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Synthetic approaches towards structurally diverse γ-butyrolactone natural-product-like compounds
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1099-0690(200008)2000:16<2955::aid-ejoc2955>3.0.co;2-3openalex-snapshot
A New Strategy for the Stereoselective Synthesis of 1,2,3-Trisubstituted Cyclopropanes
inferredcites →https://doi.org/10.1002/1521-3773(20010119)40:2<339::aid-anie339>3.0.co;2-jopenalex-snapshot
Diversity-Based Organic Synthesis in the Era of Genomics and Proteomics
inferredcites →https://doi.org/10.1002/1521-3773(20020503)41:9<1584::aid-anie1584>3.0.co;2-yopenalex-snapshot
Synthesis ofα-Methylene-γ-butyrolactones: Ru-Catalyzed Cyclocarbonylation of Allenyl Aldehydes and Allenyl Ketones
inferredcites →https://doi.org/10.1002/anie.198500941openalex-snapshot
Synthesis and Biological Activity of α‐Methylene‐γ‐butyrolactones
inferredcites →https://doi.org/10.1002/anie.199722821openalex-snapshot
Enantioselective Synthesis with Lithium/(−)‐Sparteine Carbanion Pairs
inferredcites →https://doi.org/10.1002/anie.199727501openalex-snapshot
Synthesis of Optically Active Butenolides and γ‐Lactones by the Sharpless Asymmetric Dihydroxylation of β,γ‐Unsaturated Carboxylic Esters
inferredcites →https://doi.org/10.1002/anie.200461572openalex-snapshot
Organocatalyzed Conjugate Umpolung of α,β‐Unsaturated Aldehydes for the Synthesis of γ‐Butyrolactones
inferredcites →https://doi.org/10.1002/chem.200305634openalex-snapshot
A “Chiral Aldehyde” Equivalent as a Building Block Towards Biologically Active Targets
inferredcites →https://doi.org/10.1002/chem.200390019openalex-snapshot
Enantioselective Synthesis of Paraconic Acids
inferredcites →https://doi.org/10.1002/chem.200400237openalex-snapshot
Stereoselective Synthesis of (+)‐Nephrosteranic Acid, (+)‐trans‐Cognac Lactone, and (+)‐trans‐Whisky Lactone using a Chiral Cyclohexadienyl Ti Compound
inferredcites →https://doi.org/10.1002/chin.200507091openalex-snapshot
Stereoselective Synthesis of Highly Substituted Bicyclic γ‐Lactones Using Homoaldol Addition of 1‐(1‐Cycloalkenyl)methyl Carbamates.
inferredcites →https://doi.org/10.1007/b96881openalex-snapshot
Paraconic Acids—The Natural Products from Lichen Symbiont
inferredcites →https://doi.org/10.1016/b978-0-444-89366-6.70001-0openalex-snapshot
Studies in Natural Products Chemistry
inferredcites →https://doi.org/10.1016/s0040-4020(97)00199-3openalex-snapshot
Regio- and stereoselective synthesis of γ-alkylidenebutenolides and related compounds
inferredcites →https://doi.org/10.1016/s1074-5521(02)00105-9openalex-snapshot
Toward High-Throughput Synthesis of Complex Natural Product-Like Compounds in the Genomics and Proteomics Age
inferredcites →https://doi.org/10.1016/s1367-5931(02)00338-1openalex-snapshot
Modern methods to produce natural-product libraries
inferredcites →https://doi.org/10.1016/s1572-5995(06)80065-7openalex-snapshot
Enantiomerically pure γ-butyrolactones in natural products synthesis
inferredcites →https://doi.org/10.1021/cc0001001openalex-snapshot
Solution- and Solid-Phase Strategies for the Design, Synthesis, and Screening of Libraries Based on Natural Product Templates: A Comprehensive Survey
inferredcites →https://doi.org/10.1021/cr0200217openalex-snapshot
Catalytic Enantioselective C−H Activation by Means of Metal−Carbenoid-Induced C−H Insertion
inferredcites →https://doi.org/10.1021/ja001379sopenalex-snapshot
Highly Enantioselective Palladium(II)-Catalyzed Cyclization of (Z)-4‘-Acetoxy-2‘-butenyl 2-Alkynoates: An Efficient Synthesis of Optically Active γ-Butyrolactones
inferredcites →https://doi.org/10.1021/ja005568mopenalex-snapshot
γ-Butyrolactone Synthesis via Catalytic Asymmetric Cyclocarbonylation
inferredcites →https://doi.org/10.1021/ja017545topenalex-snapshot
Nickel-BINAP Catalyzed Enantioselective α-Arylation of α-Substituted γ-Butyrolactones
inferredcites →https://doi.org/10.1021/ja029095qopenalex-snapshot
The First Enantioselective Organocatalytic Mukaiyama−Michael Reaction: A Direct Method for the Synthesis of Enantioenriched γ-Butenolide Architecture
inferredcites →https://doi.org/10.1021/ja044714bopenalex-snapshot
N-Heterocyclic Carbene-Catalyzed Generation of Homoenolates: γ-Butyrolactones by Direct Annulations of Enals and Aldehydes
inferredcites →https://doi.org/10.1021/ja962965hopenalex-snapshot
A Facile Synthesis of Chiral γ-Butyrolactones in Extremely High Enantioselectivity Mediated by Samarium(II) Iodide
inferredcites →https://doi.org/10.1021/ja970115bopenalex-snapshot
Titanocene-Catalyzed Cyclocarbonylation of o-Allyl Aryl Ketones to γ-Butyrolactones
inferredcites →https://doi.org/10.1021/ja991223wopenalex-snapshot
Ruthenium Carbonyl-Catalyzed [2 + 2 + 1]- Cycloaddition of Ketones, Olefins, and Carbon Monoxide, Leading to Functionalized γ-Butyrolactones
inferredcites →https://doi.org/10.1021/ja992013mopenalex-snapshot
Ruthenium-Catalyzed Cycloisomerization−Oxidation of Homopropargyl Alcohols. A New Access to γ-Butyrolactones
inferredcites →https://doi.org/10.1021/ja992144nopenalex-snapshot
Synthesis and Preliminary Evaluation of a Library of Polycyclic Small Molecules for Use in Chemical Genetic Assays
inferredcites →https://doi.org/10.1021/jo0002487openalex-snapshot
Total Synthesis of (+)-Blastmycinone, (−)-Litsenolide C1, and Related Natural Trisubstituted Lactones via Alkynyltungsten Compounds
inferredcites →https://doi.org/10.1021/jo00271a050openalex-snapshot
Synthesis of enantiomerically pure .gamma.-(menthyloxy)butenolides and (R)- and (S)-2-methyl-1,4-butanediol
inferredcites →https://doi.org/10.1021/jo020574hopenalex-snapshot
One-Step Highly Diastereoselective Synthesis of γ-Aminoalkyl-Substituted γ-Butyrolactones by an Asymmetric Samarium-Mediated Ketyl−Alkene Coupling Reaction
inferredcites →https://doi.org/10.1021/jo049027hopenalex-snapshot
Highly Stereoselective Aldol Reaction for the Synthesis of γ-Lactones Starting from Tartaric Acid
inferredcites →https://doi.org/10.1021/jo961171iopenalex-snapshot
Enantiospecific Synthesis of Trisubstituted Butyrolactone Natural Products and Their Analogs
inferredcites →https://doi.org/10.1021/jo961607uopenalex-snapshot
Intramolecular Regioselective Insertion into Unactivated Prochiral Carbon−Hydrogen Bonds with Diazoacetates of Primary Alcohols Catalyzed by Chiral Dirhodium(II) Carboxamidates. Highly Enantioselective Total Synthesis of Natural Lignan Lactones
inferredcites →https://doi.org/10.1021/jo991211topenalex-snapshot
Enantioselective Syntheses of 2-Deoxyxylono-1,4-lactone and 2-Deoxyribono-1,4-lactone from 1,3-Dioxan-5-yl Diazoacetates
inferredcites →https://doi.org/10.1021/jo991692gopenalex-snapshot
Palladium-Catalyzed Heteroannulation of 1,3-Dienes To Form α-Alkylidene-γ-butyrolactones
inferredcites →https://doi.org/10.1021/ol0069960openalex-snapshot
Stereoselective Synthesis of Substituted γ-Butyrolactones by the [3 + 2] Annulation of Allylic Silanes with Chlorosulfonyl Isocyanate: Enantioselective Total Synthesis of (+)-Blastmycinone
inferredcites →https://doi.org/10.1021/ol015686uopenalex-snapshot
Enantioselective Synthesis of (−)-Roccellaric Acid
inferredcites →https://doi.org/10.1021/ol026489dopenalex-snapshot
A General Method for the Enantioselective Synthesis of Pantolactone Derivatives
inferredcites →https://doi.org/10.1021/ol034141sopenalex-snapshot
Facile Asymmetric Synthesis of the Core Nuclei of Xanthanolides, Guaianolides, and Eudesmanolides
inferredcites →https://doi.org/10.1021/ol047821jopenalex-snapshot
Complementary Diastereoselective Reduction of Cyclic γ-Keto Acids: Efficient Access to Trisubsituted γ-Lactones
inferredcites →https://doi.org/10.1055/s-2004-831170openalex-snapshot
Stereoselective Synthesis of Highly Substituted Bicyclic γ-Lactones Using Homoaldol Addition of 1-(1-Cycloalkenyl)methyl Carbamates
inferredcites →https://doi.org/10.1055/s-2005-864827openalex-snapshot
Radical Cyclizations as Key Step for the Stereoselective Synthesis of Bi- and Tricyclic Sesquiterpene Lactones
inferredcites →https://doi.org/10.2174/138620703771981232openalex-snapshot
Natural Product-Like and Other Biologically Active Heterocyclic Libraries Using Solid-Phase Techniques in the Post-Genomic Era
inferredcites →https://doi.org/10.3892/or.8.1.173openalex-snapshot
Arglabin-DMA, a plant derived sesquiterpene, inhibits farnesyltransferase.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Inverse Electron Demand Diels-Alder Reaction in Total Synthesis of Bioactive Natural Products
inferred← citeshttps://doi.org/10.1002/adsc.201300859openalex-snapshot
Flow Synthesis of Substituted γ‐Lactones by Consecutive Photocatalytic/Reductive Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201400041openalex-snapshot
De Novo Synthesis of γ,γ‐Disubstituted Butyrolactones through a Visible Light Photocatalytic Arylation–Lactonization Sequence
inferred← citeshttps://doi.org/10.1002/adsc.201901483openalex-snapshot
Biocatalytic Asymmetric Reduction of γ‐Keto Esters to Access Optically Active γ‐Aryl‐γ‐butyrolactones
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Remote Functionalization of 4‐(Alk‐1‐en‐1‐yl)‐3‐Cyanocoumarins via the Asymmetric Organocatalytic 1,6‐Addition
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Synergistic Copper‐Aminocatalysis for Direct Tertiary α‐Alkylation of Ketones with Electron‐Deficient Alkanes
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Recent Advances in Total Synthesis of Bioactive Furo[3,2‐b]furanone Natural Products
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Evolution of Strategies in Paraconic Acids Synthesis
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Gold‐Catalyzed Carboxylative Cyclization Reactions: Recent Advances
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Diastereoselective Synthesis of Pentasubstituted γ‐Butyrolactones from Silyl Glyoxylates and Ketones through a Double Reformatsky Reaction
inferred← citeshttps://doi.org/10.1002/ange.201102404openalex-snapshot
Modular Monodentate Oxaphospholane Ligands: Utility in Highly Efficient and Enantioselective 1,4‐Diboration of 1,3‐Dienes
inferred← citeshttps://doi.org/10.1002/ange.201203637openalex-snapshot
Gold‐katalysierte Synthese von Furanen und Furanonen aus Schwefel‐Yliden
inferred← citeshttps://doi.org/10.1002/ange.201609960openalex-snapshot
Iridium‐Catalyzed Stereoselective Allylic Alkylation Reactions with Crotyl Chloride
inferred← citeshttps://doi.org/10.1002/ange.201912618openalex-snapshot
Copper‐Catalyzed Enantioselective Allylic Alkylation with a γ‐Butyrolactone‐Derived Silyl Ketene Acetal
inferred← citeshttps://doi.org/10.1002/ange.202107418openalex-snapshot
Stereodivergent Synthesis of Enantioenriched γ‐Butyrolactones Bearing Two Vicinal Stereocenters Enabled by Synergistic Copper and Iridium Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202209004openalex-snapshot
Asymmetric Oxidative Lactonization of Enynyl Boronates
inferred← citeshttps://doi.org/10.1002/ange.202300537openalex-snapshot
Organocatalytic Synthesis of Triflones Bearing Two Non‐Adjacent Stereogenic Centers
inferred← citeshttps://doi.org/10.1002/ange.202304275openalex-snapshot
Copper‐Catalyzed Radical Enantioselective Synthesis of γ‐Butyrolactones with Two Non‐vicinal Carbon Stereocenters
inferred← citeshttps://doi.org/10.1002/ange.202308636openalex-snapshot
Electrochemical Gold‐Catalyzed 1,2‐Difunctionalization of C−C Multiple Bonds**
inferred← citeshttps://doi.org/10.1002/ange.202412828openalex-snapshot
Cobalt‐Catalyzed Intramolecular Markovnikov Hydrocarbonylation of Unactivated Alkenes via Hydrogen Atom Transfer
inferred← citeshttps://doi.org/10.1002/anie.200900215openalex-snapshot
Diastereoselective Synthesis of Pentasubstituted γ‐Butyrolactones from Silyl Glyoxylates and Ketones through a Double Reformatsky Reaction
inferred← citeshttps://doi.org/10.1002/anie.201102404openalex-snapshot
Modular Monodentate Oxaphospholane Ligands: Utility in Highly Efficient and Enantioselective 1,4‐Diboration of 1,3‐Dienes
inferred← citeshttps://doi.org/10.1002/anie.201203637openalex-snapshot
Gold‐Catalyzed Synthesis of Furans and Furanones from Sulfur Ylides
inferred← citeshttps://doi.org/10.1002/anie.201609960openalex-snapshot
Iridium‐Catalyzed Stereoselective Allylic Alkylation Reactions with Crotyl Chloride
inferred← citeshttps://doi.org/10.1002/anie.201912618openalex-snapshot
Copper‐Catalyzed Enantioselective Allylic Alkylation with a γ‐Butyrolactone‐Derived Silyl Ketene Acetal
inferred← citeshttps://doi.org/10.1002/anie.202107418openalex-snapshot
Stereodivergent Synthesis of Enantioenriched γ‐Butyrolactones Bearing Two Vicinal Stereocenters Enabled by Synergistic Copper and Iridium Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202209004openalex-snapshot
Asymmetric Oxidative Lactonization of Enynyl Boronates
inferred← citeshttps://doi.org/10.1002/anie.202300537openalex-snapshot
Organocatalytic Synthesis of Triflones Bearing Two Non‐Adjacent Stereogenic Centers
inferred← citeshttps://doi.org/10.1002/anie.202304275openalex-snapshot
Copper‐Catalyzed Radical Enantioselective Synthesis of γ‐Butyrolactones with Two Non‐vicinal Carbon Stereocenters
inferred← citeshttps://doi.org/10.1002/anie.202308636openalex-snapshot
Electrochemical Gold‐Catalyzed 1,2‐Difunctionalization of C−C Multiple Bonds**
inferred← citeshttps://doi.org/10.1002/anie.202412828openalex-snapshot
Cobalt‐Catalyzed Intramolecular Markovnikov Hydrocarbonylation of Unactivated Alkenes via Hydrogen Atom Transfer
inferred← citeshttps://doi.org/10.1002/cctc.201402967openalex-snapshot
Iron(II) Pincer‐Catalyzed Synthesis of Lactones and Lactams through a Versatile Dehydrogenative Domino Sequence
inferred← citeshttps://doi.org/10.1002/cctc.201801040openalex-snapshot
Enantioselective, Catalytic One‐Pot Synthesis of γ‐Butyrolactone‐Based Fragrances
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Efficient Stereoselective Synthesis of Structurally Diverse γ‐ and δ‐Lactones Using an Engineered Carbonyl Reductase
inferred← citeshttps://doi.org/10.1002/cctc.202200855openalex-snapshot
The Synthesis of Chiral γ‐Lactones by Merging Decatungstate Photocatalysis with Biocatalysis
inferred← citeshttps://doi.org/10.1002/cctc.202500060openalex-snapshot
Organo‐, Metal‐, and Enzyme‐Mediated Stereoselective Transformations of α‐Angelica Lactone
inferred← citeshttps://doi.org/10.1002/chem.200802178openalex-snapshot
Convenient Synthesis of Bicyclic Carbohydrate 1,2‐Lactones and Their Stereoselective Opening to 1‐Functionalized Glucose Derivatives
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Catalytic, Asymmetric Synthesis of Phosphonic γ‐(Hydroxyalkyl)butenolides with Contiguous Quaternary and Tertiary Stereogenic Centers
inferred← citeshttps://doi.org/10.1002/chem.201404607openalex-snapshot
Carbon‐Centered Radical Addition to OC of Amides or Esters as a Route to CO Bond Formations
inferred← citeshttps://doi.org/10.1002/chem.201500861openalex-snapshot
Asymmetric Copper‐Catalyzed Vinylogous Mukaiyama Michael Addition of Cyclic Dienol Silanes to Unsaturated α‐Keto Phosphonates
inferred← citeshttps://doi.org/10.1002/chem.201501106openalex-snapshot
Rhodium(III)‐Catalyzed [4+1] Annulation of Aromatic and Vinylic Carboxylic Acids with Allenes: An Efficient Method Towards Vinyl‐Substituted Phthalides and 2‐Furanones
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Synthesis of α‐Chiral Butyrolactones by Highly Stereoselective Radical Transfer or Sequential Asymmetric Alkylations: Concise Preparation of Leupyrrin Moieties
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Synergistic Diazo‐OH Insertion/Conia‐Ene Cascade Catalysis for the Stereoselective Synthesis of γ‐Butyrolactones and Tetrahydrofurans
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Synthesis of γ,γ‐Disubstituted Butenolides through a Doubly Vinylogous Organocatalytic Cycloaddition
inferred← citeshttps://doi.org/10.1002/chem.202000747openalex-snapshot
A Sequential Umpolung/Enzymatic Dynamic Kinetic Resolution Strategy for the Synthesis of γ‐Lactones
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Peptide Catalyzed Conjugate Additions to β‐Nitroacrylates – Steric Bulk Increases the Reaction Rate
inferred← citeshttps://doi.org/10.1002/chin.200613263openalex-snapshot
Synthetic Approaches Towards Structurally Diverse γ‐Butyrolactone Natural Product‐Like Compounds
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Absolute Configuration Assignment of a Paraconic Acid Derivative via Vibrational Circular Dichroism Spectroscopy and Density Functional Theory Calculation
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Estimation of optical rotation of γ‐alkylidenebutenolide, cyclopropylamine, cyclopropyl‐methanol and cyclopropenone based compounds by a Density Functional Theory (DFT) approach
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An Efficient Enantioselective Synthesis of Blastmycinone
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Catalytic Enantioselective Simultaneous Control of Axial Chirality and Central Chirality in Allenes
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Visible‐Light‐Driven Metal‐Free C−H Functionalization: Access to New Bioactive Tetrahydroisoquinoline‐Butenolide Hybrids via Domino Amine Oxidation/Vinylogous Mannich Reaction**
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Angelica Lactones: From Biomass‐Derived Platform Chemicals to Value‐Added Products
inferred← citeshttps://doi.org/10.1002/cssc.202402224openalex-snapshot
Electrosynthesis of γ‐Butyrolactones by Dehydrogenative (3+2) Annulation
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Synthesis of Biologically Active Guaianolides with a trans ‐Annulated Lactone Moiety
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Syntheses of a Flobufen Metabolite and Dapoxetine Based on Enantioselective Allylation of Aromatic Aldehydes
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Total Synthesis and Structural Reassignment of the γ‐Lactone Polyketide from Diaporthe sp. SXZ‐19
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Nonracemic γ‐Lactones from the Sharpless Asymmetric Dihydroxylation of β,γ‐Unsaturated Carboxylic Esters
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A Passerini/Michael Pathway towards Butyrolactones
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Flow Chemistry: Towards A More Sustainable Heterocyclic Synthesis
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AlCl 3 ‐Promoted Ritter‐Type Ring‐Opening Reactions of γ‐Butyrolactone Fused Donor‐Acceptor Cyclopropanes with Wet Aliphatic Nitriles
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Regio‐ and Enantioselective Substrate‐Directed Epoxidation
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Metal‐Free Arylation‐Lactonization Sequence of γ‐Alkenoic Acids Using Anilines as Aryl Radical Precursors
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Diastereoselective Synthesis of γ‐Lactones through Reaction of Sulfoxonium Ylides, Aldehydes, and Ketenes: Substrate Scope and Mechanistic Studies
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Tandem Friedel‐Crafts Alkylation/Lactonization for γ‐Lactone
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Acid‐Promoted Structural Reorganization of Pull–Pull Alkylidenecyclobutanes: A Cascade Synthesis of Three‐Substituted γ‐Butyrolactones
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Synthesis of Perfluoroalkyl‐Substitutedγ‐Lactones and 4,5‐Dihydropyridazin‐3(2H)‐onesviaDonorAcceptor Cyclopropanes
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Catalytic Conversion of Furans and Pyrroles to Natural Products and Analogues Utilizing Donor‐Acceptor Substituted Cyclopropanes as Key Intermediates
inferred← citeshttps://doi.org/10.1002/jhet.2266openalex-snapshot
Synthesis of Novel Dibenzylbutyrolactones as Dimethylmatairesinol Analogues
inferred← citeshttps://doi.org/10.1002/mrc.1965openalex-snapshot
Determination of the stereochemistry of γ‐Butyrolactones by DPFGSE‐NOE experiments
inferred← citeshttps://doi.org/10.1002/open.202000220openalex-snapshot
Protonation of γ‐Butyrolactone and γ‐Butyrolactam
inferred← citeshttps://doi.org/10.1002/slct.201700339openalex-snapshot
Synthesis of Alkynylated Dihydrofuran‐2(3 H )‐ones as Potent and Selective Inhibitors of Tissue Non‐Specific Alkaline Phosphatase
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Organocatalytic Asymmetric Cascade Reaction of γ‐Substituted Deconjugated Butenolides with o‐Formyl‐β‐nitrostyrene
inferred← citeshttps://doi.org/10.1002/slct.202405837openalex-snapshot
Photocatalyzed Carbon─Carbon Bond Formation Between Ethylene Glycol and Electron‐Deficient Olefins
inferred← citeshttps://doi.org/10.1002/tcr.201600022openalex-snapshot
Asymmetric Aldol Reaction with Formaldehyde: a Challenging Process
inferred← citeshttps://doi.org/10.1002/tcr.201800095openalex-snapshot
Carbon‐Carbon and Carbon‐Heteroatom Bond Formation Reactions Using Unsaturated Carbon Compounds
inferred← citeshttps://doi.org/10.1007/2789_2008_081openalex-snapshot
Nucleophilic Carbenes as Organocatalysts
inferred← citeshttps://doi.org/10.1007/978-3-030-11155-7_26-1openalex-snapshot
Synthesis of Heterocycles Over Nanoporous Zeolites
inferred← citeshttps://doi.org/10.1007/978-981-13-8499-8_15openalex-snapshot
Active Compounds and Bacteria Harbouring Capacity of Lichens and Its Medicinal Use in Bacterial and Cancer Infections
inferred← citeshttps://doi.org/10.1007/s00253-006-0611-3openalex-snapshot
Ecological and biotechnological aspects of lichens
inferred← citeshttps://doi.org/10.1007/s10593-018-2290-2openalex-snapshot
Intramolecular [4+2] cycloaddition in N-allyl- and N-propargyl-α-furyl lactams
inferred← citeshttps://doi.org/10.1007/s11164-016-2476-0openalex-snapshot
Preparation of 3,4,5-substituted furan-2(5H)-ones using HY Zeolite nano-powder as an efficient catalyst
inferred← citeshttps://doi.org/10.1007/s11164-018-3406-0openalex-snapshot
Synthesis of 3,4,5-substituted furan-2(5H)-ones using Al-doped ZnO nanostructure
inferred← citeshttps://doi.org/10.1007/s11696-016-0013-7openalex-snapshot
Synthesis of tricyclic ring systems: [2+2] ketene addition reaction for preparation of tricyclic ketone, alcohol, and lactone derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-12-800070-0.00010-4openalex-snapshot
Green and Catalytic Methods for γ-Lactone Synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-12-820792-5.00002-0openalex-snapshot
Green and catalytic methods for γ-lactone synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-12-824285-8.00001-7openalex-snapshot
Applications of 2-Oxoacids
inferred← citeshttps://doi.org/10.1016/b978-0-323-91095-8.00009-xopenalex-snapshot
Asymmetric synthesis of butyrolactones by aldol reactions
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00055-7openalex-snapshot
The Aldol Reaction: Group I and II enolates
inferred← citeshttps://doi.org/10.1016/b978-0-443-19057-5.00013-3openalex-snapshot
Biocatalysis for the selective reduction of carbonyl groups
inferred← citeshttps://doi.org/10.1016/j.bmcl.2008.07.095openalex-snapshot
Synthesis and cytotoxic activity of some novel polycyclic γ-butyrolactones
inferred← citeshttps://doi.org/10.1016/j.bmcl.2014.06.045openalex-snapshot
Design and synthesis of γ-butyrolactone derivatives as potential spermicidal agents
inferred← citeshttps://doi.org/10.1016/j.cclet.2009.04.029openalex-snapshot
First synthesis of (±)-cedarmycin B
inferred← citeshttps://doi.org/10.1016/j.chempr.2024.01.003openalex-snapshot
A modular approach to stereoselective homoaldol reaction via photoredox/Cr/Co triple catalysis
inferred← citeshttps://doi.org/10.1016/j.comptc.2021.113534openalex-snapshot
Theoretical conformations studies on 2-Acetyl-gamma-butyrolactone structure and stability in aqueous phase and the solvation effects on electronic properties by quantum computational methods
inferred← citeshttps://doi.org/10.1016/j.crci.2011.03.006openalex-snapshot
Approche synthétique efficace pour l’assemblage d’α-méthylène-γ-butyrolactones diversement fonctionnalisées
inferred← citeshttps://doi.org/10.1016/j.ejmech.2010.09.064openalex-snapshot
Isochaihulactone analogues: Synthesis and anti-proliferative activity of novel dibenzylbutyrolactones
inferred← citeshttps://doi.org/10.1016/j.fmre.2022.07.008openalex-snapshot
Stereodivergent synthesis of α-fluoro α-azaaryl γ-butyrolactones via cooperative copper and iridium catalysis
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2012.03.014openalex-snapshot
Dual reactivity of O-α-allenyl esters under palladium(0) catalysis: From carbopalladation/allylic alkylation domino sequence to decarboxylative allenylation
inferred← citeshttps://doi.org/10.1016/j.jscs.2023.101658openalex-snapshot
Recent advances on copper-catalyzed asymmetric synthesis and their potential biological applications
inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114421openalex-snapshot
Toward an environmentally friendly synthesis of chiral γ-lactones: A biocatalytically oxidative desymmetrization pathway
inferred← citeshttps://doi.org/10.1016/j.molcata.2014.08.032openalex-snapshot
Hydrogenation of succinic acid to γ-butyrolactone and 1,4-butanediol over mesoporous rhenium–copper–carbon composite catalyst
inferred← citeshttps://doi.org/10.1016/j.molstruc.2018.07.091openalex-snapshot
An introduction to the kinetics of the triethylamine-mediated selenocyclofunctionalization of 4-pentenoic acid
inferred← citeshttps://doi.org/10.1016/j.molstruc.2018.10.064openalex-snapshot
Stereochemical assignment of four diastereoisomers of a maculalactone derivative by computational NMR calculations
inferred← citeshttps://doi.org/10.1016/j.scib.2017.01.016openalex-snapshot
Ring strain strategy for the control of regioselectivity. Gold-catalyzed anti-Markovnikov cycloisomerization initiated tandem reactions of alkynes
inferred← citeshttps://doi.org/10.1016/j.tchem.2024.100066openalex-snapshot
Inverse electron demand Diels-Alder reaction in total synthesis of bioactive natural products
inferred← citeshttps://doi.org/10.1016/j.tet.2011.01.069openalex-snapshot
Stereoselective diversity-oriented syntheses of functionalized saccharides from bicyclic carbohydrate 1,2-lactones
inferred← citeshttps://doi.org/10.1016/j.tet.2014.01.057openalex-snapshot
Synthesis of γ-butenolides and α,β-unsaturated γ-butyrolactams by addition of vinylogous nucleophiles to Michael acceptors
inferred← citeshttps://doi.org/10.1016/j.tet.2014.07.039openalex-snapshot
Direct lactonization of α-amino γ,δ-unsaturated carboxylic acid esters via olefin activation: stereo- and regioselective production of homoserine lactone scaffolds having contiguous stereocenters
inferred← citeshttps://doi.org/10.1016/j.tet.2015.07.010openalex-snapshot
Synthesis of α-ketols by functionalization of captodative alkenes and divergent preparation of heterocycles and natural products
inferred← citeshttps://doi.org/10.1016/j.tet.2015.12.071openalex-snapshot
Baeyer–Villiger monooxygenase-catalyzed desymmetrizations of cyclobutanones. Application to the synthesis of valuable spirolactones
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132191openalex-snapshot
β,γ-trans-selective γ-butyrolactone formation via homoenolate cross-annulation of enals and aldehydes catalyzed by sterically hindered N-heterocyclic carbene
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134951openalex-snapshot
Cs2CO3 catalyzed direct tandem Michael/Michael reaction of deconjugated butenolides with α′-substituted α, β-unsaturated enones for the synthesis of fused-ring γ-butyrolactone derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2025.135129openalex-snapshot
Tandem/domino reactions in glycoscience to access diverse glycohybrids: Recent developments and future perspective
inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.01.027openalex-snapshot
Synthesis of optically active α-benzyl paraconic acids and their esters and assignment of their absolute configuration
inferred← citeshttps://doi.org/10.1016/j.tetasy.2015.06.003openalex-snapshot
Enantioselective synthesis of 4-alkenoic acids via Pd-catalyzed allylic alkylation: stereocontrolled construction of γ and δ-lactones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.12.088openalex-snapshot
Total synthesis of (+)-blastmycinone and formal synthesis of (+)-antimycin A3b
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.06.106openalex-snapshot
Synthesis of stereodefined fused δ-hydroxy-γ-lactones from dealkylative cyclization of epoxy-diesters
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.05.130openalex-snapshot
Asymmetric synthesis of γ-lactones through reaction of sulfoxonium ylides, aldehydes, and ketenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.01.039openalex-snapshot
Synthesis of functionalized benzimidazole–butyrolactone dyads
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.04.004openalex-snapshot
The first total synthesis of phomopsolidone A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.04.046openalex-snapshot
Stereoselective synthesis of 3,4-di-substituted mercaptolactones via photoredox-catalyzed radical addition of thiophenols
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152193openalex-snapshot
Asperbutenolide A, an unusual aromatic butenolide dimer with diverse bioactivities from a marine-derived fungus Aspergillus terreus SCAU011
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152751openalex-snapshot
Brønsted acid-catalyzed Friedel-Crafts-type alkylation of arenes with α-aryl diazoacetates
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00151openalex-snapshot
Catalytic Asymmetric Synthesis of Butenolides and Butyrolactones
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00782openalex-snapshot
α-Keto Acids: Acylating Agents in Organic Synthesis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c01207openalex-snapshot
Concise Stereoselective Synthesis of β-Hydroxy-γ-lactones: (4R,5R)-4-Hydroxy-γ-decalactone from the Japanese Orange Fly and Enantiomers of Arachnid Harvestmen Isolates
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00357openalex-snapshot
Metabolic Shunting in Marine-Derived Diaporthe sp. SYSU-MS4722 Yields Diverse γ-Butyrolactone Derivatives with Anti-inflammatory Activity
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02621openalex-snapshot
Copper-Catalyzed Decarboxylative [3 + 2] Annulation of Ethynylethylene Carbonates with Azlactones: Access to γ-Butyrolactones Bearing Two Vicinal Quaternary Carbon Centers
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00101openalex-snapshot
5-Substituted-furan-2(3H)-ones in [8 + 2]-Cycloaddition with 8,8-Dicyanoheptafulvene
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00729openalex-snapshot
Palladium-Catalyzed Direct Esterification via C–H Bond Activation of Aldehydes
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01607openalex-snapshot
Enantio- and Diastereoselective Synthesis of Tricyclic Lactones Bearing Three Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02622openalex-snapshot
Asymmetric Synthesis of γ-Lactones through Koga Amine-Controlled Addition of Enediolates to α,β-Unsaturated Sulfoxonium Salts
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00794openalex-snapshot
Access to Fused Tricyclic γ-Butyrolactones, A Natural Product-like Scaffold
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00122openalex-snapshot
Organocatalytic Approach for Short Asymmetric Synthesis of (R)-Paraconyl Alcohol: Application to the Total Syntheses of IM-2, SCB2, and A-Factor γ-Butyrolactone Autoregulators
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01409openalex-snapshot
Oxidative Mannich Reactions of Tertiary Amines Using a Cu(II) 2-Quinoxalinol Salen Catalyst
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02978openalex-snapshot
Stereoselective Sequential Spirocyclopropanation/Cloke–Wilson Rearrangement Reactions for Synthesis of trans-β,γ-Disubstituted γ-Butyrolactones Using Alkylidene Meldrum’s Acid and Benzyl Halides
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c04165openalex-snapshot
Total Syntheses of Paraconic Acids and 1,10-seco-Guaianolides via a Barbier Allylation/Translactonization Cascade of 3-(Bromomethyl)-2(5H)-furanone
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01652openalex-snapshot
Asymmetric Construction of α,γ-Disubstituted α,β-Butenolides Directly from Allylic Ynoates Using a Chiral Bifunctional Phosphine Ligand Enables Cooperative Au Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03727openalex-snapshot
Total Synthesis of Polysubstituted γ-Butyrolactone Lignans (−)-Hinokinin, (−)-Bicubebin B, and (−)-Isodeoxypodophyllotoxin via Oxime Carbonate Formation
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03800openalex-snapshot
Nickel Carbene-Mediated One-Carbon Homologative γ-Butyrolactonization
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00898openalex-snapshot
Metal-Catalyst-Controlled Divergent Synthesis of γ-Butyrolactones via Intramolecular Coupling of Epoxides with Alcohols
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00545openalex-snapshot
Diastereoselective Synthesis of γ-Lactones through Reaction of Enediolates with α,β-Unsaturated Sulfoxonium Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02403openalex-snapshot
Enantioselective Synthesis of γ-Butyrolactones Bearing γ-Quaternary Stereocenters via Nickel-Catalyzed Reductive Coupling of Acrylates with Ketones
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03595openalex-snapshot
Palladium-Catalyzed Cascade Reaction Involving Cyclopropenones Enables Construction of Heterocycle-Containing γ-alkylidenebutenolides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03691openalex-snapshot
Cobalt-Catalyzed Intramolecular Fluoroalkylative Carbonylation of Unactivated Alkenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03631openalex-snapshot
Chiral Hypervalent Iodine(III) Catalyst Promotes Highly Enantioselective Sulfonyl- and Phosphoryl-oxylactonizations
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02688openalex-snapshot
Nucleo-Palladation-Triggering Alkene Functionalization: A Route to γ-Lactones
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01063openalex-snapshot
Catalytic Dehydrative Lactonization of Allylic Alcohols
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03796openalex-snapshot
Site-Selective and Enantioselective α,β,γ-Functionalization of 5-Alkylidenefuran-2(5H)-ones: A Route to Polycyclic γ-Lactones
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00521openalex-snapshot
A Sequential Pd-AAA/Cross-Metathesis/Cope Rearrangement Strategy for the Stereoselective Synthesis of Chiral Butenolides
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01893openalex-snapshot
Iodine(III)-Mediated Contraction of 3,4-Dihydropyranones: Access to Polysubstituted γ-Butyrolactones
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02658openalex-snapshot
Dinuclear Zinc-Catalyzed Asymmetric Tandem Reaction of α-Hydroxy-1-indanone: Access to Spiro[1-indanone-5,2′-γ-butyrolactones]
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02705openalex-snapshot
Calcium(II)- and Triflimide-Catalyzed Intramolecular Hydroacyloxylation of Unactivated Alkenes in Hexafluoroisopropanol
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02848openalex-snapshot
Synthesis of γ-Lactones via the Kowalski Homologation Reaction: Protecting-Group-Free Divergent Total Syntheses of Eupomatilones-2,5,6, and 3-epi-Eupomatilone-6
inferred← citeshttps://doi.org/10.1021/acscatal.3c04900openalex-snapshot
Iron-Catalyzed Intramolecular C(sp 3 )-H Lactonization of Hydroxamate Derivatives Promoted by a 1,5-HAT
inferred← citeshttps://doi.org/10.1021/acscatal.5c00764openalex-snapshot
Benzophenothiazine/Boronic Acid Cooperative Photocatalysis Enables the Synthesis of γ-Lactones via the [3 + 2] Cycloaddition of α,β-Unsaturated Carboxylic Acids with Olefins
inferred← citeshttps://doi.org/10.1021/acscatal.9b00840openalex-snapshot
Enantioselective Epoxidation of β,γ-Unsaturated Carboxylic Acids by a Cooperative Binuclear Titanium Complex
inferred← citeshttps://doi.org/10.1021/acscatal.9b04405openalex-snapshot
Stereoconvergent Conjugate Addition of Arylboronic Acids to α-Angelica Lactone Derivatives: Synthesis of Stereochemically Complex γ-Butyrolactones
inferred← citeshttps://doi.org/10.1021/bi101858gopenalex-snapshot
Protein Reactivity of Natural Product-Derived γ-Butyrolactones
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1021/ja061146mopenalex-snapshot
The Oxidative Mannich Reaction Catalyzed by Dirhodium Caprolactamate
inferred← citeshttps://doi.org/10.1021/ja210149gopenalex-snapshot
Enantioselective Synthesis of Branched Allylic Esters via Rhodium-Catalyzed Coupling of Allenes with Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/ja309635wopenalex-snapshot
Direct Catalytic Anti-Markovnikov Hydroetherification of Alkenols
inferred← citeshttps://doi.org/10.1021/ja402479ropenalex-snapshot
Simple and Sustainable Iron-Catalyzed Aerobic C–H Functionalization of N,N-Dialkylanilines
inferred← citeshttps://doi.org/10.1021/ja406356copenalex-snapshot
Enantioselective α-Alkenylation of Aldehydes with Boronic Acids via the Synergistic Combination of Copper(II) and Amine Catalysis
inferred← citeshttps://doi.org/10.1021/ja502167hopenalex-snapshot
Dehydrogenative α-Oxygenation of Ethers with an Iron Catalyst
inferred← citeshttps://doi.org/10.1021/ja809610hopenalex-snapshot
Asymmetric 1,4-Dihydroxylation of 1,3-Dienes by Catalytic Enantioselective Diboration
inferred← citeshttps://doi.org/10.1021/jacs.2c12995openalex-snapshot
Enantio- and Diastereoselective De Novo Synthesis of 3-Substituted Proline Derivatives via Cooperative Photoredox/Brønsted Acid Catalysis and Epimerization
inferred← citeshttps://doi.org/10.1021/jacs.3c01404openalex-snapshot
A Catalytic Asymmetric Hydrolactonization
inferred← citeshttps://doi.org/10.1021/jacs.4c03617openalex-snapshot
Kinetic Resolution of β-Branched Aldehydes through Peptide-Catalyzed Conjugate Addition Reactions
inferred← citeshttps://doi.org/10.1021/jacs.4c04376openalex-snapshot
Transition Metal-Mimicking Relay Catalysis by a Low-Valent Phosphorus Compound
inferred← citeshttps://doi.org/10.1021/jacs.5b01131openalex-snapshot
Enantioselective Redox-Neutral Rh-Catalyzed Coupling of Terminal Alkynes with Carboxylic Acids Toward Branched Allylic Esters
inferred← citeshttps://doi.org/10.1021/jacs.5b08019openalex-snapshot
Ruthenium Catalyzed Diastereo- and Enantioselective Coupling of Propargyl Ethers with Alcohols: Siloxy-Crotylation via Hydride Shift Enabled Conversion of Alkynes to π-Allyls
inferred← citeshttps://doi.org/10.1021/jacs.5c01988openalex-snapshot
Phenothiazine Sulfoxides as Active Photocatalysts for the Synthesis of γ-Lactones
inferred← citeshttps://doi.org/10.1021/jacs.5c07358openalex-snapshot
Enantioselective Construction of β-Substituted γ-Lactone through Catalytic Asymmetric Oshima–Utimoto Reaction: Divergent Total Syntheses of (−)-Podophyllotoxin and Its Eleven Congeners
inferred← citeshttps://doi.org/10.1021/jf070305yopenalex-snapshot
A Convenient Route to the Synthesis of Isotopomeric Dihydro-2(3H)furanones
inferred← citeshttps://doi.org/10.1021/jo0619128openalex-snapshot
Facile Chemo-, Regio-, and Diastereoselective Approach to cis-3,5-Disubstituted γ-Butyrolactones and Fused γ-Butyrolactones
inferred← citeshttps://doi.org/10.1021/jo2021218openalex-snapshot
Sonogashira Coupling Reactions of Bromomaleimides: Route to Alkyne/cis-Alkene/Alkyl Maleimides: Synthesis of Luffarin X and Cacospongionolide C
inferred← citeshttps://doi.org/10.1021/jo400177jopenalex-snapshot
An Asymmetric Synthesis of trans-Fused Butyrolactones from Endoperoxides
inferred← citeshttps://doi.org/10.1021/jo4003213openalex-snapshot
Diastereoselective Reaction of Sulfoxonium Ylides, Aldehydes and Ketenes: An Approach to trans-γ-Lactones
inferred← citeshttps://doi.org/10.1021/jo8018285openalex-snapshot
A Regio- and Diastereoselective Intramolecular Nitrone Cycloaddition for Practical 3- and 2,3-Disubstituted Piperidine Synthesis from γ-Butyrolactone
inferred← citeshttps://doi.org/10.1021/jo900810aopenalex-snapshot
Asymmetric Syntheses of (−)-Enterolactone and (7′R)-7′-Hydroxyenterolactone via Organocatalyzed Aldol Reaction
inferred← citeshttps://doi.org/10.1021/ol0706408openalex-snapshot
An Efficient Oxidative Lactonization of 1,4-Diols Catalyzed by Cp*Ru(PN) Complexes
inferred← citeshttps://doi.org/10.1021/ol201322wopenalex-snapshot
Concise Total Synthesis of (−)-8-Epigrosheimin
inferred← citeshttps://doi.org/10.1021/ol2033493openalex-snapshot
A New Synthesis of γ-Butyrolactones via AuCl 3 - or Hg(II)-Catalyzed Intramolecular Hydroalkoxylation of 4-Bromo-3-yn-1-ols
inferred← citeshttps://doi.org/10.1021/ol502148aopenalex-snapshot
Straightforward Enantioselective Access to γ-Butyrolactones Bearing an All-Carbon β-Quaternary Stereocenter
inferred← citeshttps://doi.org/10.1021/ol5022993openalex-snapshot
Butyrolactone Synthesis via Polar Radical Crossover Cycloaddition Reactions: Diastereoselective Syntheses of Methylenolactocin and Protolichesterinic Acid
inferred← citeshttps://doi.org/10.1021/prechem.3c00117openalex-snapshot
γ-Butyrolactone Synthesis from Allylic Alcohols Using the CO2 Radical Anion
inferred← citeshttps://doi.org/10.1038/s41467-023-44336-2openalex-snapshot
Modular access to chiral bridged piperidine-γ-butyrolactones via catalytic asymmetric allylation/aza-Prins cyclization/lactonization sequences
inferred← citeshttps://doi.org/10.1038/s41598-017-12030-1openalex-snapshot
Local order and vibrational coupling of the C=O Stretching Mode of γ-Caprolactone in liquid binary mixtures
inferred← citeshttps://doi.org/10.1038/s41929-019-0387-3openalex-snapshot
Diastereodivergent synthesis of enantioenriched α,β-disubstituted γ-butyrolactones via cooperative N-heterocyclic carbene and Ir catalysis
inferred← citeshttps://doi.org/10.1038/s42004-026-01972-1openalex-snapshot
Divergent synthesis of γ-lactones and cyclopropanes via efficient [1 + 4] and [1 + 2] annulations of amide-sulfoxonium ylides
inferred← citeshttps://doi.org/10.1039/b909418kopenalex-snapshot
Enantioselective synthesis of Anomala osakana pheromone and Janus integer pheromone: a flexible approach to chiral γ-butyrolactones
inferred← citeshttps://doi.org/10.1039/c1ob05113jopenalex-snapshot
Stereoselective routes to aryl substituted γ-butyrolactones and their application towards the synthesis of highly oxidised furanocembranoids
inferred← citeshttps://doi.org/10.1039/c1ob05709jopenalex-snapshot
Regio- and stereoselective selenium dioxide allylic oxidation of (E)-dialkyl alkylidenesuccinates to (Z)-allylic alcohols: Synthesis of natural and unnatural butenolides
inferred← citeshttps://doi.org/10.1039/c2cc18172jopenalex-snapshot
Enantioselective synthesis of (−)-paeonilide
inferred← citeshttps://doi.org/10.1039/c2cc32147eopenalex-snapshot
Catalytic, enantio- and diastereoselective synthesis of γ-butyrolactones incorporating quaternary stereocentres
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