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Scalable Lipase-Catalyzed Synthesis of (R)-4-(Acyloxy)pentanoic Acids from Racemic γ-Valerolactone

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/chir.22217openalex-snapshot
Synthesis and Quantitative Analysis of Diastereomeric Linked Ester Conjugates With Remote Stereocenters Using High‐Field NMR and Chiral HPLC
inferredcites →https://doi.org/10.1002/cssc.201301397openalex-snapshot
Catalytic Conversion of γ‐Valerolactone to ε‐Caprolactam: Towards Nylon from Renewable Feedstock
inferredcites →https://doi.org/10.1002/cssc.201801620openalex-snapshot
Catalytic Transfer Hydrogenation of Biomass‐Derived Substrates to Value‐Added Chemicals on Dual‐Function Catalysts: Opportunities and Challenges
inferredcites →https://doi.org/10.1002/marc.201100230openalex-snapshot
Cellulose‐Based Sustainable Polymers: State of the Art and Future Trends
inferredcites →https://doi.org/10.1007/s00253-012-4652-5openalex-snapshot
A chemo-enzymatic route to synthesize (S)-γ-valerolactone from levulinic acid
inferredcites →https://doi.org/10.1007/s10562-017-2291-2openalex-snapshot
Facile Synthesis of Optically-Active γ-Valerolactone from Levulinic Acid and Its Esters Using a Heterogeneous Enantio-Selective Catalyst
inferredcites →https://doi.org/10.1007/s11172-006-0125-2openalex-snapshot
Enantioselective hydrogenation of levulinic acid esters in the presence of the RuII-BINAP-HCl catalytic system
inferredcites →https://doi.org/10.1016/0040-4020(75)80138-4openalex-snapshot
Synthesis of optically active forms of sulcatol
inferredcites →https://doi.org/10.1016/j.tetasy.2016.05.008openalex-snapshot
Stereoselective synthesis of (R)-(−) and (S)-(+)-phoracantholide I from (R)-(+)-γ-valerolactone
inferredcites →https://doi.org/10.1016/j.theochem.2007.10.045openalex-snapshot
A total conformational analysis of diastereomeric esters and calculation of their conformational shielding models
inferredcites →https://doi.org/10.1016/s0021-9673(00)00375-7openalex-snapshot
Insoluble β-cyclodextrin polymer for capillary gas chromatographic separation of enantiomers and isomers
inferredcites →https://doi.org/10.1016/s0040-4039(02)00418-5openalex-snapshot
Dynamic kinetic resolution of γ-hydroxy acid derivatives
inferredcites →https://doi.org/10.1016/s0168-1656(97)00107-7openalex-snapshot
Lipase-catalysed resolution of γ- and δ-lactones
inferredcites →https://doi.org/10.1016/s0921-3449(99)00047-6openalex-snapshot
Production of levulinic acid and use as a platform chemical for derived products
inferredcites →https://doi.org/10.1016/s0957-4166(98)00053-6openalex-snapshot
The tetrahydropyranyl-protected mandelic acid: a novel versatile chiral derivatising agent
inferredcites →https://doi.org/10.1021/acscatal.7b02183openalex-snapshot
Combination of Metal-Catalyzed Cycloisomerizations and Biocatalysis in Aqueous Media: Asymmetric Construction of Chiral Alcohols, Lactones, and γ-Hydroxy-Carbonyl Compounds
inferredcites →https://doi.org/10.1021/acsomega.9b03424openalex-snapshot
Room-Temperature Asymmetric Transfer Hydrogenation of Biomass-Derived Levulinic Acid to Optically Pure γ-Valerolactone Using a Ruthenium Catalyst
inferredcites →https://doi.org/10.1021/acssuschemeng.8b05074openalex-snapshot
Enzymatic Synthesis and Polymerization of Isosorbide-Based Monomethacrylates for High-Tg Plastics
inferredcites →https://doi.org/10.1021/cr000665jopenalex-snapshot
The Assignment of Absolute Configuration by NMR
inferredcites →https://doi.org/10.1021/cs4010024openalex-snapshot
Stereodivergent Preparation of Valuable γ- or δ-Hydroxy Esters and Lactones through One-Pot Cascade or Tandem Chemoenzymatic Protocols
inferredcites →https://doi.org/10.1021/cs501922eopenalex-snapshot
Environmentally Friendly Synthesis of γ-Valerolactone by Direct Catalytic Conversion of Renewable Sources
inferredcites →https://doi.org/10.1021/ja00389a064openalex-snapshot
Quantitative analyses of biochemical kinetic resolutions of enantiomers
inferredcites →https://doi.org/10.1021/ja049463lopenalex-snapshot
Sequential Arrangement of γ-Valerolactone Enantiomers Enclathrated in Cholic Acid Channels as Studied by 13C Solid-State NMR: Elucidation of the Optical Resolution Mechanism
inferredcites →https://doi.org/10.1021/ja071241aopenalex-snapshot
Switching from S- to R-Selectivity in the Candida antarctica Lipase B-Catalyzed Ring-Opening of ω-Methylated Lactones: Tuning Polymerizations by Ring Size
inferredcites →https://doi.org/10.1021/jo00265a003openalex-snapshot
Total synthesis of geodiamolide A, a novel cyclodepsipeptide of marine origin
inferredcites →https://doi.org/10.1021/jo00293a044openalex-snapshot
Efficient oxidation of phenyl groups to carboxylic acids with ruthenium tetraoxide. A simple synthesis of (R)-.gamma.-caprolactone, the pheromone of Trogoderma granarium
inferredcites →https://doi.org/10.1021/jo0478252openalex-snapshot
Kinetic Resolution and Chemoenzymatic Dynamic Kinetic Resolution of Functionalized γ-Hydroxy Amides
inferredcites →https://doi.org/10.1039/b409061fopenalex-snapshot
A convenient route to optically active γ-substituted γ-lactones
inferredcites →https://doi.org/10.1039/b712863kopenalex-snapshot
γ-Valerolactone—a sustainable liquid for energy and carbon-based chemicals
inferredcites →https://doi.org/10.1039/c1an15205jopenalex-snapshot
4,6-Di-O-pentyl-3-O-trifluoroacetyl/propionyl cyclofructan stationary phases for gas chromatographic enantiomeric separations
inferredcites →https://doi.org/10.1039/c3gc37065hopenalex-snapshot
Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
inferredcites →https://doi.org/10.1039/c5gc00340gopenalex-snapshot
Towards a holistic approach to metrics for the 21st century pharmaceutical industry
inferredcites →https://doi.org/10.1039/c5gc01099copenalex-snapshot
Direct asymmetric reduction of levulinic acid to gamma-valerolactone: synthesis of a chiral platform molecule
inferredcites →https://doi.org/10.1039/c8gc02001aopenalex-snapshot
Valorization of levulinic acid over non-noble metal catalysts: challenges and opportunities
inferredcites →https://doi.org/10.1039/p19900002469openalex-snapshot
Baker's yeast-mediated preparation of optically active aryl alcohols and diols for the synthesis of chiral hydroxy acids
inferredcites →https://doi.org/10.1080/00397919008052803openalex-snapshot
Bakers' Yeast Reductions of Alkyl Levulinates: Synthesis of (R)-(+) and (S)-(-)4-methylbutyrolactones

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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High Entropy Alloys Loaded Hollow Nanoreactors For Conversion of Acetylpropionic Acid to Γ-Valerolactone
inferred← citeshttps://doi.org/10.1002/bbb.2394openalex-snapshot
Effective one‐pot tandem synthesis of γ‐valerolactone from biogenic furfural over zirconium phosphate catalyst
inferred← citeshttps://doi.org/10.1002/ejoc.202201329openalex-snapshot
Stereoselective Synthesis of γ‐(Acyloxy)carboxylic Acids and γ‐Lactones Featuring the Switch of Stereopreference of Candida antarctica Lipase B in Sodium γ‐Hydroxycarboxylate Homologues
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inferred← citeshttps://doi.org/10.1016/j.matpr.2021.05.020openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c07430openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d5qo00520eopenalex-snapshot
Access to ester-substituted γ-butyrolactones via photocatalyzed alkoxycarbonylation/lactonization of alkenoic acids
inferred← citeshttps://doi.org/10.1063/5.0240619openalex-snapshot
Impact of nano biomaterials as PPE coatings to prevent COVID-19: A review article
inferred← citeshttps://doi.org/10.3762/bjoc.21.165openalex-snapshot
C2 to C6 biobased carbonyl platforms for fine chemistry
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