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Title
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Recent advances in palladium-catalyzed isocyanide insertions
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Author
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Abstract
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| Isocyanides have long been known as versatile chemical reagents in organic synthesis. Their ambivalent nature also allows them to function as a CO-substitute in palladium-catalyzed cross couplings. Over the past decades, isocyanides have emerged as practical and versatile C1 building blocks, whose inherent N-substitution allows for the rapid incorporation of nitrogeneous fragments in a wide variety of products. Recent developments in palladium catalyzed isocyanide insertion reactions have significantly expanded the scope and applicability of these imidoylative cross-couplings. This review highlights the advances made in this field over the past eight years. |
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Language
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English
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Source (journal)
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Molecules: a journal of synthetic chemistry and natural product chemistry. - Bazel
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Publication
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Bazel
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2020
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ISSN
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1420-3049
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DOI
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10.3390/MOLECULES25214906
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Volume/pages
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25
:21
(2020)
, 52 p.
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Article Reference
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4906
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ISI
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000589301100001
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Pubmed ID
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33114013
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Medium
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E-only publicatie
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Full text (Publisher's DOI)
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Full text (open access)
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