Cyano-borrowing reaction: nickel-catalyzed direct conversion of cyanohydrins and aldehydes/ketones to β-cyano ketone
A direct nickel-catalyzed, high atom- and step-economical reaction of cyanohydrins with aldehydes or ketones via an unprecedented "cyano-borrowing reaction" has been developed. Cleavage of the C-CN bond of cyanohydrins followed by aldol condensation and conjugate addition of cyanide to α,β...
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Veröffentlicht in: | Chemical science (Cambridge) 2019-06, Vol.1 (22), p.5787-5792 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A direct nickel-catalyzed, high atom- and step-economical reaction of cyanohydrins with aldehydes or ketones
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an unprecedented "cyano-borrowing reaction" has been developed. Cleavage of the C-CN bond of cyanohydrins followed by aldol condensation and conjugate addition of cyanide to α,β-unsaturated ketones proceeded to deliver a range of racemic β-cyano ketones with good to high yields. The practical procedure with the use of a commercial and less-toxic CN source bodes well for wide application of this protocol.
A direct nickel-catalyzed, high atom- and step-economical reaction of cyanohydrins with aldehydes or ketones
via
an unprecedented "cyano-borrowing reaction" has been developed. |
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ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/c9sc00640k |