Regio- and Enantioselective\nNickel-Catalyzed Ipso-\nand Remote Hydroamination Utilizing Organic Azides as Amino Sources\nfor the Synthesis of Primary Amines

Primary amines serve as key synthetic precursors to most\nother <i>N</i>-containing compounds, which are important\nin organic \nand medicinal chemistry. Herein, we present a NiH-catalyzed mild ipso-\nand remote hydroamination technique that utilizes organic azides as\ndeprotectable primary amine sources. This strategy offers a highly\nflexible platform for the efficient construction of α-chiral\nbranched primary amines, as well as linear primary amines.

Publication Details

Journal
Figshare
Published
2024-10-23
DOI
https://doi.org/10.1021/jacs.4c12324.s001
Primary Topic
Genetic diversity and population structure
Type
article
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article

Regio- and Enantioselective\nNickel-Catalyzed Ipso-\nand Remote Hydroamination Utilizing Organic Azides as Amino Sources\nfor the Synthesis of Primary Amines

Figshare
Genetic diversity and population structure
article

Regio- and Enantioselective\nNickel-Catalyzed Ipso-\nand Remote Hydroamination Utilizing Organic Azides as Amino Sources\nfor the Synthesis of Primary Amines

article en

Abstract

Primary amines serve as key synthetic precursors to most\nother <i>N</i>-containing compounds, which are important\nin organic \nand medicinal chemistry. Herein, we present a NiH-catalyzed mild ipso-\nand remote hydroamination technique that utilizes organic azides as\ndeprotectable primary amine sources. This strategy offers a highly\nflexible platform for the efficient construction of α-chiral\nbranched primary amines, as well as linear primary amines.

Figshare
Openalex Percentile: Top 49%
Genetic diversity and population structure
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Regio- and Enantioselective\nNickel-Catalyzed Ipso-\nand Remote Hydroamination Utilizing Organic Azides as Amino Sources\nfor the Synthesis of Primary Amines · Figshare (2024) | TGRS Research Map | TGRS