Ring-opening of chiral N-(3,4-dihydro-4-oxoquinazolin-3-yl)-substituted aziridines (Q∗-substituted aziridines): access to Q∗-free chirons
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Aziridination by oxidative addition of -aminoquinazolones to alkenes: Evidence for non-involvement of -nitrenes
2. Reagent- and chelation-controlled diastereoselective aziridination of electron-rich alkenes by 3-acetoxyamino-2-(1-hydroxy-2,2-dimethylprop-1-yl)-quinazolin-4(3H)-one
3. Desilylative elimination of the quinazolinone ring from 1-(4-oxoquinazolin-3-yl)-2-silylaziridines; preparation of an N–H aziridine in high enantiomeric excess by in situ nucleophilic addition to the derived azirine
4. Chiral aziridination of α,β-unsaturated esters and ketones using N-nitrenes in the presence of trifluoroacetic acid
5. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations
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3. A convenient synthesis of chiral vinyl aziridines via aza-Barbier–Darzen type reaction;Tetrahedron Letters;2013-07
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