Publication | Closed Access
Diastereoselective Synthesis of Functionalized Tetrahydrocarbazoles via a Domino-Ring Opening–Cyclization of Donor–Acceptor Cyclopropanes with Substituted 2-Vinylindoles
95
Citations
54
References
2014
Year
Indole-substituted Alkylidene MalonateExcellent DiastereoselectivityEngineeringHeterocyclicNovel OrganocatalystsNatural SciencesDiversity-oriented SynthesisSubstituted 2-VinylindolesOrganic ChemistryCis AlignmentDomino-ring Opening–cyclizationChemistryHeterocycle ChemistryFunctionalized TetrahydrocarbazolesSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
A new domino synthetic approach for the synthesis of highly functionalized tetrahydrocarbazoles via DROC of various functionalized DA-cyclopropanes with 2-indolylnitroethylene and indole-substituted alkylidene malonate is described. The tetrahydrocarbazoles were obtained with excellent diastereoselectivity having cis alignment of the 1,4-appendages across the six-membered carbocyclic ring.
| Year | Citations | |
|---|---|---|
Page 1
Page 1