Publication | Closed Access
Thermal 1,6‐Electrocyclization Reactions of Acceptor‐Substituted 2,3‐Divinyl‐1<i>H</i>‐indoles Yielding Functionalized Carbazoles
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Citations
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References
1990
Year
Chemical EngineeringNew Synthetic ProceduresEngineeringDiversity Oriented SynthesisCross-coupling ReactionWittig ProceduresThermal 1,6‐ElectrocyclizationsNatural SciencesDiversity-oriented SynthesisThermal 1,6‐ElectrocyclizationOrganic ChemistryChemistryHeterocycle ChemistrySynthetic Chemistry
Abstract Three new synthetic procedures for and thermal 1,6‐electrocyclizations of acceptor‐substituted 2,3‐divinyl‐1 H ‐indoles leading to functionalizing carbazoles are described. The scope and limitations as well as some mechanistic aspects of the methodologies are discussed. The key strategies employed include Pd(II)‐catalyzed coupling and Wittig procedures.
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