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  4. Tertiary Amine Promoted Aziridination: Preparation of NH-Aziridines from Aliphatic ,-Unsaturated Ketones
 
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Tertiary Amine Promoted Aziridination: Preparation of NH-Aziridines from Aliphatic ,-Unsaturated Ketones
File(s)
RDCP_Synlett_final.docx (308.13 KB)
Accepted version
Author(s)
Armstrong, A
Pullin, RDC
Scutt, JN
Type
Journal Article
Abstract
trans-NH-Aziridines were prepared from aliphatic α,β-unsaturated ketones using a tertiary amine promoted reaction via in situ generated N,N-ylides. Through use of modified conditions the reaction proved to be applicable for the diastereoselective aziridination of a range of enolisable aliphatic α,β-unsaturated ketones of varying substitution patterns.
Date Issued
2015-11-03
Date Acceptance
2015-10-09
Citation
SYNLETT, 2015, 27 (1), pp.151-155
URI
http://hdl.handle.net/10044/1/29362
DOI
https://www.dx.doi.org/10.1055/s-0035-1560583
ISSN
0936-5214
Publisher
Georg Thieme Verlag Stuttgart
Start Page
151
End Page
155
Journal / Book Title
SYNLETT
Volume
27
Issue
1
Copyright Statement
© Georg Thieme Verlag Stuttgart
Subjects
Science & Technology
Physical Sciences
Chemistry, Organic
Chemistry
aziridines
organocatalysis
enones
aminimine
ylides
stereoselective
ORGANOCATALYTIC ENANTIOSELECTIVE AZIRIDINATION
CATALYTIC ASYMMETRIC AZIRIDINATION
ALPHA,BETA-UNSATURATED ALDEHYDES
STEREOSELECTIVE-SYNTHESIS
COPPER-COMPLEXES
CYCLIC ENONES
CHALCONES
OLEFINS
Publication Status
Published
Date Publish Online
2015-11-03
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