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Asymmetric Isothiourea-Catalysed Formal [3+2] Cycloadditions of Ammonium Enolates with Oxaziridines.

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Title: Asymmetric Isothiourea-Catalysed Formal [3+2] Cycloadditions of Ammonium Enolates with Oxaziridines.
Authors: Smith SR; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK)., Fallan C; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK)., Taylor JE; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK)., McLennan R; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK)., Daniels DS; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK)., Morrill LC; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK)., Slawin AM; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK)., Smith AD; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK). ads10@st.andrews.ac.uk.
Source: Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2015 Jul 13; Vol. 21 (29), pp. 10530-6. Date of Electronic Publication: 2015 Jun 12.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-VCH Country of Publication: Germany NLM ID: 9513783 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1521-3765 (Electronic) Linking ISSN: 09476539 NLM ISO Abbreviation: Chemistry Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Asymmetric Isothiourea-Catalysed Formal [3+2] Cycloadditions of Ammonium Enolates with Oxaziridines.
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  Data: <searchLink fieldCode="AU" term="%22Smith+SR%22">Smith SR</searchLink>; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK).<br /><searchLink fieldCode="AU" term="%22Fallan+C%22">Fallan C</searchLink>; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK).<br /><searchLink fieldCode="AU" term="%22Taylor+JE%22">Taylor JE</searchLink>; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK).<br /><searchLink fieldCode="AU" term="%22McLennan+R%22">McLennan R</searchLink>; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK).<br /><searchLink fieldCode="AU" term="%22Daniels+DS%22">Daniels DS</searchLink>; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK).<br /><searchLink fieldCode="AU" term="%22Morrill+LC%22">Morrill LC</searchLink>; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK).<br /><searchLink fieldCode="AU" term="%22Slawin+AM%22">Slawin AM</searchLink>; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK).<br /><searchLink fieldCode="AU" term="%22Smith+AD%22">Smith AD</searchLink>; EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST (UK). ads10@st.andrews.ac.uk.
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  Data: <searchLink fieldCode="JN" term="%229513783%22">Chemistry (Weinheim an der Bergstrasse, Germany)</searchLink> [Chemistry] 2015 Jul 13; Vol. 21 (29), pp. 10530-6. <i>Date of Electronic Publication: </i>2015 Jun 12.
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