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Kinetic Resolution of α-Tertiary Propargylic Amines through Asymmetric Remote Aminations of Anilines

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This article is published in ACS Catalysis.The article was published on 2021-07-16. It has received 17 citations till now. The article focuses on the topics: Kinetic resolution.

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Asymmetric Synthesis of Hydroquinazolines Bearing C4-Tetrasubstituted Stereocenters via Kinetic Resolution of α-Tertiary Amines.

TL;DR: A novel protocol for asymmetric synthesis of hydroquinazolines bearing C4-tetrasubstituted stereocenters has been achieved through kinetic resolution of 2-amido α-tertiary benzylamines via chiral phosphoric acid catalyzed intramolecular dehydrative cyclizations.
Journal ArticleDOI

Kinetic resolution of N-aryl β-amino alcohols via asymmetric aminations of anilines

TL;DR: In this paper, an efficient kinetic resolution of N-aryl β-amino alcohols was developed via asymmetric para-aminations of anilines with azodicarboxylates enabled by chiral phosphoric acid catalysis.
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Enantioselective Synthesis of Planar-Chiral Macrocycles through Asymmetric Electrophilic Aromatic Amination.

TL;DR: Preliminary utilization of the planar-chiral macrocycle as chiral organocatalyst showcased the potential applications of these novel chiral skeletons.
Journal ArticleDOI

Catalytic Kinetic Resolution and Desymmetrization of Amines

TL;DR: This review systematically summarized the development of kinetic resolution and desymmetrization of amines through nonenzymatic asymmetric catalytic approaches in the last two decades.
References
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Journal ArticleDOI

Efficiency in nonenzymatic kinetic resolution.

TL;DR: The story of kinetic resolution from the early discoveries through fascinating historical milestones and conceptual developments is followed, and a focus on modern techniques that maximize efficiency is closed.
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A walk around the A3-coupling

TL;DR: This tutorial review aims to highlight the current achievements in the field of A(3)-couplings and related transformations.
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The Enantioselective Addition of Alkyne Nucleophiles to Carbonyl Groups

TL;DR: This review highlights and compares the available methods for the direct enantioselective addition of alkynes and metal alkynylide nucleophiles into prochiral aldehydes, ketones, and imines.
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Direct addition of alkynes to imines and related C=N electrophiles: A convenient access to propargylamines.

TL;DR: An overview of the most significant advances in the preparation of propargylic amines via the direct addition of alkynes to imines and related carbon-nitrogen electrophiles in the presence of metal catalysts or promoters is provided.
Journal ArticleDOI

Synthesis and Reactivity of Propargylamines in Organic Chemistry

TL;DR: The different synthetic approaches to synthesize propargylamines, such as A3 couplings and C-H functionalization of alkynes, have been described and organized on the basis of the catalysts employed in the syntheses.
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