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The Catalytic Amination of Alcohols

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TLDR
In this article, the synthesis of amines by the amination of alcohols, by means of the so-called borrowing hydrogen methodology, is presented Compared to other synthetic methodologies for the synthesis, these transformations are highly attractive because often alcohols are readily available starting materials, some of them on a large scale from renewable sources.
Abstract
In this Minireview, the synthesis of amines by the amination of alcohols, by means of the so-called borrowing hydrogen methodology, is presented Compared to other synthetic methodologies for the synthesis of amines, these transformations are highly attractive because often alcohols are readily available starting materials, some of them on a large scale from renewable sources In addition, the amination of alcohols produces water as the only by-product, which makes the process potentially environmentally benign Already today, lower alkyl amines are produced in bulk by the chemical industry with this synthetic method In particular, the recent progress applying organometallic catalysts based on iridium, ruthenium, and other metals will be discussed Notable recent achievements include the conversion of challenging substrates such as diols, the development of recyclable catalysts, milder reaction temperatures, and the direct alkylation of ammonia or its equivalents with alcohols

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Citations
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Applications of acceptorless dehydrogenation and related transformations in chemical synthesis.

TL;DR: Acceptorless dehydrogenation and related dehydrogenative coupling reactions have the potential for redirecting synthetic strategies to the use of sustainable resources, devoid of toxic reagents and deleterious side reactions, with no waste generation.
Journal ArticleDOI

Bond Activation and Catalysis by Ruthenium Pincer Complexes

TL;DR: The heterolytic activation of dihydrogen by NH/H2 MLC was reported by Fryzuk and co-workers in 1987 with pincer Ir and Rh complexes, and complex 73 was found to be an active dehydrogenation catalyst for ammoniaborane and hydrogenation reactions as discussed below.
Journal ArticleDOI

Advances in One-Pot Synthesis through Borrowing Hydrogen Catalysis

TL;DR: The objective of the present review is to give a global overview on the topic starting from those contributions published prior to the emergence of the BH concept to the most recent and current research under the term of BH catalysis.
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Substitution of alcohols by N-nucleophiles via transition metal-catalyzed dehydrogenation

TL;DR: This critical review summarizes the recent advances in "BH" substitution of alcohols by N-nucleophiles since 2009 and provides new principles for establishing green processes to replace the relevant traditional synthetic methods for C-N bond formation.
References
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Journal ArticleDOI

Atom Economy—A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way

TL;DR: The ability of transition metal complexes to preorganize π-electron systems serves as the basis both of simple additions usually accompanied by subsequent hydrogen shifts and of cycloadditions as mentioned in this paper.
Journal ArticleDOI

Hydroamination: direct addition of amines to alkenes and alkynes.

TL;DR: Hydroamination of Alkenes and Alkynes under Microwave Irradiation and Nitromercuration Reactions 3878 9.8.4.5.
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