Dirhodium (II)-Catalyzed Synthesis of N-(Arylsulfonyl) hydrazines by N–H Amination of Aliphatic Amines

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Dirhodium (II)-Catalyzed Synthesis of N-(Arylsulfonyl) hydrazines by N–H Amination of Aliphatic Amines ; volume:33 ; number:04 ; year:2022 ; pages:367-370
Synlett ; 33, Heft 04 (2022), 367-370

Contributor: Ito, Motoki
Hasegawa, Yui
Saito, Satomi
Onda, Asami
Higuchi, Kazuhiro
Sugiyama, Shigeo

DOI: 10.1055/s-0041-1737759

URN: urn:nbn:de:101:1-2022040510170331776050

Rights: Kein Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:34 AM CEST

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Ito, Motoki
Hasegawa, Yui
Saito, Satomi
Onda, Asami
Higuchi, Kazuhiro
Sugiyama, Shigeo

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Asymmetric synthesis of γ-branched amines via rhodium-catalyzed reductive amination

Ruthenium-Catalyzed Enantioselective Reductive Amination

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Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines

Co‐Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions

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Co Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions

Iridium-Catalyzed Regio- and Enantioselective Amination

Iron-Catalyzed Amination of Aromatic Bromides

Aliphatic Amines Formed by Asymmetric Copper-Catalyzed Hydroamination

Cu‐Catalyzed Coupling of Aliphatic Amines with Alkylboronic Esters

Palladium‐Catalyzed Hydroaminocarbonylation of Olefins with Aliphatic Amines without Additives

Asymmetric synthesis of γ-branched amines via rhodium-catalyzed reductive amination

Ruthenium-Catalyzed Enantioselective Reductive Amination

Iridium-catalyzed direct asymmetric reductive amination utilizing primary alkyl amines as the N-sources

Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines

Co‐Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions

Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines

Co Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions

Iridium-Catalyzed Regio- and Enantioselective Amination

Iron-Catalyzed Amination of Aromatic Bromides

Aliphatic Amines Formed by Asymmetric Copper-Catalyzed Hydroamination

Cu‐Catalyzed Coupling of Aliphatic Amines with Alkylboronic Esters

Palladium‐Catalyzed Hydroaminocarbonylation of Olefins with Aliphatic Amines without Additives

Asymmetric synthesis of γ-branched amines via rhodium-catalyzed reductive amination

Ruthenium-Catalyzed Enantioselective Reductive Amination

Iridium-catalyzed direct asymmetric reductive amination utilizing primary alkyl amines as the N-sources

Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines

Co‐Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions

Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines

Co Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions

Iridium-Catalyzed Regio- and Enantioselective Amination

Iron-Catalyzed Amination of Aromatic Bromides

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Dirhodium (II)-Catalyzed Synthesis of N-(Arylsulfonyl) hydrazines by N–H Amination of Aliphatic Amines

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Other Objects (12)

Aliphatic Amines Formed by Asymmetric Copper-Catalyzed Hydroamination

Cu‐Catalyzed Coupling of Aliphatic Amines with Alkylboronic Esters

Palladium‐Catalyzed Hydroaminocarbonylation of Olefins with Aliphatic Amines without Additives

Asymmetric synthesis of γ-branched amines via rhodium-catalyzed reductive amination

Ruthenium-Catalyzed Enantioselective Reductive Amination

Iridium-catalyzed direct asymmetric reductive amination utilizing primary alkyl amines as the N-sources

Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines

Co‐Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions

Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines

Co Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions

Iridium-Catalyzed Regio- and Enantioselective Amination

Iron-Catalyzed Amination of Aromatic Bromides

Aliphatic Amines Formed by Asymmetric Copper-Catalyzed Hydroamination

Cu‐Catalyzed Coupling of Aliphatic Amines with Alkylboronic Esters

Palladium‐Catalyzed Hydroaminocarbonylation of Olefins with Aliphatic Amines without Additives

Asymmetric synthesis of γ-branched amines via rhodium-catalyzed reductive amination

Ruthenium-Catalyzed Enantioselective Reductive Amination

Iridium-catalyzed direct asymmetric reductive amination utilizing primary alkyl amines as the N-sources

Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines

Co‐Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions

Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines

Co Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions

Iridium-Catalyzed Regio- and Enantioselective Amination

Iron-Catalyzed Amination of Aromatic Bromides

Aliphatic Amines Formed by Asymmetric Copper-Catalyzed Hydroamination

Cu‐Catalyzed Coupling of Aliphatic Amines with Alkylboronic Esters

Palladium‐Catalyzed Hydroaminocarbonylation of Olefins with Aliphatic Amines without Additives

Asymmetric synthesis of γ-branched amines via rhodium-catalyzed reductive amination

Ruthenium-Catalyzed Enantioselective Reductive Amination

Iridium-catalyzed direct asymmetric reductive amination utilizing primary alkyl amines as the N-sources

Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines

Co‐Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions

Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines

Co Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions

Iridium-Catalyzed Regio- and Enantioselective Amination

Iron-Catalyzed Amination of Aromatic Bromides

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