author_facet Sathyamoorthi, Shyam
Banerjee, Shibdas
Du Bois, J.
Burns, Noah Z.
Zare, Richard N.
Sathyamoorthi, Shyam
Banerjee, Shibdas
Du Bois, J.
Burns, Noah Z.
Zare, Richard N.
author Sathyamoorthi, Shyam
Banerjee, Shibdas
Du Bois, J.
Burns, Noah Z.
Zare, Richard N.
spellingShingle Sathyamoorthi, Shyam
Banerjee, Shibdas
Du Bois, J.
Burns, Noah Z.
Zare, Richard N.
Chemical Science
Site-selective bromination of sp3 C–H bonds
General Chemistry
author_sort sathyamoorthi, shyam
spelling Sathyamoorthi, Shyam Banerjee, Shibdas Du Bois, J. Burns, Noah Z. Zare, Richard N. 2041-6520 2041-6539 Royal Society of Chemistry (RSC) General Chemistry http://dx.doi.org/10.1039/c7sc04611a <p>A method for converting sp<sup>3</sup> C–H to C–Br bonds using an <italic>N</italic>-methyl sulfamate directing group is described. For all sulfamates examined, bromination occurs with high selectivity at the γ-carbon, affording a predictable method for C–H bond halogenation.</p> Site-selective bromination of sp<sup>3</sup> C–H bonds Chemical Science
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title Site-selective bromination of sp3 C–H bonds
title_unstemmed Site-selective bromination of sp3 C–H bonds
title_full Site-selective bromination of sp3 C–H bonds
title_fullStr Site-selective bromination of sp3 C–H bonds
title_full_unstemmed Site-selective bromination of sp3 C–H bonds
title_short Site-selective bromination of sp3 C–H bonds
title_sort site-selective bromination of sp<sup>3</sup> c–h bonds
topic General Chemistry
url http://dx.doi.org/10.1039/c7sc04611a
publishDate 2018
physical 100-104
description <p>A method for converting sp<sup>3</sup> C–H to C–Br bonds using an <italic>N</italic>-methyl sulfamate directing group is described. For all sulfamates examined, bromination occurs with high selectivity at the γ-carbon, affording a predictable method for C–H bond halogenation.</p>
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author Sathyamoorthi, Shyam, Banerjee, Shibdas, Du Bois, J., Burns, Noah Z., Zare, Richard N.
author_facet Sathyamoorthi, Shyam, Banerjee, Shibdas, Du Bois, J., Burns, Noah Z., Zare, Richard N., Sathyamoorthi, Shyam, Banerjee, Shibdas, Du Bois, J., Burns, Noah Z., Zare, Richard N.
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description <p>A method for converting sp<sup>3</sup> C–H to C–Br bonds using an <italic>N</italic>-methyl sulfamate directing group is described. For all sulfamates examined, bromination occurs with high selectivity at the γ-carbon, affording a predictable method for C–H bond halogenation.</p>
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spelling Sathyamoorthi, Shyam Banerjee, Shibdas Du Bois, J. Burns, Noah Z. Zare, Richard N. 2041-6520 2041-6539 Royal Society of Chemistry (RSC) General Chemistry http://dx.doi.org/10.1039/c7sc04611a <p>A method for converting sp<sup>3</sup> C–H to C–Br bonds using an <italic>N</italic>-methyl sulfamate directing group is described. For all sulfamates examined, bromination occurs with high selectivity at the γ-carbon, affording a predictable method for C–H bond halogenation.</p> Site-selective bromination of sp<sup>3</sup> C–H bonds Chemical Science
spellingShingle Sathyamoorthi, Shyam, Banerjee, Shibdas, Du Bois, J., Burns, Noah Z., Zare, Richard N., Chemical Science, Site-selective bromination of sp3 C–H bonds, General Chemistry
title Site-selective bromination of sp3 C–H bonds
title_full Site-selective bromination of sp3 C–H bonds
title_fullStr Site-selective bromination of sp3 C–H bonds
title_full_unstemmed Site-selective bromination of sp3 C–H bonds
title_short Site-selective bromination of sp3 C–H bonds
title_sort site-selective bromination of sp<sup>3</sup> c–h bonds
title_unstemmed Site-selective bromination of sp3 C–H bonds
topic General Chemistry
url http://dx.doi.org/10.1039/c7sc04611a