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- W2128129644 abstract "Roaming the range: The title reaction tolerates a wide range of substituents on the resulting pyridine ring using mild reaction conditions (see scheme; esp=α,α,α′,α′-tetramethyl-1,3-benzenedipropionic acid). The formation of the key intermediate is catalyst-controlled, and subsequent cyclization and oxidation affords pyridines in excellent yields. The method has been used for the efficient synthesis of polyarylpyridines. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
- W2128129644 created "2016-06-24" @default.
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- W2128129644 date "2013-01-10" @default.
- W2128129644 modified "2023-10-02" @default.
- W2128129644 title "Synthesis of Pyridines by Carbenoid-Mediated Ring Opening of 2<i>H</i>-Azirines" @default.
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- W2128129644 doi "https://doi.org/10.1002/anie.201209301" @default.
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