Asymmetric Robinson Annulation of 3‑Indolinone-2-carboxylates with Cyclohexenone: Access to Chiral Bridged Tricyclic Hydrocarbazoles

A chiral bifuntional thiourea catalyzed diastereo- and enantioselective Michael addition followed by an intramolecular Aldol reaction of 3-indolinone-2-carboxylates with cyclohexenone has been accomplished using a chiral thiourea catalyst. It is a novel strategy for the construction of chiral bridge...

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Veröffentlicht in:Organic letters 2018-07, Vol.20 (14), p.4195-4199
Hauptverfasser: Yarlagadda, Suresh, Sankaram, G. S, Balasubramanian, Sridhar, Subba Reddy, B. Venkata
Format: Artikel
Sprache:eng
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Zusammenfassung:A chiral bifuntional thiourea catalyzed diastereo- and enantioselective Michael addition followed by an intramolecular Aldol reaction of 3-indolinone-2-carboxylates with cyclohexenone has been accomplished using a chiral thiourea catalyst. It is a novel strategy for the construction of chiral bridged tricyclic hydrocarbazole derivatives bearing four contiguous stereocenters with excellent diastereo- and enantioselectivity.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.8b01575