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Amide reduction

Amide reduction is a key transformation in organic synthesis wherein the carbonyl group of an amide is cleaved and reduced to yield either amines or aldehydes, enabling the construction of these vital functional groups from abundant amide starting materials.^[1]^[2] The traditional approach utilizes strong hydride donors such as lithium aluminum hydride (LiAlH₄) in ether solvents, which reduces primary, secondary, and tertiary amides to the corresponding primary, secondary, and tertiary amines through initial nucleophilic addition of hydride to the carbonyl, formation of an iminium ion intermediate, and final reduction, often achieving high yields like 95% for N-methyldodecanamide to N-methyldodecylamine.^[1]^[3] Selective reduction of tertiary amides to aldehydes, rather than over-reduction to amines, can be accomplished with milder reagents like disiamylborane (Sia₂BH) or Schwartz's reagent (Cp₂Zr(H)Cl), which proceed via hydroboration or hydrozirconation mechanisms that halt at the aldehydic stage after hydrolysis, offering utility in sensitive substrates.^[3]^[4] Contemporary methods emphasize catalysis for enhanced chemoselectivity and sustainability, including nickel- or zinc-catalyzed hydrosilylation with silanes under mild conditions that tolerate esters and nitro groups, as well as ruthenium pincer complex-mediated hydrogenation with molecular H₂ at moderate pressures (30–50 bar) and temperatures (up to 160°C), producing amines via deoxygenation with preservation of the C–N bond while generating minimal waste.^[2]^[5]^[6] These catalytic protocols, often employing earth-abundant metals, address limitations of stoichiometric reductants like hazardous byproducts and poor functional group tolerance, thereby supporting efficient synthesis of pharmaceuticals and fine chemicals in line with green chemistry goals.^[7]^[5]

Fundamentals

Definition and Scope

Amide reduction encompasses the chemical transformation of the carbonyl group in amides, characterized by the general structure R-C(O)-NR_2, into either a methylene (CH_2) unit yielding amines (R-CH_2-NR_2) or a formyl (CHO) group producing aldehydes (R-CHO). This reaction serves as a cornerstone in organic synthesis, enabling the conversion of stable amide precursors into valuable amine or aldehyde derivatives. The process applies broadly to primary (NR_2 = NH_2), secondary (NR_2 = NHR'), and tertiary (NR_2 = NR'R'') amides, with selectivity determining the product outcome—full reduction typically affords amines, while partial reduction targets aldehydes.^[2]^[8] The inherent stability of amides stems from resonance delocalization of the nitrogen lone pair into the carbonyl π-system, which imparts partial double-bond character to the C-N bond and diminishes the electrophilicity of the carbonyl carbon relative to other carbonyl compounds such as aldehydes, ketones, or esters. This resonance stabilization necessitates the use of potent reducing agents to overcome the kinetic and thermodynamic barriers, distinguishing amide reduction from more facile reductions of less stabilized carbonyls.^[9] Historically, the reduction of amides using metal hydrides was first documented in the late 1940s, marking the advent of reliable methods for this transformation shortly after the discovery of lithium aluminum hydride in 1947.^[10] Amide reduction holds significant importance in the synthesis of pharmaceuticals, agrochemicals, and natural products, where it facilitates the late-stage installation of amine or aldehyde moieties essential for biological activity and structural diversity.^[11]

Types of Products

Amide reduction reactions can produce distinct classes of products depending on the degree of reduction and the substitution pattern of the amide. Full reduction of primary amides (RCONH₂) proceeds to primary amines (RCH₂NH₂), involving the cleavage of the C=O bond and addition of four equivalents of hydrogen, as represented by the general equation:

\text{RCONH}_2 + 4[\text{H}] \rightarrow \text{RCH}_2\text{NH}_2 + \text{H}_2\text{O}

This transformation effectively reduces the carbonyl to a methylene group. Full reduction of secondary amides (RCONHR') proceeds to secondary amines (RCH₂NHR'), involving the cleavage of the C=O bond and addition of four equivalents of hydrogen, as represented by the general equation:

\text{RCONHR'} + 4[\text{H}] \rightarrow \text{RCH}_2\text{NHR'} + \text{H}_2\text{O}

This transformation effectively reduces the carbonyl to a methylene group while retaining the nitrogen substituent. Full reduction of tertiary amides (RCONR'R'') proceeds to tertiary amines (RCH₂NR'R''), following a similar pattern.^[12]^[3] In contrast, partial reduction of primary amides (RCONH₂) can generate aldehydes (RCHO) and ammonia (NH₃), requiring only two equivalents of hydrogen and halting at the aldehydic stage:

\text{RC(O)NH}_2 + 2[\text{H}] \rightarrow \text{RCHO} + \text{NH}_3

Partial reduction targets N,N-disubstituted (tertiary) amides (RC(O)NR₂) to generate aldehydes (RCHO) and the corresponding amine (HNR₂), requiring only two equivalents of hydrogen and halting at the aldehydic stage after hydrolysis:

\text{RC(O)NR}_2 + 2[\text{H}] \rightarrow \text{RCHO} + \text{HNR}_2

This selective process exploits the amide's resonance stabilization to limit over-reduction.^[12] Achieving selectivity between amine and aldehyde products hinges on factors such as steric hindrance around the amide carbonyl, the nature of the reducing agent, and reaction conditions like temperature and solvent, which collectively mitigate risks of over-reduction to hydrocarbons or formation of byproducts.^[12] Rare special cases include complete deoxygenation to hydrocarbons (e.g., RCH₃ from RCONHR), typically requiring specialized hydride systems beyond standard protocols. Key challenges in these reductions encompass preventing side products like alcohols from competing pathways and ensuring high yield in aldehyde-directed syntheses by avoiding further reduction to primary alcohols.^[12]

Reduction to Amines

Catalytic Hydrogenation

Catalytic hydrogenation represents a classical method for the complete reduction of amides to amines, leveraging molecular hydrogen and heterogeneous catalysts to overcome the inherent stability of the amide bond due to resonance delocalization between the carbonyl and nitrogen lone pair.^[13] This process typically proceeds via a stepwise mechanism involving initial activation of the carbonyl group on the catalyst surface, followed by sequential addition of hydrogen to form intermediates such as hemiaminals or iminols, and ultimately cleavage of the C-N bond to yield the amine product and water.^[13] The overall transformation can be represented by the general equation:

\mathrm{RC(O)NR'_2 + 2H_2 \rightarrow RCH_2NR'_2 + H_2O}

where \mathrm{R} and \mathrm{R'} denote alkyl or aryl substituents.^[14] The reaction requires elevated temperatures and pressures to achieve practical rates, with typical conditions ranging from 150–250°C and 100–300 atm of hydrogen pressure.^[14] Common catalysts include copper-chromium oxide (CuCr₂O₄, often promoted with barium or manganese oxides), Raney nickel, and rhenium heptoxide (Re₂O₇), which facilitate hydrogen activation and substrate adsorption. For instance, copper-chromium oxide catalysts, pioneered by Homer Adkins in the 1930s, effectively reduce primary, secondary, and tertiary amides under these harsh conditions, though selectivity can vary with the amide substitution pattern.^[14] Raney nickel operates similarly at around 250°C, offering good activity for aliphatic amides but requiring careful handling due to its pyrophoric nature. A representative example is the reduction of acetanilide (CH₃CONHC₆H₅) to N-ethylaniline (CH₃CH₂NHC₆H₅), achieved using copper-chromium oxide catalyst at 200–225°C and 200–300 atm, yielding the product in high conversion after several hours.^[14] This method has found industrial application in the synthesis of amine precursors for nylon polymers, particularly through the hydrogenation of fatty acid amides to aliphatic amines used in polyamide production.^[5] The primary advantages of catalytic hydrogenation lie in its scalability for large-scale manufacturing, as it employs inexpensive hydrogen gas and avoids stoichiometric reductants, producing only water as a byproduct.^[13] However, the need for high-pressure equipment and elevated temperatures limits its use in fine chemical synthesis, while catalysts like copper-chromium oxide pose environmental concerns due to chromium toxicity, necessitating careful disposal and recovery protocols.^[5] Developed primarily in the 1930s and 1940s by researchers such as Adkins for the reduction of fatty acid amides, this approach laid the foundation for subsequent milder catalytic innovations.^[14]

Hydride Reduction Methods

Hydride reduction methods employ stoichiometric metal hydrides to convert amides into amines by delivering hydride ions to the carbonyl group, resulting in complete deoxygenation and reduction of the C-N bond to a methylene group. Lithium aluminum hydride (LiAlH₄) is the archetypal reagent for this transformation, applicable to primary, secondary, and tertiary amides, yielding the corresponding amines in good to excellent yields under refluxing conditions in ether or tetrahydrofuran solvents.^[15] The general reaction can be represented as:

\text{RC(O)NR}_2 + 4[\text{H}] \xrightarrow{\text{LiAlH}_4} \text{RCH}_2\text{NR}_2 + \text{H}_2\text{O}

This method, first demonstrated in the late 1940s, provides a straightforward route for laboratory-scale synthesis but requires careful handling due to the reagent's reactivity.^[15] The mechanism begins with nucleophilic attack by hydride on the amide carbonyl, forming a tetrahedral intermediate, followed by elimination of the amine leaving group to generate an iminium ion intermediate. Subsequent hydride additions reduce the iminium to the final amine product. Primary amides exhibit high selectivity, often proceeding without significant side reactions, as exemplified by the reduction of benzamide to benzylamine in diethyl ether, affording the product in approximately 80% yield after acidic workup.^[16]^[15] Variations include borane complexes such as BH₃·THF, which offer faster reaction rates, particularly for tertiary amides, due to the reagent's milder conditions and compatibility with certain functional groups like olefins. Borane reductions proceed via coordination to the carbonyl oxygen, enhancing electrophilicity and facilitating hydride transfer, often completing in hours at room temperature. For milder conditions, sodium borohydride (NaBH₄) combined with additives like iodine or titanium(IV) chloride enables selective reduction of secondary and tertiary amides to amines, avoiding the harshness of LiAlH₄ while achieving yields up to 76% in tetrahydrofuran.^[17] Diisobutylaluminum hydride (DIBAL-H) is occasionally used for amine formation with excess reagent but is primarily noted for partial reduction to aldehydes (see Reduction to Aldehydes section). Limitations of these hydride methods include risks of over-reduction for substrates with sensitive groups like nitro or cyano functionalities, as well as the necessity for rigorous aqueous workup to hydrolyze aluminum or boron salts, which can complicate purification.^[3]

Alternative Catalytic Approaches

One prominent class of alternative catalytic approaches involves the use of silanes as hydride donors in the presence of earth-abundant metal catalysts, such as iron or nickel, to achieve deoxygenative reduction of amides to amines under mild conditions. In a seminal 2009 report, Beller and coworkers demonstrated the first general iron-catalyzed hydrosilylation of secondary and tertiary amides using polymethylhydrosiloxane (PMHS) as the reducing agent and Fe₃(CO)₁₂ as the precatalyst, proceeding at 65–100 °C in toluene to afford amines in yields up to 99% for a range of substrates including aliphatic and aromatic amides.^[18] The reaction leverages the activation of the silane by low-valent iron species, facilitating C=O bond cleavage and hydride transfer, with byproducts forming siloxanes that can be easily separated. Similarly, in 2017, Garg and colleagues developed a nickel-catalyzed protocol employing NiCl₂(dme) with phenylsilane (PhSiH₃) at 115 °C, enabling selective reduction of secondary and tertiary amides, including lactams, to amines in yields exceeding 90% while tolerating esters and preserving stereocenters. These silane-mediated methods offer advantages over traditional hydrogenation by operating at lower pressures and temperatures, avoiding the need for high-pressure hydrogen gas, and utilizing inexpensive, non-toxic reducing agents.^[19] A distinct two-step catalytic route involves initial thionation of amides to thioamides using Lawesson's reagent, followed by desulfurization with Raney nickel to yield amines under ambient conditions. This method, detailed in a 2021 review by Yousuf et al., proceeds via reflux in toluene for thionation (yields >80% for diverse amides) and subsequent room-temperature treatment with Raney Ni in ethanol or acetone, affording amines without harsh reductants.^[20] The process benefits from the mildness of Raney Ni, which selectively removes sulfur while preserving sensitive functionalities, making it suitable for complex molecule synthesis. In the 2020s, cobalt-based catalysis gained traction for hydroamination-like reductions of amides. Beller and coworkers reported a homogeneous Co(NTf₂)₂/(p-anisyl)triphos system with [Me₃SiOTf] cocatalyst, enabling deoxygenative hydrogenation at 100 °C and 30 bar H₂ to produce amines from secondary and tertiary amides in yields up to 95%, with broad substrate scope including cyclic lactams.^[21] This method underscores cobalt's efficacy in promoting C-O cleavage via hemiaminal intermediates, offering scalability and tolerance to functional groups like halides and alkenes. Overall, these alternatives provide versatile, operationally simple pathways that expand beyond conventional hydrogenation, emphasizing sustainability through base metals and mild reagents.

Reduction to Aldehydes

Noncatalytic Methods

One of the cornerstone noncatalytic approaches to partial amide reduction involves the use of diisobutylaluminum hydride (DIBAL-H) as a stoichiometric reagent, particularly effective for converting tertiary amides to aldehydes under low-temperature conditions, typically at -78°C in solvents like toluene or dichloromethane.^[22] The reaction proceeds via a single hydride transfer, represented by the equation:

\ce{RC(O)NR'_2 + DIBAL-H -> RCHO + (iBu)_2AlNR'_2}

This selectivity arises because the aluminum coordinates to both the emerging aldehyde oxygen and the nitrogen lone pair, forming a stable five-membered chelate that inhibits further hydride addition or over-reduction to the alcohol.^[23] The method is broadly applicable to aliphatic, aromatic, and heteroaromatic tertiary amides, often delivering yields exceeding 80% when 1-1.2 equivalents of DIBAL-H are employed.^[22] A specialized application leverages Weinreb amides (N-methoxy-N-methylamides), which undergo clean reduction to aldehydes with DIBAL-H, even at temperatures up to -40°C, owing to enhanced chelation involving the methoxy oxygen that stabilizes the intermediate and blocks excess reagent reactivity.^[24] This variant has found utility in complex syntheses. The Sonn-Müller method represents an earlier stoichiometric route, primarily for N-aryl amides, entailing activation with phosphorus pentachloride (PCl5) to generate an imidoyl chloride intermediate, followed by reduction with tin(II) chloride in concentrated hydrochloric acid to form an iminium salt, and mild hydrolysis to the aldehyde.^[25] Though less prevalent in modern practice due to its harsh conditions and lower functional group tolerance, it remains relevant for specific aromatic systems where hydride methods falter.^[25] Under carefully controlled conditions, such as modified formulations or specific solvent systems, lithium aluminum hydride (LiAlH₄) can partially reduce N,N-dialkylamides to aldehydes, for example, via 1-acylaziridine intermediates with LiAlH₄, or other variants like lithium tri-tert-butoxyaluminum hydride, to enhance selectivity and prevent progression to amines.^[26] These adaptations deliver moderate to good yields for dialkyl substrates but demand precise stoichiometry to minimize over-reduction.^[26] Despite their efficacy, these noncatalytic methods share limitations, including high sensitivity to over-reduction if temperatures exceed -78°C or excess reagent is used, as the chelate can dissociate, allowing secondary hydride additions leading to alcohols in up to 20-30% yields under suboptimal conditions.^[27] All require rigorously anhydrous environments, as the organoaluminum or metal hydrides react violently with moisture, complicating handling and necessitating inert atmospheres.^[24]

Catalytic Methods

Catalytic methods for the reduction of amides to aldehydes primarily rely on hydrosilylation strategies, which employ transition metal catalysts to facilitate the addition of silanes to the amide carbonyl, yielding silyl-protected intermediates that hydrolyze to aldehydes. These approaches offer enhanced selectivity compared to traditional stoichiometric reductions, minimizing over-reduction to amines or alcohols. One seminal method involves hydrozirconation using Schwartz's reagent, Cp₂ZrHCl, which reacts with tertiary amides at room temperature to form a zirconacycle intermediate, followed by hydrolysis to the aldehyde. This process achieves high yields (up to 95%) for aromatic and aliphatic tertiary amides, including Weinreb amides, while tolerating esters and other functional groups. Although typically stoichiometric in the zirconium reagent, its mild conditions (0–25°C, toluene solvent, 1–2 hours) and chemoselectivity have inspired catalytic variants. The mechanism proceeds via η²-coordination of the amide to zirconium, followed by hydride migration and elimination of the amine. Titanium-catalyzed hydrosilylation represents a truly catalytic advancement, particularly from developments in the 2010s. Using Ti(OiPr)₄ (5–10 mol%) with 1,1,3,3-tetramethyldisiloxane (TMDS) as the hydrosilane, secondary and tertiary amides are reduced to aldehydes in good yields (70–90%) under mild conditions (room temperature, 24 hours, methylcyclohexane solvent). For example, N,N-diethylbenzamide yields benzaldehyde selectively without over-reduction. This system extends to primary aromatic amides, though with moderate efficiency, and avoids the toxicity of diphenylsilane by employing the cheaper TMDS. The reaction likely involves formation of a titanium-silyl species that adds across the C=O bond, generating a silyl hemiaminal that eliminates to the aldehyde upon workup. Ruthenium-catalyzed hydrosilylation provides an alternative organometallic route, often via activation of the amide to an iminoyl chloride intermediate. Treatment of secondary amides with oxalyl chloride generates the iminoyl chloride, which undergoes selective hydrosilylation with PhMe₂SiH using a ruthenium catalyst (e.g., RuH₂(PPh₃)₄, 1–5 mol%) at 50°C, yielding the aldehyde after hydrolysis (yields 60–85%). This two-step process adapts principles from classical reductions like the Rosenmund reaction for acid chlorides, achieving selectivity for aldehyde formation from aliphatic and aromatic substrates while handling sensitive groups. Conditions remain mild (0–50°C overall), but require careful handling of the activation step.^[28] These catalytic hydrosilylation methods excel in avoiding over-reduction to amines, a common issue in noncatalytic approaches, due to the controlled delivery of hydride equivalents and stabilization of intermediates. However, challenges include the relatively high cost of transition metal catalysts and the need to manage siloxane byproducts from silane consumption. Ongoing refinements focus on earth-abundant metals to improve scalability.^[28] The general equation for hydrosilylation-based reduction is:

\mathrm{RC(O)NR'_2 + HSiR''_3 \xrightarrow{\text{catalyst}} RCH(OSiR''_3)NHR'_2 \xrightarrow{\mathrm{H_2O}} RCHO + HNR'_2 + (R''_3Si)_2O

This pathway underscores the efficiency of catalytic systems in achieving partial reduction.

Recent Developments

Transition Metal Innovations

Recent innovations in transition metal catalysis have expanded the scope of amide reductions, particularly for challenging unactivated substrates, by leveraging copper(I) systems for site-selective hydrogenation. A bifunctional catalyst combining Cu(I) with an N-heterocyclic carbene and a guanidine organocatalyst enables the first Cu(I)-catalyzed hydrogenation of amides using molecular hydrogen, targeting difficult-to-reduce unactivated alkyl and heterocycle-derived amides with high chemoselectivity via hydrogen-bonding recognition. The reaction proceeds under mild conditions of 70°C and 100 bar H₂ in 1,4-dioxane, employing 10–20 mol% catalyst loading and 1.3–2.5 equiv NaOᵗBu as base, affording amines in good yields while tolerating sensitive functional groups.^[29] The transformation follows the general scheme for deoxygenative reduction:

\text{RC(O)NHR'} + \text{H}_2 \xrightarrow{\text{Cu(I) cat., base}} \text{RCH}_2\text{NHR'}

This approach demonstrates improved temperature control compared to classical catalytic hydrogenation, which typically demands >150°C and pressures exceeding 100 bar for unactivated amides.^[29] Nickel and cobalt catalysts have also seen post-2022 progress in reductive transformations involving amides, often integrating reduction steps into broader synthetic sequences. Nickel catalysis facilitates ester-to-amide conversion followed by reduction, as in a 2023 Ni-based reductive amidation of esters with nitroarenes under hydrogen, yielding amides that undergo subsequent Ni-promoted deoxygenation to amines with high efficiency and broad substrate tolerance.^[30] Complementing this, a 2024 cobalt carbonyl system enables light-promoted hydroaminocarbonylation of alkenes with amines at low pressure (1–5 bar CO/H₂) and room temperature, producing amides that can be directly reduced in tandem to amines using silane additives, streamlining access to complex amine scaffolds.^[31] Zirconium-based catalysis has advanced the selective reduction of tertiary amides to aldehydes through a 2023 catalytic protocol using 5 mol% Cp₂ZrCl₂ to generate zirconocene hydride intermediates. This mild, divergent semireduction converts tertiary amides to imines at room temperature in toluene, followed by acidic hydrolysis to afford aldehydes in yields up to 94%, with exceptional chemoselectivity over esters, nitriles, and other reducible groups.^[32] The method outperforms stoichiometric Schwartz's reagent (Cp₂Zr(H)Cl) by enabling turnover and avoiding over-reduction. These transition metal innovations have found application in pharmaceutical synthesis, such as preparing amine intermediates for piperazine- and morpholine-based drug candidates by site-selective Cu(I) reduction of polyfunctional amides, enhancing step economy in late-stage diversification.^[29] Overall, they reduce reliance on harsh conditions, with pressures as low as 1 bar in Co systems and temperatures below 100°C, contrasting classical methods and improving sustainability in amine and aldehyde production.^[31]

Metal-Free and Sustainable Strategies

Electrochemical methods represent a cornerstone of metal-free amide reduction, leveraging electricity as a clean reductant to generate hydride species in situ, often in protic solvents like water or alcohols for enhanced sustainability. These approaches typically involve cathodic reduction, where electrons facilitate deoxygenation of the amide carbonyl to form amines, bypassing the need for hazardous reducing agents or high-pressure hydrogen gas. A seminal example is the hydrosilane-mediated electrochemical reduction reported in 2021, which uses phenylsilane as a hydrogen donor on a carbon cathode, achieving up to 99% yield for the conversion of tertiary amides to amines under mild conditions (room temperature, undivided cell).^[33] The process proceeds via a ketyl radical intermediate, enabling selective C-O bond cleavage. The general reaction can be represented as:

\text{RC(O)NR}_2 + 2e^- + 2\text{H}^+ \rightarrow \text{RCH}_2\text{NR}_2 + \text{H}_2\text{O}

This equation illustrates the two-electron, two-proton transfer essential for deoxygenative reduction. Reviews from 2018 to 2024 underscore the versatility of such electrosyntheses for carbonyl compounds, including amides, with applications in pharmaceutical synthesis due to their atom economy and compatibility with renewable energy sources.^[34] Advantages include minimal waste generation and scalability, as demonstrated by continuous-flow setups that enhance efficiency while using earth-abundant electrodes like graphite or lead. Organocatalytic strategies further advance sustainable amide reduction by employing non-metallic Lewis acids to activate the amide for hydrosilylation with inexpensive silanes, yielding amines without toxic byproducts. Boron-based catalysts, such as tris(pentafluorophenyl)borane [B(C₆F₅)₃], have emerged as highly effective, promoting the reduction of secondary and tertiary amides under mild conditions (e.g., 60–80°C, toluene or solvent-free). A 2008 seminal study established the chemoselectivity of this approach for tertiary amides, achieving >90% yields while sparing esters and nitro groups.^[35] More recent advancements, detailed in a 2023 review, highlight extensions to primary amides using polymethylhydrosiloxane (PMHS) or tetramethyldisiloxane (TMDS) as green, air-stable reductants, with catalyst loadings as low as 5 mol% and turnover numbers exceeding 100.^[36] For instance, B(C₆F₅)₃ facilitates the activation of the amide nitrogen, enabling nucleophilic attack by silane to form silylated intermediates that hydrolyze to amines. Calcium(II) triflimide [Ca(NTf₂)₂], an earth-abundant organocatalyst, has been explored in 2023 for related hydrosilylation activations of imine intermediates, offering high functional group tolerance.^[37] These methods prioritize sustainability through recyclable catalysts and avoidance of precious metals, with E-factors often below 5, making them suitable for industrial-scale amine production. Biocatalytic reductions of amides remain an emerging frontier, adapting enzymes like imine reductases to handle amide-derived substrates in aqueous media for enantioselective amine synthesis. A 2023 report demonstrated engineered reductive aminases (RedAms) for the stereoselective reduction of cyclic imines in reductive amination processes, achieving >95% ee in buffer systems at ambient temperature and pH 7–9.^[38] This approach leverages cofactor recycling (e.g., NADPH via glucose dehydrogenase) to minimize waste, with conversions up to 80% for secondary amine products. While direct amide reduction is limited, these adaptations fill a gap in green chemistry by enabling mild, metal-free conditions compatible with bio-based feedstocks. Green chemistry principles are integrated across these strategies through the use of water or bio-derived solvents, such as ethanol. Overall, these metal-free methods offer significant advantages over conventional techniques, including reduced toxicity, lower environmental impact, and improved selectivity, addressing key sustainability challenges in amide reduction.

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Aug 17, 2023 · Here, we present a robust methodology for amide synthesis compared to traditional amidation reactions: the reductive amidation of esters with ...
[32]
Cobalt-catalyzed synthesis of amides from alkenes and amines ...
Jan 4, 2024 · We report an alkene hydroaminocarbonylation catalyzed by unmodified, inexpensive cobalt carbonyl under mild conditions and low pressure promoted by light.
[33]
Mild Divergent Semireductive Transformations of Secondary and Tertiary Amides via Zirconocene Hydride Catalysis
### Abstract and Key Points on Cp2Zr(H)Cl for Tertiary Amides to Aldehydes (2023)
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Hydrosilane-Mediated Electrochemical Reduction of Amides
Jun 21, 2021 · Electrochemical reduction of amides was achieved by using a hydrosilane without any toxic or expensive metals.Missing: photoelectrochemical | Show results with:photoelectrochemical
[35]
Electrosynthesis of amides: Achievements since 2018 and prospects
Jun 15, 2024 · Moreover, amides are vital intermediates for the synthesis of other types of molecules, including amines, isonitriles, and N-heterocycles.
[36]
Highly Chemoselective Metal-Free Reduction of Tertiary Amides
This communication describes the chemoselective metal-free reduction of tertiary amides to the corresponding amines.
[37]
Metal‐Free Catalytic Reduction of Amides: Recent Progress - 2023
Mar 27, 2023 · This review covers recent advances in the catalytic reduction of amides to amines without the need for metal catalysts, thus overcoming such problems.Missing: organocatalytic | Show results with:organocatalytic
[38]
Catalyzed Reductive Amination of Biomass-Derived Keto Acids to ...
Mar 31, 2023 · The two versatile reactions were triggered by an earth-abundant calcium-based catalyst using hydrosilane as a reducing reagent under solvent- ...
[39]
Engineered Biocatalysts for Enantioselective Reductive Aminations ...
Mar 22, 2023 · Here we show that the scope of reductive aminases (RedAms) can be extended to allow selective reductive aminations of cyclic secondary amines.Missing: amide | Show results with:amide
[40]
Deoxygenative photochemical alkylation of secondary amides ...
Jan 22, 2025 · Our method leverages triflic anhydride-mediated semi-reduction of amides to imines, followed by a photochemical radical alkylation step.