N-Heterocyclic carbene-catalysed homoenolate addition reaction to 3-cyano-2-imino-2H-chromenes: synthesis of C4-functionalized 2-amino-3-cyano-4H-chromene

A diastereoselective N-heterocyclic carbene-catalysed reaction between enal and 3-cyano-2-imino-2H-chromene is described for accessing a new type of C4-functionalized 2-amino-3-cyano-4H-chromene. A wide variety of enals and iminochromenes afforded the desired homoenolate addition product 2-amino-4H-...

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Veröffentlicht in:Organic & biomolecular chemistry 2022-11, Vol.20 (42), p.8203-8208
Hauptverfasser: Pushpendra Mani Shukla, Pratap, Aniruddh, Maji, Biswajit
Format: Artikel
Sprache:eng
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Zusammenfassung:A diastereoselective N-heterocyclic carbene-catalysed reaction between enal and 3-cyano-2-imino-2H-chromene is described for accessing a new type of C4-functionalized 2-amino-3-cyano-4H-chromene. A wide variety of enals and iminochromenes afforded the desired homoenolate addition product 2-amino-4H-chromenes in good yields and with moderate to good diastereoselectivities.
ISSN:1477-0520
1477-0539
DOI:10.1039/d2ob01447e