Organic Letters
Letter
Myerson, A.; Revalor, E. M.; Snead, D. R.; Stelzer, T.;
Weeranoppanant, N.; Wong, S. Y.; Zhang, P. Science 2016, 352, 61.
(8) (a) Hartwig, J.; Metternich, J. B.; Nikbin, N.; Kirschning, A.; Ley,
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(10) Hafner, A.; Filipponi, P.; Piccioni, L.; Meisenbach, M.; Schenkel,
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(11) Bal’on, Y. G.; Shul’man, M. D.; Kuznetsov, N. V. Zh. Org. Chem.
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(12) (a) Matteson, D. S.; Man, H.-W.; Ho, O. C. J. Am. Chem. Soc.
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(13) For example, see: (a) Stymiest, J. L.; Bagutski, V.; French, R. M.;
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Nature 2014, 513, 183.
enhances the synthetic utility of DCMLi in organic synthesis
and appeals attractive to the scientific community.
ASSOCIATED CONTENT
* Supporting Information
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S
The Supporting Information is available free of charge on the
Detailed experimental procedures and spectral data for
AUTHOR INFORMATION
Corresponding Authors
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ORCID
Notes
The authors declare no competing financial interest.
ACKNOWLEDGMENTS
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We are thankful for the support of the Novartis Continuous
Manufacturing Unit. In particular, we thank Dr. Helen
Lightfoot for consultations. In addition, we thank Sebastian
Trokowski, Christine Waldraff, and Stephane Schmitt for
analytical and technical support.
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