Abstract
To create a circular plastics economy, new polymers are being developed that can be chemically recycled. Circular polyesters are of particular interest and to this end, lactones are ideal monomers. This Review examines catalytic routes to convert diols, hydroxy acids, and dicarboxylic acids to lactones, focusing on the development of scalable, atom-economic, and energy-efficient conversions of bio-derived feedstocks. Free energy analysis is used to inform process choices, such as reactor type, reaction phase, and use of solvent. Catalyst design principles are summarized for both direct (bio-substrate to lactone) and indirect (bio-substrate to intermediate to lactone) routes. Finally, we summarize literature that shows that many lactone precursors are readily accessible from various metabolic and chemo-catalytic pathways. Transitioning to bio-based monomers offers an opportunity to reduce reliance on fossil carbon resources, but requires advanced catalytic processes informed by mechanistic insights.

This is a preview of subscription content, access via your institution
Access options
Access Nature and 54 other Nature Portfolio journals
Get Nature+, our best-value online-access subscription
$32.99 / 30 days
cancel any time
Subscribe to this journal
Receive 12 digital issues and online access to articles
$119.00 per year
only $9.92 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to the full article PDF.
USD 39.95
Prices may be subject to local taxes which are calculated during checkout








References
Bachmann, M. et al. Towards circular plastics within planetary boundaries. Nat. Sustain. 6, 599–610 (2023).
Zhu, J.-B., Watson, E. M., Tang, J. & Chen, E. Y.-X. A synthetic polymer system with repeatable chemical recyclability. Science 360, 398–403 (2018).
Shi, C. et al. Design principles for intrinsically circular polymers with tunable properties. Chem 7, 2896–2912 (2021).
Luo, X. et al. Circularly recyclable polymers featuring topochemically weakened carbon–carbon bonds. J. Am. Chem. Soc. 144, 16588–16597 (2022).
Helms, B. A. Polydiketoenamines for a circular plastics economy. Acc. Chem. Res. 55, 2753–2765 (2022).
Eck, M. & Mecking, S. Closed-loop recyclable and nonpersistent polyethylene-like polyesters. Acc. Chem. Res. 57, 971–980 (2024).
Haque, F. M. et al. Defining the macromolecules of tomorrow through synergistic sustainable polymer research. Chem. Rev. 122, 6322–6373 (2022).
Zhu, Y., Romain, C. & Williams, C. K. Sustainable polymers from renewable resources. Nature 540, 354–362 (2016).
Shi, C., Quinn, E. C., Diment, W. T. & Chen, E. Y. X. Recyclable and (bio)degradable polyesters in a circular plastics economy. Chem. Rev. 124, 4393–4478 (2024).
Coates, G. W. & Getzler, Y. D. Y. L. Chemical recycling to monomer for an ideal, circular polymer economy. Nat. Rev. Mater. 5, 501–516 (2020).
Ellis, L. D. et al. Chemical and biological catalysis for plastics recycling and upcycling. Nat. Catal. 4, 539–556 (2021).
Rahimi, A. & García, J. M. Chemical recycling of waste plastics for new materials production. Nat. Rev. Chem. 1, 0046 (2017).
Zhang, Z., Gowda, R. R. & Chen, E. Y. X. Chemosynthetic P4HB: a ten-year journey from a ‘non-polymerizable’ monomer to a high-performance biomaterial. Acc. Mater. Res. 5, 1340–1352 (2024).
Nicholson, S. R., Rorrer, N. A., Carpenter, A. C. & Beckham, G. T. Manufacturing energy and greenhouse gas emissions associated with plastics consumption. Joule 5, 673–686 (2021).
Zhou, L. et al. Chemically circular, mechanically tough, and melt-processable polyhydroxyalkanoates. Science 380, 64–69 (2023).
Zhou, Z., LaPointe, A. M., Shaffer, T. D. & Coates, G. W. Nature-inspired methylated polyhydroxybutyrates from C1 and C4 feedstocks. Nat. Chem. 15, 856–861 (2023).
Kim, M. S. et al. A review of biodegradable plastics: chemistry, applications, properties, and future research needs. Chem. Rev. 123, 9915–9939 (2023).
Tang, X. & Chen, E. Y. X. Chemical synthesis of perfectly isotactic and high melting bacterial poly(3-hydroxybutyrate) from bio-sourced racemic cyclic diolide. Nat. Commun. 9, 2345 (2018).
Ritz, J., Fuchs, H., Kieczka, H. & Moran, W. C. in Ullmann’s Encyclopedia of Industrial Chemistry (Wiley, 2000).
Jochen, H. et al. Dehydrogenation of 1,4-butanediol to γ-butyrolactone. US patent, 5955620A (1999).
Young, F. G. & Fitzpatrick, J. T. β-Hydroxycarboxylic acids and lactones. US patent 2,580,714 (1952).
Sixt, J. β-Butyrolactone from diketene. US patent 2,763,664 (1956).
Luinstra, G., Molnar, F., Rieger, B. & Allmendinger, M. Catalyst and procedure for the carbonylation of oxiranes. DE10235317 (2004).
Stadler, B. M., Wulf, C., Werner, T., Tin, S. & de Vries, J. G. Catalytic approaches to monomers for polymers based on renewables. ACS Catal. 9, 8012–8067 (2019).
Huo, J. & Shanks, B. H. Bioprivileged molecules: integrating biological and chemical catalysis for biomass conversion. Annu. Rev. Chem. Biomol. Eng. 11, 63–85 (2020).
Kramer, J. W., Lobkovsky, E. B. & Coates, G. W. Practical β-lactone synthesis: epoxide carbonylation at 1 atm. Org. Lett. 8, 3709–3712 (2006).
Kramer, J. W., Rowley, J. M. & Coates, G. W. Organic Reactions 1–104 (Wiley, 2015).
Park, H. D., Dincă, M. & Román-Leshkov, Y. Heterogeneous epoxide carbonylation by cooperative ion-pair catalysis in Co(CO)4−-incorporated Cr-MIL-101. ACS Cent. Sci. 3, 444–448 (2017).
Tran, V. G. et al. An end-to-end pipeline for succinic acid production at an industrially relevant scale using Issatchenkia orientalis. Nat. Commun. 14, 6152 (2023).
Han, T., Kim, G. B. & Lee, S. Y. Glutaric acid production by systems metabolic engineering of an l-lysine-overproducing Corynebacterium glutamicum. Proc. Natl Acad. Sci. USA 117, 30328–30334 (2020).
Choi, S., Kim, H. U., Kim, T. Y. & Lee, S. Y. Systematic engineering of TCA cycle for optimal production of a four-carbon platform chemical 4-hydroxybutyric acid in Escherichia coli. Metab. Eng. 38, 264–273 (2016).
Sohn, Y. J. et al. Fermentative high-level production of 5-hydroxyvaleric acid by metabolically engineered Corynebacterium glutamicum. ACS Sustain. Chem. Eng. 9, 2523–2533 (2021).
Ewell, R. H. & Eyring, H. Theory of the viscosity of liquids as a function of temperature and pressure. J. Chem. Phys. 5, 726–736 (1937).
Chen, S.-C., Hsu, L.-A., Lin, F.-S. & Tsai, C.-L. Method for preparing lactone. European Patent EP1214972A1 (2000).
Touchy, A. S. & Shimizu, K.-I. Acceptorless dehydrogenative lactonization of diols by Pt-loaded SnO2 catalysts. RSC Adv. 5, 29072–29075 (2015).
Zhong, W., Liu, H., Bai, C., Liao, S. & Li, Y. Base-free oxidation of alcohols to esters at room temperature and atmospheric conditions using nanoscale co-based catalysts. ACS Catal. 5, 1850–1856 (2015).
Eagan, N. M., Kumbhalkar, M. D., Buchanan, J. S., Dumesic, J. A. & Huber, G. W. Chemistries and processes for the conversion of ethanol into middle-distillate fuels. Nat. Rev. Chem. 3, 223–249 (2019).
Kim, T. Y. et al. Gas-phase dehydration of vicinal diols to epoxides: dehydrative epoxidation over a Cs/SiO2 catalyst. J. Catal. 323, 85–99 (2015).
Kostal, J. & Jorgensen, W. L. Thorpe−Ingold acceleration of oxirane formation is mostly a solvent effect. J. Am. Chem. Soc. 132, 8766–8773 (2010).
Zhou, L. et al. Chain-end controlled depolymerization selectivity in α,α-disubstituted propionate PHAs with dual closed-loop recycling and record-high melting temperature. J. Am. Chem. Soc. 146, 29895–29904 (2024).
Badlani, M. & Wachs, I. E. Methanol: a ‘smart’ chemical probe molecule. Catal. Lett. 75, 137–149 (2001).
Duan, H., Yamada, Y., Kubo, S. & Sato, S. Vapor-phase catalytic dehydration of 2,3-butanediol to 3-buten-2-ol over ZrO2 modified with alkaline earth metal oxides. Appl. Catal. A Gen. 530, 66–74 (2017).
Burcham, L. J., Badlani, M. & Wachs, I. E. The origin of the ligand effect in metal oxide catalysts: novel fixed-bed in situ infrared and kinetic studies during methanol oxidation. J. Catal. 203, 104–121 (2001).
Zhang, B., Ford, M. E., Ream, E. & Wachs, I. E. Olefin metathesis over supported MoOx catalysts: influence of the oxide support. Catal. Sci. Technol. 13, 217–225 (2023).
Kiani, D. & Baltrusaitis, J. A spectroscopic study of supported-phosphate-catalysts (SPCs): evidence of surface-mediated hydrogen-transfer. ChemCatChem 13, 2064–2073 (2021).
Zhang, W., Yu, D., Ji, X. & Huang, H. Efficient dehydration of bio-based 2,3-butanediol to butanone over boric acid modified HZSM-5 zeolites. Green Chem. 14, 3441–3450 (2012).
Ramayya, S., Brittain, A., DeAlmeida, C., Mok, W. & Antal, M. J. Acid-catalysed dehydration of alcohols in supercritical water. Fuel 66, 1364–1371 (1987).
Jung, M. E. & Piizzi, G. Gem-disubstituent effect: theoretical basis and synthetic applications. Chem. Rev. 105, 1735–1766 (2005).
Grant, J. T., Carrero, C. A., Love, A. M., Verel, R. & Hermans, I. Enhanced two-dimensional dispersion of group V metal oxides on silica. ACS Catal. 5, 5787–5793 (2015).
Kiani, D., Sourav, S., Wachs, I. E. & Baltrusaitis, J. Synthesis and molecular structure of model silica-supported tungsten oxide catalysts for oxidative coupling of methane (OCM). Catal. Sci. Technol. 10, 3334–3345 (2020).
Kiani, D. et al. Existence and properties of isolated catalytic sites on the surface of β-cristobalite-supported, doped tungsten oxide catalysts (WOx/β-SiO2, Na-WOx/β-SiO2, Mn-WOx/β-SiO2) for oxidative coupling of methane (OCM): a combined periodic DFT and experimental study. ACS Catal. 10, 4580–4592 (2020).
Hou, S., Cao, Y., Xiong, W., Liu, H. & Kou, Y. Site requirements for the oxidative coupling of methane on SiO2-supported Mn catalysts. Ind. Eng. Chem. Res. 45, 7077–7083 (2006).
Kiani, D., Sourav, S., Baltrusaitis, J. & Wachs, I. E. Oxidative coupling of methane (OCM) by SiO2-supported tungsten oxide catalysts promoted with Mn and Na. ACS Catal. 9, 5912–5928 (2019).
Jiang, J. & Yoon, S. A metalated porous porphyrin polymer with [Co(CO)4]− anion as an efficient heterogeneous catalyst for ring expanding carbonylation. Sci. Rep. 8, 13243 (2018).
Rajendiran, S., Natarajan, P. & Yoon, S. A covalent triazine framework-based heterogenized Al–Co bimetallic catalyst for the ring-expansion carbonylation of epoxide to β-lactone. RSC Adv. 7, 4635–4638 (2017).
Park, H. D., Dincă, M. & Román-Leshkov, Y. Continuous-flow production of succinic anhydrides via catalytic β-lactone carbonylation by Co(CO)4⊂Cr-MIL-101. J. Am. Chem. Soc. 140, 10669–10672 (2018).
Ichikawa, N., Sato, S., Takahashi, R., Sodesawa, T. & Inui, K. Dehydrogenative cyclization of 1,4-butanediol over copper-based catalyst. J. Mol. Catal. A Chem. 212, 197–203 (2004).
Nagaiah, P. et al. Selective vapour phase dehydrogenation of biomass-derived 1,4-butanediol to gamma butyrolactone over Cu/ZrO2 catalysts: influence of La2O3 promotor. Res. Chem. Intermed. 44, 5817–5831 (2018).
Chong, S. et al. Enhanced the dehydrocyclization of 1,4-butanediol to γ-butyrolactone via the regulation of interface oxygen vacancies in Cu/MgO-CeO2 catalyst. Chem. Eng. J. 489, 151366 (2024).
Huang, J., Wang, Y., Zheng, J., Dai, W.-L. & Fan, K. Influence of support surface basicity and gold particle size on catalytic activity of Au/γ-AlOOH and Au/γ-Al2O3 catalyst in aerobic oxidation of α,ω-diols to lactones. Appl. Catal. B Environ. 103, 343–350 (2011).
Huang, J., Dai, W.-L., Li, H. & Fan, K. Au/TiO2 as high efficient catalyst for the selective oxidative cyclization of 1,4-butanediol to γ-butyrolactone. J. Catal. 252, 69–76 (2007).
Jarvis, J. S. et al. Inhibiting the dealkylation of basic arenes during n-alkane direct aromatization reactions and understanding the C6 ring closure mechanism. ACS Catal. 10, 8428–8443 (2020).
Miller, J. T., Agrawal, N. G. B., Lane, G. S. & Modica, F. S. Effect of pore geometry on ring closure selectivities in platinum L-zeolite dehydrocyclization catalysts. J. Catal. 163, 106–116 (1996).
Huang, J., Dai, W.-L. & Fan, K. Support effect of new Au/FeOx catalysts in the oxidative dehydrogenation of α,ω-diols to lactones. J. Phys. Chem. C 112, 16110–16117 (2008).
Chen, A. et al. Structure of the catalytically active copper–ceria interfacial perimeter. Nat. Catal. 2, 334–341 (2019).
Li, X. et al. Ethanol dehydrogenation to acetaldehyde over a Cuδ+-based Cu-MFI catalyst. Chin. J. Catal. 49, 91–101 (2023).
Hanukovich, S., Dang, A. & Christopher, P. Influence of metal oxide support acid sites on Cu-catalyzed nonoxidative dehydrogenation of ethanol to acetaldehyde. ACS Catal. 9, 3537–3550 (2019).
Wang, C. et al. Low-temperature dehydrogenation of ethanol on atomically dispersed gold supported on ZnZrOx. ACS Catal. 6, 210–218 (2016).
Farnesi Camellone, M. & Marx, D. Nature and role of activated molecular oxygen species at the gold/titania interface in the selective oxidation of alcohols. J. Phys. Chem. C 118, 20989–21000 (2014).
Yi, N., Si, R., Saltsburg, H. & Flytzani-Stephanopoulos, M. Active gold species on cerium oxide nanoshapes for methanol steam reforming and the water gas shift reactions. Energy Environ. Sci. 3, 831–837 (2010).
Wang, T. et al. Nature of metal–support interaction for metal catalysts on oxide supports. Science 386, 915–920 (2024).
Wu, P. et al. Harnessing strong metal–support interactions via a reverse route. Nat. Commun. 11, 3042 (2020).
van Deelen, T. W., Hernández Mejía, C. & de Jong, K. P. Control of metal–support interactions in heterogeneous catalysts to enhance activity and selectivity. Nat. Catal. 2, 955–970 (2019).
Xie, J. et al. Deactivation of supported Pt catalysts during alcohol oxidation elucidated by spectroscopic and kinetic analyses. ACS Catal. 7, 6745–6756 (2017).
Wei, Z., Karim, A., Li, Y. & Wang, Y. Elucidation of the roles of re in aqueous-phase reforming of glycerol over Pt–Re/C Catalysts. ACS Catal. 5, 7312–7320 (2015).
Galley, R. Processes for the manufacture of lactones. WO2002016346 (2002).
Wu, X., Guo, J., Lv, W. & Jia, Z. Green preparation of four-membered ring beta-lactones. CN116283840 (2023).
Whittingham, M. S. Solid-state ionics: the key to the discovery and domination of lithium batteries: some learnings from β-alumina and titanium disulfide. MRS Bull. 46, 168–173 (2021).
You, C., Zhang, C., Chen, L. & Qi, Z. Highly dispersed palladium nanoclusters incorporated in amino-functionalized silica spheres for the selective hydrogenation of succinic acid to γ-butyrolactone. Appl. Organomet. Chem. 29, 653–660 (2015).
Le, S. D. & Nishimura, S. Highly selective synthesis of 1,4-butanediol via hydrogenation of succinic acid with supported Cu–Pd alloy nanoparticles. ACS Sustain. Chem. Eng. 7, 18483–18492 (2019).
Tapin, B. et al. Study of monometallic Pd/TiO2 catalysts for the hydrogenation of succinic acid in aqueous phase. ACS Catal. 3, 2327–2335 (2013).
Zhang, C., Chen, L., Cheng, H., Zhu, X. & Qi, Z. Atomically dispersed Pd catalysts for the selective hydrogenation of succinic acid to γ-butyrolactone. Catal. Today 276, 55–61 (2016).
Heisig, C., Diedenhoven, J., Jensen, C., Gehrke, H. & Turek, T. Selective hydrogenation of biomass-derived succinic acid: reaction network and kinetics. Chem. Eng. Technol. 43, 484–492 (2020).
Hayes, G. et al. Polymers without petrochemicals: sustainable routes to conventional monomers. Chem. Rev. 123, 2609–2734 (2023).
Abou Hamdan, M., Loridant, S., Jahjah, M., Pinel, C. & Perret, N. TiO2-supported molybdenum carbide: an active catalyst for the aqueous phase hydrogenation of succinic acid. Appl. Catal. A Gen. 571, 71–81 (2019).
Hamdan, M. A. et al. Influence of reduction–carburization parameters on the performance of supported molybdenum carbide catalysts in succinic acid hydrogenation. Ind. Eng. Chem. Res. 59, 12964–12976 (2020).
Khusnutdinov, R. I., Shchadneva, N. A., Baiguzina, A. R., Lavrentieva, Y. Y. & Dzhemilev, U. M. Generation of alkyl hypochlorites in oxidation of alcohols with carbon tetrachloride catalyzed by vanadium and manganese compounds. Russ. Chem. Bull. 51, 2074–2079 (2002).
Bhatia, A., Kannan, M. & Muthaiah, S. Ruthenium-promoted acceptorless and oxidant-free lactone synthesis in aqueous medium. Synlett 30, 721–725 (2019).
Tanzawa, T. & Schwartz, J. Catalytic conversion of beta-hydroxy carboxylic acids to olefins by tungsten(VI) complexes: a new acyl group transfer catalyst. Organometallics 9, 3026–3027 (1990).
Zhuang, Z. & Yu, J.-Q. Lactonization as a general route to β-C(sp3)–H functionalization. Nature 577, 656–659 (2020).
Molnar, F., Luinstra, G. A., Allmendinger, M. & Rieger, B. Multisite catalysis: a mechanistic study of β-lactone synthesis from epoxides and CO — insights into a difficult case of homogeneous catalysis. Chem. Eur. J. 9, 1273–1280 (2003).
Church, T. L., Getzler, Y. D. Y. L. & Coates, G. W. The mechanism of epoxide carbonylation by [Lewis acid]+[Co(CO)4]− catalysts. J. Am. Chem. Soc. 128, 10125–10133 (2006).
Schmidt, J. A. R., Lobkovsky, E. B. & Coates, G. W. Chromium(III) octaethylporphyrinato tetracarbonylcobaltate: a highly active, selective, and versatile catalyst for epoxide carbonylation. J. Am. Chem. Soc. 127, 11426–11435 (2005).
Schmidt, J. A. R., Mahadevan, V., Getzler, Y. D. Y. L. & Coates, G. W. A readily synthesized and highly active epoxide carbonylation catalyst based on a chromium porphyrin framework: expanding the range of available β-lactones. Org. Lett. 6, 373–376 (2004).
Mahadevan, V., Getzler, Y. D. Y. L. & Coates, G. W. [Lewis acid]+[Co(CO)4]− complexes: a versatile class of catalysts for carbonylative ring expansion of epoxides and aziridines. Angew. Chem. Int. Ed. 41, 2781–2784 (2002).
Getzler, Y. D. Y. L., Mahadevan, V., Lobkovsky, E. B. & Coates, G. W. Synthesis of β-lactones: a highly active and selective catalyst for epoxide carbonylation. J. Am. Chem. Soc. 124, 1174–1175 (2002).
Rowley, J. M., Lobkovsky, E. B. & Coates, G. W. Catalytic double carbonylation of epoxides to succinic anhydrides: catalyst discovery, reaction scope, and mechanism. J. Am. Chem. Soc. 129, 4948–4960 (2007).
Linger, J. G. et al. Lignin valorization through integrated biological funneling and chemical catalysis. Proc. Natl Acad. Sci. USA 111, 12013–12018 (2014).
Pitzalis, M. F. & Sadler, J. C. Chemical bio-manufacture from diverse C-rich waste polymeric feedstocks using engineered microorganisms. RSC Sustain. 3, 1672–1684 (2025).
Sullivan, K. P. et al. Mixed plastics waste valorization through tandem chemical oxidation and biological funneling. Science 378, 207–211 (2022).
Wu, X., De Bruyn, M. & Barta, K. Deriving high value products from depolymerized lignin oil, aided by (bio)catalytic funneling strategies. Chem. Commun. 59, 9929–9951 (2023).
Delidovich, I. et al. Alternative monomers based on lignocellulose and their use for polymer production. Chem. Rev. 116, 1540–1599 (2016).
Cen, X., Dong, Y., Liu, D. & Chen, Z. New pathways and metabolic engineering strategies for microbial synthesis of diols. Curr. Opin. Biotechnol. 78, 102845 (2022).
Lee, S. Y. et al. A comprehensive metabolic map for production of bio-based chemicals. Nat. Catal. 2, 18–33 (2019).
Jang, W. D., Kim, G. B. & Lee, S. Y. An interactive metabolic map of bio-based chemicals. Trends Biotechnol. 41, 10–14 (2023).
Giarola, S., Romain, C., Williams, C. K., Hallett, J. P. & Shah, N. in Computer Aided Chemical Engineering Vol. 37 (eds Krist, V. G. et al.) 2561–2566 (Elsevier, 2015).
Zhang, L. et al. Highly selective hydrogenation of phthalic anhydride to phthalide over CoSix/CNTs catalyst prepared by multi-step microwave-assisted chemical vapor deposition. Mater. Chem. Phys. 180, 89–96 (2016).
Mahmoud, E., Watson, D. A. & Lobo, R. F. Renewable production of phthalic anhydride from biomass-derived furan and maleic anhydride. Green Chem. 16, 167–175 (2014).
Yuan, L. et al. Production of copolyester monomers from plant-based acrylate and acetaldehyde. Angew. Chem. Int. Ed. 61, e202113471 (2022).
Hu, Y. et al. Synthesis of 1,4-cyclohexanedimethanol, 1,4-cyclohexanedicarboxylic acid and 1,2-cyclohexanedicarboxylates from formaldehyde, crotonaldehyde and acrylate/fumarate. Angew. Chem. Int. Ed. 57, 6901–6905 (2018).
Chokhawala, H. A high yield route for the production of compounds from renewable sources. Europe patent 3047030A2 (2014).
He, J. et al. Synthesis of 1,6-hexanediol from cellulose derived tetrahydrofuran-dimethanol with Pt-WOx/TiO2 catalysts. ACS Catal. 8, 1427–1439 (2018).
Buntara, T. et al. Caprolactam from renewable resources: catalytic conversion of 5-hydroxymethylfurfural into caprolactone. Angew. Chem. Int. Ed. 50, 7083–7087 (2011).
Burt, S. P. et al. Production of 1,6-hexanediol from tetrahydropyran-2-methanol by dehydration–hydration and hydrogenation. Green Chem. 19, 1390–1398 (2017).
Liu, Y., Cen, X., Liu, D. & Chen, Z. Metabolic engineering of Escherichia coli for high-yield production of (R)-1,3-butanediol. ACS Synth. Biol. 10, 1946–1955 (2021).
Islam, T., Nguyen-Vo, T. P., Gaur, V. K., Lee, J. & Park, S. Metabolic engineering of Escherichia coli for biological production of 1, 3-butanediol. Bioresour. Technol. 376, 128911 (2023).
Barton, N. R. et al. An integrated biotechnology platform for developing sustainable chemical processes. J. Ind. Microbiol. Biotechnol. 42, 349–360 (2015).
Cargill to build biobased 1,4-butanediol plant. C&EN Global Enterprise https://doi.org/10.1021/cen-09922-buscon2 (2021).
GENOMATICA TO GO PUBLIC. Chemical & Engineering News Archive https://doi.org/10.1021/cen-v089n035.p008a (2011).
Rohles, C. M. et al. A bio-based route to the carbon-5 chemical glutaric acid and to bionylon-6,5 using metabolically engineered Corynebacterium glutamicum. Green Chem. 20, 4662–4674 (2018).
Huang, K. et al. Conversion of furfural to 1,5-pentanediol: process synthesis and analysis. ACS Sustain. Chem. Eng. 5, 4699–4706 (2017).
Brentzel, Z. J. et al. Chemicals from biomass: combining ring-opening tautomerization and hydrogenation reactions to produce 1,5-pentanediol from furfural. ChemSusChem 10, 1351–1355 (2017).
Dastidar, R. G. et al. Catalytic production of δ-valerolactone (DVL) from biobased 2-hydroxytetrahydropyran (HTHP) — combined experimental and modeling study. Appl. Catal. B Environ. Energy 360, 124519 (2025).
Acknowledgements
Funding was provided by the US Department of Energy, Office of Energy Efficiency and Renewable Energy, Advanced Materials and Manufacturing Office (AMMTO) and Bioenergy Technologies Office (BETO). This work was performed as part of the Bio-Optimized Technologies to keep Thermoplastics out of Landfills and the Environment (BOTTLE) Consortium and was supported by AMMTO and BETO at the National Renewable Energy Laboratory for the US Department of Energy (DOE) under Contract No. DE-AC36-08GO28308. The BOTTLE Consortium includes members from Massachusetts Institute of Technology, University of Puerto Rico — Mayagüez, and Colorado State University. D.K. was in part supported by the Director’s Fellowship — Laboratory Directed Research and Development (LDRD) Program at NREL. The views expressed in the article do not necessarily represent the views of the DOE or the US Government. The US Government retains and the publisher, by accepting the article for publication, acknowledges that the US Government retains a non-exclusive, paid-up, irrevocable, worldwide licence to publish or reproduce the published form of this work, or allow others to do so, for US Government purposes. The authors thank S. Mohammed for help with the Gibbs free energy analysis.
Author information
Authors and Affiliations
Contributions
G.T.B. and D.K. conceptualized the review. D.K. was responsible for data curation. G.T.B., D.K., R.E., J.H.M. and A.Z.W. were responsible for formal analysis and visualization. All authors were involved in writing, reviewing, and editing drafts of the manuscript. G.T.B. supervised and administered the project and was responsible for funding acquisition.
Corresponding author
Ethics declarations
Competing interests
Several of the authors have filed patent applications on chemo-catalytic lactone production, but the specific technology is not discussed herein. D.K. and G.T.B. are inventors on a patent application (US patent application no. 63/790,923) that covers lactone production from diols. J.H.M., E.Y.-X.C., and G.T.B. are inventors on a patent application (US patent application no. 63/843,527) that covers β-lactone production. Y.R.-L. is an inventor on a patent application (US patent application no. 19/279,265) that covers a continuous method for producing lactones.
Peer review
Peer review information
Nature Reviews Chemistry thanks Mukund Sibi, George Huber, and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Kiani, D., Eaglesfield, R., May, J.H. et al. Production of bio-based lactones as monomers for a circular polymer economy. Nat Rev Chem 9, 749–765 (2025). https://doi.org/10.1038/s41570-025-00765-9
Accepted:
Published:
Version of record:
Issue date:
DOI: https://doi.org/10.1038/s41570-025-00765-9