Organocatalytic asymmetric allylic amination of Morita–Baylis–Hillman carbonates of isatins

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Bibliographic citation: Organocatalytic asymmetric allylic amination of Morita–Baylis–Hillman carbonates of isatins ; volume:8 ; pages:1241-1245
Beilstein journal of organic chemistry ; 8, 1241-1245

Classification: Chemie

DOI: 10.3762/bjoc.8.139

URN: urn:nbn:de:101:1-2012101719355

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:37 AM CEST

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Aza-Morita–Baylis–Hillman Synthesis of Benzoxazepines

Benzonaphthyridines from Morita-Baylis-Hillman Adduct Acetates

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Iron-Catalyzed Intramolecular Allylic C−H Amination

Regio- and Enantioselective Cobalt-Catalyzed Allylic Amination

Application of 7-azaisatins in enantioselective Morita–Baylis–Hillman reaction

The Morita–Baylis–Hillman Reaction

Asymmetric allylic alkylation of Morita–Baylis–Hillman carbonates with α-fluoro-β-keto esters

Aza-Morita–Baylis–Hillman Synthesis of Benzoxazepines

Benzonaphthyridines from Morita-Baylis-Hillman Adduct Acetates

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Organocatalyzed Morita-Baylis-Hillman reaction : mechanism and catalysis

Palladium-Catalyzed Enantioselective Aza-Morita–Baylis–Hillman Reaction

Engineered Biocatalyst Permits Enantioselective Morita–Baylis–Hillman Reaction

Ir-Catalyzed Allylic Amination and Etherification

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Iron-Catalyzed Intramolecular Allylic C−H Amination

Regio- and Enantioselective Cobalt-Catalyzed Allylic Amination

Application of 7-azaisatins in enantioselective Morita–Baylis–Hillman reaction

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Organocatalytic asymmetric allylic amination of Morita–Baylis–Hillman carbonates of isatins

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Other Objects (12)

The Morita–Baylis–Hillman Reaction

Asymmetric allylic alkylation of Morita–Baylis–Hillman carbonates with α-fluoro-β-keto esters

Aza-Morita–Baylis–Hillman Synthesis of Benzoxazepines

Benzonaphthyridines from Morita-Baylis-Hillman Adduct Acetates

Organocatalyzed Morita-Baylis-Hillman reaction : mechanism and catalysis

Palladium-Catalyzed Enantioselective Aza-Morita–Baylis–Hillman Reaction

Engineered Biocatalyst Permits Enantioselective Morita–Baylis–Hillman Reaction

Ir-Catalyzed Allylic Amination and Etherification

Morita–Baylis–Hillman reaction of acrylamide with isatin derivatives

Iron-Catalyzed Intramolecular Allylic C−H Amination

Regio- and Enantioselective Cobalt-Catalyzed Allylic Amination

Application of 7-azaisatins in enantioselective Morita–Baylis–Hillman reaction

The Morita–Baylis–Hillman Reaction

Asymmetric allylic alkylation of Morita–Baylis–Hillman carbonates with α-fluoro-β-keto esters

Aza-Morita–Baylis–Hillman Synthesis of Benzoxazepines

Benzonaphthyridines from Morita-Baylis-Hillman Adduct Acetates

Organocatalyzed Morita-Baylis-Hillman reaction : mechanism and catalysis

Palladium-Catalyzed Enantioselective Aza-Morita–Baylis–Hillman Reaction

Engineered Biocatalyst Permits Enantioselective Morita–Baylis–Hillman Reaction

Ir-Catalyzed Allylic Amination and Etherification

Morita–Baylis–Hillman reaction of acrylamide with isatin derivatives

Iron-Catalyzed Intramolecular Allylic C−H Amination

Regio- and Enantioselective Cobalt-Catalyzed Allylic Amination

Application of 7-azaisatins in enantioselective Morita–Baylis–Hillman reaction

The Morita–Baylis–Hillman Reaction

Asymmetric allylic alkylation of Morita–Baylis–Hillman carbonates with α-fluoro-β-keto esters

Aza-Morita–Baylis–Hillman Synthesis of Benzoxazepines

Benzonaphthyridines from Morita-Baylis-Hillman Adduct Acetates

Organocatalyzed Morita-Baylis-Hillman reaction : mechanism and catalysis

Palladium-Catalyzed Enantioselective Aza-Morita–Baylis–Hillman Reaction

Engineered Biocatalyst Permits Enantioselective Morita–Baylis–Hillman Reaction

Ir-Catalyzed Allylic Amination and Etherification

Morita–Baylis–Hillman reaction of acrylamide with isatin derivatives

Iron-Catalyzed Intramolecular Allylic C−H Amination

Regio- and Enantioselective Cobalt-Catalyzed Allylic Amination

Application of 7-azaisatins in enantioselective Morita–Baylis–Hillman reaction

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