{ "id": "epvbgk8v6s", "slug": "hydroacylation", "title": "Hydroacylation", "updated": "2026-10-21", "topic_path": [ { "id": "physical", "label": "Physical world and mathematics", "api_url": "https://www.edgepedia.org/api/v1/topics/physical" }, { "id": "physical.chemistry", "label": "Chemistry", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry" }, { "id": "physical.chemistry.methods", "label": "Chemical principles and methods", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods" }, { "id": "physical.chemistry.methods.chemical-synthesis", "label": "Chemical synthesis", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods.chemical-synthesis" }, { "id": "physical.chemistry.methods.chemical-synthesis.named-preparative-methods", "label": "Named synthetic methods", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods.chemical-synthesis.named-preparative-methods" }, { "id": "physical.chemistry.methods.chemical-synthesis.named-preparative-methods.alpha-ho-to-z", "label": "Titles Ho to Z", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods.chemical-synthesis.named-preparative-methods.alpha-ho-to-z" } ], "geo": [ { "id": "geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis.named-preparative-methods", "label": "Non-geographic · 1946 to 2000: Named synthetic methods", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis.named-preparative-methods", "path": [ { "id": "geo.nongeo", "label": "Non-geographic", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo" }, { "id": "geo.nongeo.t1946", "label": "Non-geographic · 1946 to 2000", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946" }, { "id": "geo.nongeo.t1946.physical", "label": "Physical world and mathematics", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical" }, { "id": "geo.nongeo.t1946.physical.chemistry", "label": "Chemistry", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry" }, { "id": "geo.nongeo.t1946.physical.chemistry.methods", "label": "Chemical principles and methods", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods" }, { "id": "geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis", "label": "Chemical synthesis", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis" }, { "id": "geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis.named-preparative-methods", "label": "Named synthetic methods", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis.named-preparative-methods" } ] } ], "excerpt": "Hydroacylation is an organic reaction in which the formyl C–H bond of an aldehyde adds across an alkene or alkyne to give a ketone, typically catalyzed by transition-metal complexes such as rhodium.", "snippet": "Hydroacylation is an organic reaction in which the formyl C–H bond of an aldehyde adds across an alkene or alkyne to give a ketone, typically catalyzed by transition-metal complexes such as rhodium.", "node": "physical.chemistry.methods.chemical-synthesis.named-preparative-methods.alpha-ho-to-z", "markdown": "# Hydroacylation\n\nHydroacylation is an organic reaction in which the formyl C–H bond of an aldehyde adds across an unsaturated bond, most often an alkene or alkyne, to give a ketone; it is typically catalyzed by transition-metal complexes.\n\n| Key fact | Detail |\n|---|---|\n| Product | An aldehyde plus an alkene gives a ketone; intramolecular reactions of 4-pentenals give cyclopentanones[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC8486976/) |\n| Key intermediate | An acyl–Rh(III)–hydride formed by oxidative addition of the aldehyde C–H bond[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC8486976/) |\n| Main competing pathway | Tsuji–Wilkinson reductive decarbonylation to a Rh–carbonyl complex, which deactivates the catalyst[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC8486976/) |\n| Benchmark catalyst | 1 mol% [Rh(dppe)]BF₄ converts 4-pentenal to cyclopentanone in 95% yield with no decarbonylation[2](https://escholarship.org/content/qt31s4n3r4/qt31s4n3r4_noSplash_2f2e72ff1e2cafc7d340f96468408b40.pdf) |\n| Modern loadings | Small-bite-angle Rh bisphosphine systems run at 0.1 mol%[3](https://onlinelibrary.wiley.com/doi/10.1002/anie.201503208) |\n| Enantioselective scope | Rh–Josiphos ketone hydroacylation: 53–98% yields, 84–96% ee[4](https://doi.org/10.1021/ja504296x) |\n| Catalyst metals used | Rh, Co, Ru, Ir, and Ni, plus NHC and photocatalyst variants[5](https://pubs.rsc.org/en/content/articlehtml/2016/qo/c6qo00023a) • [6](https://pubs.acs.org/jacsat/article/148/35/37616/5336068/Catalytic-Hydroacylation-of-Alkynes-with-Aldehydes) |\n\n## How it works\n\nThe accepted mechanism for Rh-catalyzed olefin hydroacylation begins with oxidative addition of the aldehyde formyl C–H bond to a cationic Rh(I) center, generating an acyl–Rh(III)–hydride. The alkene then coordinates, migratory insertion into the Rh–H bond affords a linear or branched acyl–Rh(III)–alkyl species, and C–C reductive elimination releases the ketone and regenerates the catalyst.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC8486976/) In the Sakai-type description, alkene insertion into the Rh–H bond gives a 6-membered rhodacycle before reductive elimination.[7](https://www.jstage.jst.go.jp/article/cpb/63/6/63_c15-00135/_html/-char/en)\n\nDirect support for this pathway came from [David Milstein](https://www.edgepedia.org/david-milstein), who isolated a stable cis-hydridopentenoylrhodium(III) trimethylphosphine complex from oxidative addition of pent-4-enal to RhCl(PMe₃)₃ and observed its intramolecular hydroacylation to cyclopentanone.[8](https://doi.org/10.1039/c39820001357) Kinetic isotope effects locate the slow step, which varies by system: KIE values of 2.5 ± 0.2 (hydrocinnamaldehyde) and 2.4 ± 0.2 (2-naphthaldehyde) support irreversible, turnover-limiting aldehyde C–H oxidative addition in branched-selective alkene hydroacylation[9](https://pubs.rsc.org/en/content/articlehtml/2015/sc/c4sc02026j), a KIE of 1.5 ± 0.1 in β-amido-aldehyde/alkyne reactions instead supports turnover-limiting hydride insertion[10](https://ora.ox.ac.uk/objects/uuid:b04bb249-1811-4235-8148-0fa7b565e901/files/md5f83fec78a92f6702454759ca1d94e8), and in carbonyl hydroacylation a KIE of 1.79 ± 0.06 with DFT and Hammett studies points to ketone insertion into the Rh–H bond as turnover-limiting.[2](https://escholarship.org/content/qt31s4n3r4/qt31s4n3r4_noSplash_2f2e72ff1e2cafc7d340f96468408b40.pdf)\n\n## How it is done\n\nA typical intramolecular reaction combines an unsaturated aldehyde such as a 4-pentenal with a cationic Rh(I) diphosphine catalyst, for example [Rh(dppe)]BF₄ at 1 mol%, which converts 4-pentenal to cyclopentanone in 95% yield with no decarbonylation[2](https://escholarship.org/content/qt31s4n3r4/qt31s4n3r4_noSplash_2f2e72ff1e2cafc7d340f96468408b40.pdf); these cationic Rh catalysts enable room-temperature reactions.[11](https://pmc.ncbi.nlm.nih.gov/articles/PMC4456096/) Intermolecular reactions require a strategy to suppress decarbonylation: chelating aldehydes such as salicylaldehydes or β-S-aldehydes, or a transient directing group. With 2-amino-3-picoline as co-catalyst, the aldehyde forms a chelating picolyl imine that directs the metal and is hydrolyzed after reaction.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC8486976/) In β-amido-aldehyde alkyne hydroacylation, Rh–DPEPhos catalysts stabilize a 6-coordinate acyl hydride through a hemilabile Rh···O interaction, and running at 0.5 mol% loading with equimolar reagents gives essentially 100% selectivity for hydroacylation over alkyne cyclotrimerization.[10](https://ora.ox.ac.uk/objects/uuid:b04bb249-1811-4235-8148-0fa7b565e901/files/md5f83fec78a92f6702454759ca1d94e8) Excess alkene increases the rate of hydroacylation and disfavors decarbonylation.[12](https://www.lookchem.com/FreePDFArticle/1396756-72-1.htm)\n\nThe acyl–Rh(III)–hydride can undergo off-cycle reductive decarbonylation, the Tsuji–Wilkinson pathway, via a Rh–carbonyl complex plus alkane; this irreversible side reaction deactivates the catalyst, and attenuating it is central to robust catalyst systems.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC8486976/) • [10](https://ora.ox.ac.uk/objects/uuid:b04bb249-1811-4235-8148-0fa7b565e901/files/md5f83fec78a92f6702454759ca1d94e8) Early studies consequently used 5–10 mol% loadings and activated substrates.[3](https://onlinelibrary.wiley.com/doi/10.1002/anie.201503208) [Chelation](https://www.edgepedia.org/chelation) is a key remedy: salicylaldehydes, β-S-aldehydes, and quinoline aldehydes bind in ways that block decarbonylation, and Suggs showed that quinoline aldehydes couple to olefins instead of decarbonylating.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC8486976/) Hemilabile Rh···O stabilization of the 6-coordinate acyl hydride blocks the cis site needed for decarbonylation, at some cost in turnover.[10](https://ora.ox.ac.uk/objects/uuid:b04bb249-1811-4235-8148-0fa7b565e901/files/md5f83fec78a92f6702454759ca1d94e8) Ligand design helps too: the o-MeOC₆H₄ group on small-bite-angle bisphosphines increases the rate of olefin insertion into the Rh–H bond, keeping the acyl hydride concentration low.[5](https://pubs.rsc.org/en/content/articlehtml/2016/qo/c6qo00023a) Rh(III) catalysis that activates the aldehyde by concerted metalation–deprotonation bypasses the acylrhodium hydride entirely, preventing reductive decarbonylation.[2](https://escholarship.org/content/qt31s4n3r4/qt31s4n3r4_noSplash_2f2e72ff1e2cafc7d340f96468408b40.pdf)\n\n## Origin\n\nAldehyde C–H bonds undergo oxidative addition to generate acyl-metal-hydride species during studies on decarbonylation.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC8486976/) The first Rh-mediated intramolecular hydroacylation of 4-pentenals to cyclopentanones, en route to prostanoid intermediates, was reported by K. Sakai, J. Ide, O. Oda, and N. Nakamura in Tetrahedron Letters in 1972[13](https://doi.org/10.1016/s0040-4039%2801%2984569-x); it used stoichiometric [Wilkinson's catalyst](https://www.edgepedia.org/wilkinsons-catalyst) and gave only 30% of the cyclopentanone, the remainder being decarbonylation products.[14](https://digital.csic.es/bitstream/10261/217409/1/Barnhart%20et%20al..pdf) Charles F. Lochow and Roy G. Miller introduced the pendant-alkene chelation strategy in the [Journal of the American Chemical Society](https://www.edgepedia.org/journal-of-the-american-chemical-society) in 1976[15](https://doi.org/10.1021/ja00421a050), and R. C. Larock, K. Oertle, and G. F. Potter reported early catalytic Rh(I)-catalyzed cyclization of unsaturated aldehydes to cyclopentanones in 1980.[16](https://doi.org/10.1021/ja00521a031) The first asymmetric variant was reported by Brian R. James and Charles G. Young in 1983[17](https://doi.org/10.1039/c39830001215), giving α-quaternary cyclopentanones in 40–50% yields with ee up to 52% at 0.16 mol% Rh but 160 °C.[11](https://pmc.ncbi.nlm.nih.gov/articles/PMC4456096/) The breakthrough came in 1988, when [David P. Fairlie](https://www.edgepedia.org/david-p-fairlie) and B. Bosnich reported cationic Rh(I)-diphosphine catalysts that convert 4-pentenals to cyclopentanones efficiently[18](https://doi.org/10.1021/om00094a025), enabling room-temperature reactions at loadings as low as 1 mol%.[11](https://pmc.ncbi.nlm.nih.gov/articles/PMC4456096/)\n\n## Variants\n\nSince the 1972 report, alkene and alkyne hydroacylation has evolved to catalysts based on Rh, Co, Ru, Ir, and Ni, and also to N-heterocyclic carbenes and photocatalysts.[5](https://pubs.rsc.org/en/content/articlehtml/2016/qo/c6qo00023a) The intramolecular reaction forms rings, chiefly cyclopentanones; 5-Alkenals give 6-membered ketones in moderate yield even with 30 mol% Rh(I).[7](https://www.jstage.jst.go.jp/article/cpb/63/6/63_c15-00135/_html/-char/en) Intermolecular asymmetric variants couple salicylaldehydes with norbornadienes and norbornenes with ee up to 82%.[11](https://pmc.ncbi.nlm.nih.gov/articles/PMC4456096/) Carbonyl (ketone) hydroacylation includes 1,4-ketoaldehydes cyclizing to racemic γ-lactones, highly enantioselective carbonyl hydroacylation, and enantioselective intermolecular ketone hydroacylation, coupling aldehydes with ketoamides using a Rh–Josiphos catalyst.[4](https://doi.org/10.1021/ja504296x) • [1](https://pmc.ncbi.nlm.nih.gov/articles/PMC8486976/) Photoredox–Ni dual catalysis achieves chelation-free terminal alkyne hydroacylation[19](https://doi.org/10.1021/acs.orglett.2c03481), and photoredox cobalt/NHC cooperative triple catalysis gives branched-selective alkene hydroacylation.[20](https://doi.org/10.1021/acscatal.2c04970)\n\nAmong metals, cationic [Rh(diphosphine)]⁺ catalysts cyclize 4-pentenals at 25 °C with high turnover numbers, and with the binap catalyst give almost complete enantioselectivity for 4-substituted 4-pentenals bearing tertiary groups.[14](https://digital.csic.es/bitstream/10261/217409/1/Barnhart%20et%20al..pdf) Small-bite-angle systems [Rh(R₂PCH₂PR₂)(η⁶-C₆H₅F)][BArF₄] couple terminal and activated internal alkenes with β-substituted aldehydes at 0.1 mol%.[3](https://onlinelibrary.wiley.com/doi/10.1002/anie.201503208) Branched-selective hydroacylation of 2-vinylphenols with alkyl, alkenyl, and aryl aldehydes using [Rh(cod)OMe]₂ plus dcpm gives >20:1 branched-to-linear selectivity.[9](https://pubs.rsc.org/en/content/articlehtml/2015/sc/c4sc02026j) Cobalt catalysts hydroacylate aldehydes with 1,3-dienes through oxidative cyclization, endocyclic β-H elimination of a seven-membered cobaltacycle, and reductive elimination, giving allylic ketones in high yield while avoiding the acylmetal hydride and thus decarbonylation.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC8486976/) [Ruthenium](https://www.edgepedia.org/ruthenium) tandem RuHCl(CO)(PPh₃)/Josiphos catalysis gives β,γ-unsaturated ketones from alkynes in 61–95% yield, typically >20:1 rr[5](https://pubs.rsc.org/en/content/articlehtml/2016/qo/c6qo00023a), and Ru-catalyzed intermolecular hydroacylation and transhydroformylation of olefins with aldehydes was reported by Teruyuki Kondo and colleagues in 1990.[21](https://doi.org/10.1021/jo00291a035) Iridium [Ir(OH)(cod)]₂ systems hydroacylate bicyclic alkenes with salicylaldehydes in 91–99% yield with nearly perfect exo-selectivity[5](https://pubs.rsc.org/en/content/articlehtml/2016/qo/c6qo00023a), and NiH catalysis of 1,1-disubstituted allenes with carboxylic anhydrides gives tetrasubstituted olefins under base-free conditions.[22](https://doi.org/10.1016/j.checat.2023.100606)\n\n## Applications\n\nHydroacylation is a direct route to cyclopentanones and cyclohexanones and to 5- to 7-membered rings generally: 4,6-dienals give 7-membered rings, and a sequential hydroacylation/cycloisomerization cascade affords bicyclo[5.3.0]decenones stereoselectively, applied to the synthesis of epiglobulol.[7](https://www.jstage.jst.go.jp/article/cpb/63/6/63_c15-00135/_html/-char/en) Branched-selective 2-vinylphenol hydroacylation enabled short syntheses of four neolignan natural products via hydroacylation plus acid-catalyzed cyclocondensation.[9](https://pubs.rsc.org/en/content/articlehtml/2015/sc/c4sc02026j) [Salicylaldehyde](https://www.edgepedia.org/salicylaldehyde) derivatives couple with a wide range of unactivated alkenes at loadings as low as 2 mol% using the chiral phosphoramidite (R_a,R,R)-SIPHOS-PE, enabling syntheses of eight octaketide natural products including cytosporone B, and the Dong group prepared (S)-3-n-butylphthalide in 93% yield and 97% ee by ketone hydroacylation.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC8486976/)\n\n## Limitations and alternatives\n\nThe dominant failure mode is decarbonylation, which consumes both aldehyde and catalyst.[10](https://ora.ox.ac.uk/objects/uuid:b04bb249-1811-4235-8148-0fa7b565e901/files/md5f83fec78a92f6702454759ca1d94e8) Intermolecular aldehyde–ketone cross-coupling is considerably more challenging because of competing decarbonylation, Tishchenko dimerization, and aldol pathways; a CO atmosphere is occasionally used to suppress decarbonylation in low-valent Ru systems.[2](https://escholarship.org/content/qt31s4n3r4/qt31s4n3r4_noSplash_2f2e72ff1e2cafc7d340f96468408b40.pdf) Remaining challenges include medium- and large-ring intramolecular reactions without stabilizing functional groups, a broader intermolecular substrate scope, and cheaper catalysts to replace rhodium bisphosphine complexes.[5](https://pubs.rsc.org/en/content/articlehtml/2016/qo/c6qo00023a)\n\nRecent work addresses the cost and scope problems with base metals and light. Ji, Li, and Zhang at Wuhan University reported dual photo/cobalt-catalyzed anti-Markovnikov hydroacylation of aryl alkenes with aldehydes, using TBADT as photocatalyst and 385 nm LEDs, with the key step being cobalt-catalyzed hydrogen atom transfer[23](https://pubs.acs.org/doi/10.1021/acs.orglett.4c04373); the same group reported direct ketone synthesis from primary alcohols and alkenes by dual photo/cobalt catalysis in [Nature Communications](https://www.edgepedia.org/nature-communications) in 2024.[24](https://doi.org/10.1038/s41467-024-51190-3)\n\n## References\n\n1. [Teaching Aldehydes New Tricks Using Rhodium- and Cobalt-Hydride Catalysis (Dong group Account, Accounts of Chemical Research)](https://pmc.ncbi.nlm.nih.gov/articles/PMC8486976/)\n2. [Transition Metal Catalyzed Hydroacylation (UC eScholarship review chapter)](https://escholarship.org/content/qt31s4n3r4/qt31s4n3r4_noSplash_2f2e72ff1e2cafc7d340f96468408b40.pdf)\n3. [Well-Defined and Robust Rhodium Catalysts for the Hydroacylation of Terminal and Internal Alkenes](https://onlinelibrary.wiley.com/doi/10.1002/anie.201503208)\n4. [Kevin G. M. Kou, Diane N. Le, Vy M. Dong (2014). Rh(I)-Catalyzed Intermolecular Hydroacylation: Enantioselective Cross-Coupling of Aldehydes and Ketoamides. Journal of the American Chemical Society.](https://doi.org/10.1021/ja504296x)\n5. [Recent advances in transition metal-catalysed hydroacylation of alkenes and alkynes](https://pubs.rsc.org/en/content/articlehtml/2016/qo/c6qo00023a)\n6. [Catalytic Hydroacylation of Alkynes with Aldehydes by a Cp′Mo Catalyst | Journal of the American Chemical Society | ACS Publications](https://pubs.acs.org/jacsat/article/148/35/37616/5336068/Catalytic-Hydroacylation-of-Alkynes-with-Aldehydes)\n7. [Development of Novel Cyclizations via Rhodacycle Intermediate and Its Application to Synthetic Organic Chemistry](https://www.jstage.jst.go.jp/article/cpb/63/6/63_c15-00135/_html/-char/en)\n8. [David Milstein (1982). Isolation and direct observation of intramolecular hydroacylation of a cis-hydridopent-4-enoylrhodium(III) complex. Journal of the Chemical Society Chemical Communications.](https://doi.org/10.1039/c39820001357)\n9. [Mechanistic insights into hydroacylation with non-chelating aldehydes](https://pubs.rsc.org/en/content/articlehtml/2015/sc/c4sc02026j)\n10. [Mechanistic study of intermolecular alkyne hydroacylation with β-amido-aldehydes (Oxford ORA manuscript, Willis/Weller groups)](https://ora.ox.ac.uk/objects/uuid:b04bb249-1811-4235-8148-0fa7b565e901/files/md5f83fec78a92f6702454759ca1d94e8)\n11. [Enantioselective Rh-Catalyzed Hydroacylation of Olefins: From Serendipitous Discovery to Rational Design](https://pmc.ncbi.nlm.nih.gov/articles/PMC4456096/)\n12. [Rhodium-Phosphoramidite Catalyzed Alkene Hydroacylation: Mechanism and Octaketide Natural Product Synthesis (von Delius, Le, Dong, JACS 2012)](https://www.lookchem.com/FreePDFArticle/1396756-72-1.htm)\n13. [Synthetic studies on prostanoids 1 synthesis of methyl 9-oxoprostanoate (Tetrahedron Letters, 1972)](https://doi.org/10.1016/s0040-4039%2801%2984569-x)\n14. [Asymmetric Catalysis. Asymmetric Catalytic Intramolecular Hydroacylation of 4-Pentenals Using Chiral Rhodium Diphosphine Catalysts](https://digital.csic.es/bitstream/10261/217409/1/Barnhart%20et%20al..pdf)\n15. [Charles F. Lochow, Roy G. Miller (1976). Transition-metal-promoted aldehyde-alkene addition reactions. Journal of the American Chemical Society.](https://doi.org/10.1021/ja00421a050)\n16. [R. C. Larock, K. Oertle, G. F. Potter (1980). A convenient synthesis of cyclopentanones via rhodium(I)-catalyzed intramolecular hydroacylation of unsaturated aldehydes. Journal of the American Chemical Society.](https://doi.org/10.1021/ja00521a031)\n17. [Brian R. James, Charles G. Young (1983). The asymmetric cyclisation of substituted pent-4-enals by a chiral rhodium phosphine catalyst. Journal of the Chemical Society Chemical Communications.](https://doi.org/10.1039/c39830001215)\n18. [David P. Fairlie, B. Bosnich (1988). Homogeneous catalysis. Conversion of 4-pentenals to cyclopentanones by efficient rhodium-catalyzed hydroacylation. Organometallics.](https://doi.org/10.1021/om00094a025)\n19. [Vetrivelan Murugesan and colleagues (2022). Photoredox–Ni Dual Catalysis: Chelation-Free Hydroacylation of Terminal Alkynes. Organic Letters.](https://doi.org/10.1021/acs.orglett.2c03481)\n20. [Xiangzhang Tao and colleagues (2022). Branched-Selective Hydroacylation of Alkenes via Photoredox Cobalt and N -Heterocyclic Carbene Cooperative Triple Catalysis. ACS Catalysis.](https://doi.org/10.1021/acscatal.2c04970)\n21. [Teruyuki Kondo and colleagues (1990). Ruthenium complex catalyzed intermolecular hydroacylation and transhydroformylation of olefins with aldehydes. The Journal of Organic Chemistry.](https://doi.org/10.1021/jo00291a035)\n22. [Base-free NiH-catalyzed regio- and stereo-selective hydroacylation of allenes: A new route to synthesis of tetra-substituted olefins (Chem Catalysis, 2023)](https://doi.org/10.1016/j.checat.2023.100606)\n23. [Anti-Markovnikov Hydroacylation of Aryl Alkenes with Aldehydes Enabled by Photo/Cobalt Dual Catalysis (Org. Lett. 2025, 27, 334–339)](https://pubs.acs.org/doi/10.1021/acs.orglett.4c04373)\n24. [Guanghao Ji, Xinqiang Chen, Jing Zhang (2024). Direct ketone synthesis from primary alcohols and alkenes enabled by a dual photo/cobalt catalysis. Nature Communications.](https://doi.org/10.1038/s41467-024-51190-3)\n\n---\n*Topic: Encyclopedia › Physical world and mathematics › Chemistry › Chemical principles and methods › Chemical synthesis › Named synthetic methods › Titles Ho to Z*\n\n*Initially written Sep 29, 2026 · Edited: Oct 15, 2026; Oct 21, 2026*\n\n*Copyright 2026 EdgeChat AI, a subsidiary of Biostate AI.*\n\nLicense: Edgepedia Community License 1.0, https://www.edgepedia.org/edgepedia/license\n", "same_as": [], "url": "https://www.edgepedia.org/hydroacylation", "markdown_url": "https://www.edgepedia.org/hydroacylation.md", "license": { "name": "Edgepedia Community License 1.0", "url": "https://www.edgepedia.org/edgepedia/license", "summary": "Free with credit, commercial use included. AI training is open to everyone. For other uses, organizations over USD 100M in revenue or 100M monthly users license separately.", "spdx": "LicenseRef-Edgepedia-Community-1.0" }, "credit": "\"Hydroacylation\", Edgepedia (EdgeChat), https://www.edgepedia.org/hydroacylation. Edgepedia Community License 1.0.", "credit_md": "\"[Hydroacylation](https://www.edgepedia.org/hydroacylation)\", Edgepedia (EdgeChat), [https://www.edgepedia.org/hydroacylation](https://www.edgepedia.org/hydroacylation). [Edgepedia Community License 1.0](https://www.edgepedia.org/edgepedia/license).", "credit_html": "\"Hydroacylation\", Edgepedia (EdgeChat), https://www.edgepedia.org/hydroacylation. Edgepedia Community License 1.0.", "speakable": "Hydroacylation is an organic reaction in which the formyl C–H bond of an aldehyde adds across an alkene or alkyne to give a ketone, typically catalyzed by transition-metal complexes such as rhodium." }