Catalytic Reductive Amination of Aldehydes and Ketones With Nitro Compounds: New Light on an Old Reaction

Reductive amination of carbonyl compounds with primary amines is a well-established synthetic methodology for the selective production of unsymmetrically substituted secondary and tertiary amines. From the industrial and green chemistry perspective, it is attractive to combine reductive amination wi...

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Main Author: Alexey Yu. Sukhorukov
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-04-01
Series:Frontiers in Chemistry
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fchem.2020.00215/full
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spelling doaj-026f8d3a989044ccacf92db07eb2cde32020-11-25T02:53:50ZengFrontiers Media S.A.Frontiers in Chemistry2296-26462020-04-01810.3389/fchem.2020.00215528982Catalytic Reductive Amination of Aldehydes and Ketones With Nitro Compounds: New Light on an Old ReactionAlexey Yu. Sukhorukov0Alexey Yu. Sukhorukov1Laboratory of Organic and Metal-organic Nitrogen-Oxygen Systems, N. D. Zelinsky Institute of Organic Chemistry, Moscow, RussiaDepartment of Innovational Materials and Technologies Chemistry, Plekhanov Russian University of Economics, Moscow, RussiaReductive amination of carbonyl compounds with primary amines is a well-established synthetic methodology for the selective production of unsymmetrically substituted secondary and tertiary amines. From the industrial and green chemistry perspective, it is attractive to combine reductive amination with the synthesis of primary amines in a single one-pot catalytic process. In this regard, nitro compounds, which are readily available and inexpensive feedstocks, received much attention as convenient precursors to primary amines in such processes. Although the direct reductive coupling of nitro compounds with aldehydes/ketones to give secondary and tertiary amines has been known since the 1940's, due to the development of highly efficient and selective non-noble metal-based catalysts a breakthrough in this area was made in the last decade. In this short overview, recent progress in the methodology of the reductive amination with nitro compounds is summarized together with applications to the synthesis of bioactive amines and heterocycles. Remaining challenges in this field are also analyzed.https://www.frontiersin.org/article/10.3389/fchem.2020.00215/fullnitro compoundsreductive aminationsecondary aminesheterogeneous catalysiscyclizationsnitrogen heterocycles
collection DOAJ
language English
format Article
sources DOAJ
author Alexey Yu. Sukhorukov
Alexey Yu. Sukhorukov
spellingShingle Alexey Yu. Sukhorukov
Alexey Yu. Sukhorukov
Catalytic Reductive Amination of Aldehydes and Ketones With Nitro Compounds: New Light on an Old Reaction
Frontiers in Chemistry
nitro compounds
reductive amination
secondary amines
heterogeneous catalysis
cyclizations
nitrogen heterocycles
author_facet Alexey Yu. Sukhorukov
Alexey Yu. Sukhorukov
author_sort Alexey Yu. Sukhorukov
title Catalytic Reductive Amination of Aldehydes and Ketones With Nitro Compounds: New Light on an Old Reaction
title_short Catalytic Reductive Amination of Aldehydes and Ketones With Nitro Compounds: New Light on an Old Reaction
title_full Catalytic Reductive Amination of Aldehydes and Ketones With Nitro Compounds: New Light on an Old Reaction
title_fullStr Catalytic Reductive Amination of Aldehydes and Ketones With Nitro Compounds: New Light on an Old Reaction
title_full_unstemmed Catalytic Reductive Amination of Aldehydes and Ketones With Nitro Compounds: New Light on an Old Reaction
title_sort catalytic reductive amination of aldehydes and ketones with nitro compounds: new light on an old reaction
publisher Frontiers Media S.A.
series Frontiers in Chemistry
issn 2296-2646
publishDate 2020-04-01
description Reductive amination of carbonyl compounds with primary amines is a well-established synthetic methodology for the selective production of unsymmetrically substituted secondary and tertiary amines. From the industrial and green chemistry perspective, it is attractive to combine reductive amination with the synthesis of primary amines in a single one-pot catalytic process. In this regard, nitro compounds, which are readily available and inexpensive feedstocks, received much attention as convenient precursors to primary amines in such processes. Although the direct reductive coupling of nitro compounds with aldehydes/ketones to give secondary and tertiary amines has been known since the 1940's, due to the development of highly efficient and selective non-noble metal-based catalysts a breakthrough in this area was made in the last decade. In this short overview, recent progress in the methodology of the reductive amination with nitro compounds is summarized together with applications to the synthesis of bioactive amines and heterocycles. Remaining challenges in this field are also analyzed.
topic nitro compounds
reductive amination
secondary amines
heterogeneous catalysis
cyclizations
nitrogen heterocycles
url https://www.frontiersin.org/article/10.3389/fchem.2020.00215/full
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