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A Rhodium(II)‐Catalyzed Formal [4+1]‐Cycloaddition toward Spirooxindole Pyrrolone Construction Employing Vinyl Isocyanates as 1,4‐Dipoles
Ist Teil von
Angewandte Chemie (International ed.), 2017-06, Vol.56 (23), p.6604-6608
Auflage
International ed. in English
Ort / Verlag
Germany: Wiley Subscription Services, Inc
Erscheinungsjahr
2017
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
A RhII‐catalyzed, formal [4+1]‐cycloaddition between diazooxindoles as electrophilic C1 synthons and 1,3‐heterodienes for the construction of spirooxindole pyrrolones is described. Employing vinyl isocyanates as 1,4‐dipoles, the cycloannulation occurs under relatively mild conditions and provides the corresponding pyrrolones in good to excellent yields.
Put a ring on it: The title reaction between diazooxindoles as electrophilic C1 synthons and 1,3‐heterodienes enables the construction of spirooxindole pyrrolones. Employing vinyl isocyanates as 1,4‐dipoles, the cycloannulation occurs under relatively mild conditions and provides the corresponding pyrrolones in good to excellent yields.