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Enantioselective NHC-catalyzed redox [4+2]-hetero-Diels-Alder reactions using α,β-unsaturated trichloromethyl ketones as amide equivalents (dataset)
Nassilia Attaba
(Creator)
James Edward Taylor
(Creator)
Alexandra Martha Zoya Slawin
(Creator)
Andrew David Smith
(Creator)
School of Chemistry
EaSTCHEM
Biomedical Sciences Research Complex
Dataset
Overview
Projects
(2)
Research output
(1)
Research output
Research output per year
2015
2015
2015
1
Article
Research output per year
Research output per year
1 results
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(descending)
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2015
Enantioselective NHC-catalyzed redox [4+2]-hetero-Diels-Alder reactions using α,β-unsaturated trichloromethyl ketones as amide equivalents
Attaba, N., Taylor, J. E.,
Slawin, A. M. Z.
&
Smith, A. D.
,
2 Oct 2015
,
In:
The Journal of Organic Chemistry.
80
,
19
,
p. 9728–9739
Research output
:
Contribution to journal
›
Article
›
peer-review
Open Access
File
Carboxamide
100%
N-Heterocyclic Carbene
100%
Ketones
100%
Trichloromethyl(.)
100%
Hetero Diels-Alder Cycloaddition
100%