0000000000416778

AUTHOR

Reinhard Adam

showing 4 related works from this author

Thermal 1,6-Electrocyclization Reactions of Acceptor-Substituted 2,3-Divinyl-1H-indoles Yielding Functionalized Carbazoles

1990

Three new synthetic procedures for and thermal 1,6-electrocyclizations of acceptor-substituted 2,3-divinyl-1H-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.

Electrocyclic reactionBicyclic moleculeChemistryOrganic ChemistryBiochemistryAcceptorCatalysisInorganic ChemistryChemical couplingDrug DiscoveryWittig reactionOrganic chemistryThermal reactionPhysical and Theoretical ChemistryHelvetica Chimica Acta
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ChemInform Abstract: Synthetically Attractive Indolization Processes and Newer Methods for the Preparation of Selectively Substituted Indoles

1988

The synthetically interesting processes available for indolization reactions are discussed and illustrated in tabular form and particular emphasis is placed on the more recent methods.

ChemistryGeneral MedicineCombinatorial chemistryChemInform
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ChemInform Abstract: Thermal 1,6-Electrocyclization Reactions of Acceptor-Substituted 2,3-Divinyl-1H-indoles Yielding Functionalized Carbazoles.

1990

Three new synthetic procedures for and thermal 1,6-electrocyclizations of acceptor-substituted 2,3-divinyl-1H-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.

ChemistryWittig reactionGeneral MedicineCombinatorial chemistryAcceptorChemInform
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Synthetically attractive indolization processes and newer methods for the preparation of selectively substituted indoles

1988

The synthetically interesting processes available for indolization reactions are discussed and illustrated in tabular form and particular emphasis is placed on the more recent methods.

Bicyclic moleculeChemistryOrganic ChemistryOrganic chemistryJournal of Heterocyclic Chemistry
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