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Method for Accessing Nitrogen-Containing, B-Heteroaryl-Substituted 2,1-Borazaronaphthalenes.

ABSTRACT: The azaborine motif provides a mimic of aromatic systems through replacement of a C?C bond with a B-N bond. In particular, 2,1-borazaronaphthalenes, accessible through robust methods of synthesis and subsequent functionalization, afford an ideal platform to use for a variety of applications. However, the scope of substructures for this archetype has been limited by the lack of nitrogen-containing heteroaryls that can be incorporated within them. In this study, modified reaction conditions were developed to provide access to a wider range of substructures.

SUBMITTER: Davies GH

PROVIDER: S-EPMC5224235 | biostudies-literature | 2017 Jan

REPOSITORIES: biostudies-literature

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Method for Accessing Nitrogen-Containing, B-Heteroaryl-Substituted 2,1-Borazaronaphthalenes.

Davies Geraint H M GH Zhou Zhao-Zhao ZZ Jouffroy Matthieu M Molander Gary A GA

The Journal of organic chemistry 20161214 1

The azaborine motif provides a mimic of aromatic systems through replacement of a C═C bond with a B-N bond. In particular, 2,1-borazaronaphthalenes, accessible through robust methods of synthesis and subsequent functionalization, afford an ideal platform to use for a variety of applications. However, the scope of substructures for this archetype has been limited by the lack of nitrogen-containing heteroaryls that can be incorporated within them. In this study, modified reaction conditions were d ...[more]

PMID: 27966969

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