TY - JOUR
T1 - The Chemistry of Levulinic Acid
T2 - Its Potential in the Production of Biomass-Based Chemicals
AU - Árvai, Csaba
AU - Medgyesi, Zoltán
AU - Lui, Matthew Y.
AU - Mika, László T.
N1 - Funding Information:
L. T. Mika thanks to the support of the National Research, Development and Innovation Office – NKFIH, project FK 143197. L. T. Mika is grateful for the support of Project No. TKP2021-EGA-02, implemented with the support provided by the Ministry for Innovation and Technology of Hungary from the National Research, Development and Innovation Fund, financed under the TKP2021 funding scheme.
Publisher Copyright:
© 2024 The Author(s). Advanced Synthesis & Catalysis published by Wiley-VCH GmbH.
PY - 2024/12/3
Y1 - 2024/12/3
N2 - Biomass has been identified as the ultimate sustainable resource for all carbon-based consumer products of the chemical industries in the future. Its catalytic conversion leads to the formation of various platform chemicals that could partially or even fully replace the fossil-based building blocks that have been currently used in synthetic chemical processes. Among these compounds, levulinic acid (LA) has been recognized as a member of the “Top Value Added Chemicals from Biomass” and has attracted significant attention since the seminal paper reported by Werpy and Petersen in 2004. This review summarizes the properties, recent advances, and developments in the chemistry of levulinic acid. The production of LA from both plant and animal-based carbohydrate feedstocks via 5-hydroxymethylfurfural or furfuryl alcohol is discussed from a mechanistic perspective, highlighting intrinsic molecular-level limitations to LA formation. The efficiencies of recently developed catalytic systems are also summarized and compared. Furthermore, the conversion of LA into high-value-added downstream chemicals, including its role in the synthesis of complex molecular structures, is overviewed. This section discussed the reactions of LA in the points of view of its various transformations on carbonyl-, carboxy-, methyl-, and methylene functional groups. The reactions of these functionalities with C−, N−, O−, and S-nucleophiles, alcohols, amines, organometallic reagents, oxygen etc. were thematically summarized. Our review also outlooks to highlight the challenges and opportunities associated with the extensive research area of organic chemistry of levulinic acid.
AB - Biomass has been identified as the ultimate sustainable resource for all carbon-based consumer products of the chemical industries in the future. Its catalytic conversion leads to the formation of various platform chemicals that could partially or even fully replace the fossil-based building blocks that have been currently used in synthetic chemical processes. Among these compounds, levulinic acid (LA) has been recognized as a member of the “Top Value Added Chemicals from Biomass” and has attracted significant attention since the seminal paper reported by Werpy and Petersen in 2004. This review summarizes the properties, recent advances, and developments in the chemistry of levulinic acid. The production of LA from both plant and animal-based carbohydrate feedstocks via 5-hydroxymethylfurfural or furfuryl alcohol is discussed from a mechanistic perspective, highlighting intrinsic molecular-level limitations to LA formation. The efficiencies of recently developed catalytic systems are also summarized and compared. Furthermore, the conversion of LA into high-value-added downstream chemicals, including its role in the synthesis of complex molecular structures, is overviewed. This section discussed the reactions of LA in the points of view of its various transformations on carbonyl-, carboxy-, methyl-, and methylene functional groups. The reactions of these functionalities with C−, N−, O−, and S-nucleophiles, alcohols, amines, organometallic reagents, oxygen etc. were thematically summarized. Our review also outlooks to highlight the challenges and opportunities associated with the extensive research area of organic chemistry of levulinic acid.
KW - Biomass conversion
KW - Levulinic acid
KW - Nucleophile addition
KW - Oxidation
KW - Platform chemicals
KW - Reaction mechanism
KW - Valorization
UR - http://www.scopus.com/inward/record.url?scp=85210028498&partnerID=8YFLogxK
U2 - 10.1002/adsc.202401086
DO - 10.1002/adsc.202401086
M3 - Review article
AN - SCOPUS:85210028498
SN - 1615-4150
VL - 366
SP - 4846
EP - 4888
JO - Advanced Synthesis and Catalysis
JF - Advanced Synthesis and Catalysis
IS - 23
ER -