2015-09
3. Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions;The Journal of Organic Chemistry;2014-05-21
4. Asymmetric Substitution at the Tetrasubstituted Chiral Carbon: Catalytic Ring-Opening Alkylation of Racemic 2,2-Disubstituted Aziridines with 3-Substituted Oxindoles;Journal of the American Chemical Society;2013-12-10
5. Design and synthesis of some new C2-symmetric chiral disulfonamides from aminoacids and the application in diethyl zinc addition to benzaldehyde;Chinese Journal of Chemistry;2010-08-27
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