Iminium ion catalysis: direct comparison of imidazolidinone and diarylprolinol ether reactivity
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Acknowledgement
We thank the EPSRC for financial support and the Mass Spectrometry Service, Swansea for high-resolution spectra.
References and notes (12)
- et al.
Chem. Rev.
(2007)et al.Top. Curr. Chem.
(2010) - et al.
Aldrichim. Acta
(2006) - et al.
Angew. Chem., Int. Ed.
(2005)et al.Angew. Chem., Int. Ed.
(2005)et al.Chem. Asian J.
(2008) - et al.
Org. Lett.
(2009)et al.Helv. Chim. Acta
(2010)et al.Helv. Chim. Acta
(2009)et al.Helv. Chim. Acta
(2008) - et al.
Adv. Synth. Catal.
(2004)et al.Org. Biomol. Chem.
(2006)et al.J. Am. Chem. Soc.
(2006) - et al.
Org. Lett.
(2005)et al.Angew. Chem., Int. Ed.
(2008)et al.Angew. Chem., Int. Ed.
(2011)
There are more references available in the full text version of this article.
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