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Influence of Reactant Polarity on the Course of the Inverse-Electron-Demand Diels−Alder Reaction. A DFT Study of Regio- and Stereoselectivity, Presence of Lewis Acid Catalyst, and Inclusion of Solvent Effects in the Reaction between Nitroethene and Substituted Ethenes
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Density functional study of Diels-Alder reactions between cyclopentadiene and substituted derivatives of ethylene
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PM3 study of the domino reaction of nitroalkenes with silyl enol ethers
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Mechanistic Aspects of Diels‐Alder Reactions: A Critical Survey
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Mechanism of the Hetero‐Diels–Alder Reaction of Oxadienes and Alkenes: Calculation of the Acrolein/Ethene System
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Transition Structures of Hydrocarbon Pericyclic Reactions
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Hydrophobic Effects. Opinions and Facts
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Intermolecular [4 + 2]‐Cycloadditions of Nitroalkenes with Cyclic Olefins. Transformations of Cyclic Nitronates
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Optimization of equilibrium geometries and transition structures
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Frontier Orbitals and Organic Chemical Reactions
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Application of the pople-santry-segal CNDO method to the cyclopropylcarbinyl and cyclobutyl cation and to bicyclobutane
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Theoretical Study of the Reaction of Dimethyl Acetylenedicarboxylate with 1-Methyl-2-(1-substituted vinyl)pyrroles
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Theoretical study of the solvent effects on the mechanisms of addition of dimethyl acetylenedicarboxylate to 1-methyl-2-vinylpyrrole
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Synthesis of 2-nitro 1,3-dienes. Useful intermediates in the preparation of unsaturated 1,4-dicarbonyl compounds
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Reactivity and selectivity in catalyzed diels-alder reactions
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Rationalization of the catalytic effect on the reactivity—selectivity relationship in diels—alder reactions
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Bond order rearrangements during chemical reactions
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Density-functional theory of atoms and molecules
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Cycloaddition Reactions in Organic Synthesis
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Hetero Diels—Alder Methodology in Organic Synthesis
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Pericyclic Reaction Transition States: Passions and Punctilios, 1935-1995
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Molecular Interactions in Solution: An Overview of Methods Based on Continuous Distributions of the Solvent
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Tandem [4+2]/[3+2] Cycloadditions of Nitroalkenes
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Characterization of the progress of chemical reactions by ab initio bond orders
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Solvent effects on a Diels-Alder reaction from computer simulations
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Solvent effects on the mechanism and selectivities of asymmetric Diels-Alder reactions
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Theoretical Secondary Kinetic Isotope Effects and the Interpretation of Transition State Geometries. 2. The Diels-Alder Reaction Transition State Geometry
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Fine Tuning [4 + 2] and [2 + 4] Diels-Alder Reactions Catalyzed by Lewis Acids
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Transition structures of the Lewis acid-catalyzed Diels-Alder reaction of butadiene with acrolein. The origins of selectivity
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MC-SCF study of the Diels-Alder reaction between ethylene and butadiene
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Density Functional Theory Prediction of the Relative Energies and Isotope Effects for the Concerted and Stepwise Mechanisms of the Diels−Alder Reaction of Butadiene and Ethylene
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Influence of Reactant Polarity on the Course of (4 + 2) Cycloadditions
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Density Functional Theory Study of a Lewis Acid Catalyzed Diels−Alder Reaction. The Butadiene + Acrolein Paradigm
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Hetero-Diels-Alder reaction transition structures: reactivity, stereoselectivity, catalysis, solvent effects, and the exo-lone-pair effect
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Theoretical Study of Ethylene and Vinyl Alcohol Addition to 1,4-Dioxa-1,3-butadiene
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Ab Initio Study of the Thermal and Lewis Acid-Catalyzed Hetero Diels-Alder Reactions of 1,3-Butadiene and Isoprene with Sulfur Dioxide
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Influence of Alkyl Substituent on the Asynchronous Transition Structure of Boron-Catalyzed Diels-Alder Cycloaddition of .alpha.,.beta.-Unsaturated Aldehydes with 1,1-Dimethyl-1,3-butadiene Derivatives
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Electronic factors influencing the activation barrier of the Diels-Alder reaction. An ab initio study
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Effect of Lewis Acid Catalysis on the Diels−Alder Reaction between Methyl (Z)-(S)-4,5-(2,2-Propylidenedioxy)pent-2-enoate and Cyclopentadiene. A Theoretical Study
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Modelling of solvent effects on the Diels–Alder reaction
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Investigation of solvent effects on pericyclic reactions by computer simulations
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Ab initio study of heterodienophile addition to oxazole
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DFT study of the Diels–Alder reactions between ethylene with buta-1,3-diene and cyclopentadiene
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Hartree–Fock second derivatives and electric field properties in a solvent reaction field: Theory and application
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Density-functional thermochemistry. III. The role of exact exchange
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Density functional transition states of organic and organometallic reactions
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Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density
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CRC Handbook of Chemistry and Physics
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/j.theochem.2007.12.004openalex-snapshot
Mechanistic details of the domino reaction of nitronaphthalenes with the electron-rich dienes. A DFT study
inferred← citeshttps://doi.org/10.1016/j.theochem.2009.06.018openalex-snapshot
A competition between carbo and hetero Diels–Alder reactions of E-2-phenyl-1-cyano-1-nitroethene to cyclopentadiene in the light of B3LYP/6-31G(d) computational study
inferred← citeshttps://doi.org/10.1016/j.theochem.2009.08.015openalex-snapshot
Substituent effects of α,β-unsaturated aldehyde compounds in inverse electron demand Hetero-Diels–Alder reactions: A theoretical study
inferred← citeshttps://doi.org/10.1016/j.theochem.2009.11.028openalex-snapshot
A DFT study of the role of the Mg complex formation on the mechanism of the 1,3-dipolar cycloadditions of benzonitrile oxides with acryloylpyrazolidinone
inferred← citeshttps://doi.org/10.1016/j.theochem.2010.02.023openalex-snapshot
Reactivity of (E)-2-aryl-1-cyano-1-nitroethenes in carbo and hetero Diels–Alder reactions with cyclopentadiene: A DFT study
inferred← citeshttps://doi.org/10.1016/s0040-4020(00)00989-3openalex-snapshot
Theoretical study on the mechanism of the domino reactions of tertiary α-cyano-enamines and dimethyl acetylenedicarboxylate
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00464-1openalex-snapshot
A theoretical study of the selectivity for the domino [5+2]/[4+2] cycloadditions of γ-pyrones bearing tethered alkenes with substituted 1,3-butadienes
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)00326-5openalex-snapshot
A density functional theory study for the Diels–Alder reaction between N-acyl-1-aza-1,3-butadienes and vinylamines. Lewis acid catalyst and solvent effects
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)00410-6openalex-snapshot
Quantitative characterization of the global electrophilicity power of common diene/dienophile pairs in Diels–Alder reactions
inferred← citeshttps://doi.org/10.1016/s0040-4020(03)00547-7openalex-snapshot
A DFT study on the 1,3-dipolar cycloaddition reactions of C-(methoxycarbonyl)-N-methyl nitrone with methyl acrylate and vinyl acetate
inferred← citeshttps://doi.org/10.1016/s0166-1280(01)00370-0openalex-snapshot
A PM3 study of the molecular mechanism for the cycloaddition between cyclopentadiene and protonated pyridine-imine derivatives
inferred← citeshttps://doi.org/10.1016/s1380-7323(07)80010-0openalex-snapshot
Chapter 9 The electrophilicity index in organic chemistry
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.2c00549openalex-snapshot
Understanding the Mechanism of Diels–Alder Reactions with Anionic Dienophiles: A Systematic Comparison of [ECX] − (E = P, As; X = O, S, Se) Anions
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01801openalex-snapshot
Lithium Cation-Catalyzed Benzene Diels–Alder Reaction: Insights on the Molecular Mechanism Within the Molecular Electron Density Theory
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00843openalex-snapshot
Cycloadditions of 4-Alkenyl-2-aminothiazoles with Nitroalkenes in the Formal Synthesis of Pramipexole: An Experimental and Computational Study
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01297openalex-snapshot
Understanding the Electronic Effects of Lewis Acid Catalysts in Accelerating Polar Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02872openalex-snapshot
Cycloaddition Reactions of Indanedioneketene with Electron-Rich Dienophiles: An Experimental and a Theoretical Study
inferred← citeshttps://doi.org/10.1021/acs.jpcc.7b07402openalex-snapshot
Tandem Aromatization of Oxygenated Furans by Framework Zinc In Zeolites. A Computational Study
inferred← citeshttps://doi.org/10.1021/acscatal.6b02682openalex-snapshot
Catalysis of the Diels–Alder Reaction of Furan and Methyl Acrylate in Lewis Acidic Zeolites
inferred← citeshttps://doi.org/10.1021/acscatal.8b03664openalex-snapshot
Lewis Acid Site and Hydrogen-Bond-Mediated Polarization Synergy in the Catalysis of Diels–Alder Cycloaddition by Band-Gap Transition-Metal Oxides
inferred← citeshttps://doi.org/10.1021/acsomega.4c07888openalex-snapshot
DFT Investigation of the Stereoselectivity of the Lewis-Acid-Catalyzed Diels–Alder Reaction between 2,5-Dimethylfuran and Acrolein
inferred← citeshttps://doi.org/10.1021/cr990052aopenalex-snapshot
Theoretical Methods for the Description of the Solvent Effect in Biomolecular Systems
inferred← citeshttps://doi.org/10.1021/cr990410+openalex-snapshot
Salt Effects on Diels−Alder Reaction Kinetics
inferred← citeshttps://doi.org/10.1021/ja068527kopenalex-snapshot
The Participation of Alkynylboronates in Inverse Electron Demand [4 + 2] Cycloadditions: A Mechanistic Study
inferred← citeshttps://doi.org/10.1021/jo000061fopenalex-snapshot
Toward an Understanding of the Mechanisms of the Intramolecular [5 + 2] Cycloaddition Reaction of γ-Pyrones Bearing Tethered Alkenes. A Theoretical Study
inferred← citeshttps://doi.org/10.1021/jo001332popenalex-snapshot
A Theoretical Study of the Molecular Mechanism of the Reaction between N,N-Dimethylmethyleneammonium Cation and Cyclopentadiene
inferred← citeshttps://doi.org/10.1021/jo0015422openalex-snapshot
A Theoretical Study of the Reaction between Cyclopentadiene and Protonated Imine Derivatives: A Shift from a Concerted to a Stepwise Molecular Mechanism
inferred← citeshttps://doi.org/10.1021/jo010243popenalex-snapshot
Aromatic Dienophiles. 1. A Theoretical Study of an Inverse-Electron Demand Diels−Alder Reaction between 2-Aminopyrrole and 1,3,5-Triazine
inferred← citeshttps://doi.org/10.1021/jo011003copenalex-snapshot
Density Functional Theory Study of the Cycloaddition Reaction of Furan Derivatives with Masked o-Benzoquinones. Does the Furan Act as a Dienophile in the Cycloaddition Reaction?
inferred← citeshttps://doi.org/10.1021/jo016175oopenalex-snapshot
Cyclic Vinyl p-Tolyl Sulfilimines as Chiral Dienophiles: Theoretical Study on the Stereoselectivity, Lewis Acid Catalysis, and Solvent Effects in Their Diels−Alder Reactions
inferred← citeshttps://doi.org/10.1021/jo030156sopenalex-snapshot
Enhancing Reactivity of Carbonyl Compounds via Hydrogen-Bond Formation. A DFT Study of the Hetero-Diels−Alder Reaction between Butadiene Derivative and Acetone in Chloroform
inferred← citeshttps://doi.org/10.1021/jo0479213openalex-snapshot
A DFT Study of Diels−Alder Reactions of o-Quinone Methides and Various Substituted Ethenes: Selectivity and Reaction Mechanism
inferred← citeshttps://doi.org/10.1021/jo051958lopenalex-snapshot
Theoretical Study of Reactant Activation in 1,3-Dipolar Cycloadditions of Cyclic Nitrones to Free and Pt-Bound Nitriles
inferred← citeshttps://doi.org/10.1021/jo3027017openalex-snapshot
Why Do Five-Membered Heterocyclic Compounds Sometimes Not Participate in Polar Diels–Alder Reactions?
inferred← citeshttps://doi.org/10.1021/jo401482bopenalex-snapshot
Selectivities of Multicomponent [4 + 2]/[3 + 2] Cycloadditions of 3-Nitroindole with Substituted Alkenes: A DFT Analysis
inferred← citeshttps://doi.org/10.1021/jo5025514openalex-snapshot
Activation-Strain Analysis Reveals Unexpected Origin of Fast Reactivity in Heteroaromatic Azadiene Inverse-Electron-Demand Diels–Alder Cycloadditions
inferred← citeshttps://doi.org/10.1021/jo800572aopenalex-snapshot
Understanding the Reactivity of Captodative Ethylenes in Polar Cycloaddition Reactions. A Theoretical Study
inferred← citeshttps://doi.org/10.1021/jo801575gopenalex-snapshot
Understanding the Participation of Quadricyclane as Nucleophile in Polar [2σ + 2σ + 2π] Cycloadditions toward Electrophilic π Molecules
inferred← citeshttps://doi.org/10.1021/jo802822uopenalex-snapshot
Toward an Understanding of the Unexpected Regioselective Hetero-Diels−Alder Reactions of Asymmetric Tetrazines with Electron-Rich Ethylenes: A DFT Study
inferred← citeshttps://doi.org/10.1021/jo9912911openalex-snapshot
A Convenient Preparation of N-Acyl-1-aza-1,3-diene from β-Formylenamide and Its Utility in Inverse Electron Demand Diels−Alder Reactions
inferred← citeshttps://doi.org/10.1021/jo991507zopenalex-snapshot
A DFT Study of the Domino Inter [4 + 2]/Intra [3 + 2] Cycloaddition Reactions of Nitroalkenes with Enol Ethers
inferred← citeshttps://doi.org/10.1021/jp012603iopenalex-snapshot
Density Functional Theory Study for the Cycloaddition of 1,3-Butadienes with Dimethyl Acetylenedicarboxylate. Polar Stepwise vs Concerted Mechanisms
inferred← citeshttps://doi.org/10.1021/jp020715jopenalex-snapshot
Quantitative Characterization of the Local Electrophilicity of Organic Molecules. Understanding the Regioselectivity on Diels−Alder Reactions
inferred← citeshttps://doi.org/10.1021/jp035261kopenalex-snapshot
1,3-Dipolar Cycloaddition of Nitrones to Free and Pt-Bound Nitriles. A Theoretical Study of the Activation Effect, Reactivity, and Mechanism
inferred← citeshttps://doi.org/10.1021/jp063714qopenalex-snapshot
Density Functional Theory Investigation of Product Distribution following Reaction of Acrylonitrile on Diamond (001)-2×1 Surface
inferred← citeshttps://doi.org/10.1021/jp504972ropenalex-snapshot
Reactivity and Selectivity of Boron-Substituted Alkenes in the Diels–Alder Reaction with Cyclopentadiene. A Study of the Electron Charge Density and Its Laplacian
inferred← citeshttps://doi.org/10.1021/jp711704mopenalex-snapshot
An Understanding of the Electrophilic/Nucleophilic Behavior of Electro-Deficient 2,3-Disubstituted 1,3-Butadienes in Polar Diels−Alder Reactions. A Density Functional Theory Study
inferred← citeshttps://doi.org/10.1021/jp9088222openalex-snapshot
Theoretical Evaluation of Global and Local Electrophilicity Patterns to Characterize Hetero-Diels−Alder Cycloaddition of Three-Membered 2H-Azirine Ring System
inferred← citeshttps://doi.org/10.1021/jp909670wopenalex-snapshot
DFT Study of Intermolecular [4 + 2] versus [3 + 2] Cycloadditions in the Dimerization of 2,4,6-Trinitrotoluene (TNT): Regioselectivity and Stereoselectivity
inferred← citeshttps://doi.org/10.1021/jp992579xopenalex-snapshot
A DFT Characterization of the Mechanism for the Cycloaddition Reaction between 2-Methylfuran and Acetylenedicarboxylic Acid
inferred← citeshttps://doi.org/10.1039/b909611fopenalex-snapshot
Understanding the mechanism of polar Diels–Alder reactions
inferred← citeshttps://doi.org/10.1039/b925441bopenalex-snapshot
CDASE—A reliable scheme to explain the reactivity sequence between Diels–Alder pairs
inferred← citeshttps://doi.org/10.1039/c1ob05493gopenalex-snapshot
A theoretical study of imine-ene reaction influencing factors
inferred← citeshttps://doi.org/10.1039/c2ob25152copenalex-snapshot
Origin of the synchronicity in bond formation in polar Diels–Alder reactions: an ELF analysis of the reaction between cyclopentadiene and tetracyanoethylene
inferred← citeshttps://doi.org/10.1039/c2ob26442kopenalex-snapshot
Experimental and theoretical study of the [3 + 2] cycloaddition of carbonyl ylides with alkynes
inferred← citeshttps://doi.org/10.1039/c2ra22886fopenalex-snapshot
Understanding the local reactivity in polar organic reactions through electrophilic and nucleophilic Parr functions
inferred← citeshttps://doi.org/10.1039/c3ob41571fopenalex-snapshot
[4 + 3] and [4 + 2] mechanisms of the Diels–Alder reactions of vinylboranes: an analysis of the electron charge density distribution
inferred← citeshttps://doi.org/10.1039/c3ob41628copenalex-snapshot
Unraveling polar Diels–Alder reactions with conceptual DFT analysis and the distortion/interaction model
inferred← citeshttps://doi.org/10.1039/c3ra40929eopenalex-snapshot
Understanding C–C bond formation in polar reactions. An ELF analysis of the Friedel–Crafts reaction between indoles and nitroolefins
inferred← citeshttps://doi.org/10.1039/c4ra04280hopenalex-snapshot
A new C–C bond formation model based on the quantum chemical topology of electron density
inferred← citeshttps://doi.org/10.1039/c5ra08307aopenalex-snapshot
Simple descriptors for assessing the outcome of aza-Diels–Alder reactions
inferred← citeshttps://doi.org/10.1039/c5ra13527copenalex-snapshot
Understanding the molecular mechanism in a regiospecific [3 + 2] cycloaddition reaction including C–O and C–S interactions: an ELF topological analysis
inferred← citeshttps://doi.org/10.1039/c5ra17778bopenalex-snapshot
Ionic Diels–Alder reaction of 3-bromofuran toward the highly electron deficient cyclobuteniminium cation: a regio- and stereoselectivity, and molecular mechanism study using DFT
inferred← citeshttps://doi.org/10.1039/c6ob00815aopenalex-snapshot
A mechanistic insight into the effect of piperidine as an organocatalyst on the [3 + 2] cycloaddition reaction of benzalacetone with phenyl azide from a computational study
inferred← citeshttps://doi.org/10.1039/c9nj00269copenalex-snapshot
Copper( i )-catalyzed asymmetric aza Diels–Alder reactions of azoalkenes toward fulvenes: a molecular electron density theory study
inferred← citeshttps://doi.org/10.1039/d1nj04962copenalex-snapshot
A molecular electron density theory study of the higher-order cycloaddition reactions of tropone with electron-rich ethylenes. The role of the Lewis acid catalyst in the mechanism and pseudocyclic selectivity
inferred← citeshttps://doi.org/10.1039/d5cp02448jopenalex-snapshot
Molecular density functional theory with atomistic dipolar solvent to study pressure effect on a Diels–Alder reaction
inferred← citeshttps://doi.org/10.1039/d6nj00643dopenalex-snapshot
A new, comprehensive insight into the competition between [4+2] and [2+4] cycloaddition schemes and molecular mechanism of the Diels–Alder reaction of 2-nitrofuran with isoprene
inferred← citeshttps://doi.org/10.1039/d6ra02126copenalex-snapshot
Electrophilic allenes participate in polar Diels–Alder reactions: study of the reactivity and site-, regio- and stereoselectivity from a molecular electron density theory perspective
inferred← citeshttps://doi.org/10.1080/10406638.2022.2144910openalex-snapshot
A Molecular Electron Density Theory Study of the Polar Diels-Alder Reaction of Naphtoquinone:Cr(CO) 3 Complex with Cyclic Dienes
inferred← citeshttps://doi.org/10.1080/10406638.2023.2212102openalex-snapshot
The Diels–Alder Reaction between Euparin and Dimethyl Acetylenedicarboxylate; a Joint Experimental and Density Functional Theory Study
inferred← citeshttps://doi.org/10.1080/10426507.2017.1290626openalex-snapshot
Triethylsulfonium and triethylphosphonium cations as novel catalysts for the decomposition process of nitroethyl benzoates
inferred← citeshttps://doi.org/10.1134/s0036023606100147openalex-snapshot
Theoretical study of 1,3-dipolar cycloaddition of nitrones to doubly activated nitriles
inferred← citeshttps://doi.org/10.1134/s107036320902011xopenalex-snapshot
Theoretical study of ammonia nucleophilic addition to nitriles in platinum complexes
inferred← citeshttps://doi.org/10.1139/v06-013openalex-snapshot
Concerted and stepwise mechanisms in the DielsAlder and Michael reactions of furans with methyl 3-nitroacrylate Experimental and theoretical studies
inferred← citeshttps://doi.org/10.17344/acsi.2014.305openalex-snapshot
Theoretical analysis of the mechanism and regioselectivity of the 1, 3-dipolar cycloaddition of E-3-(dimethylamino)-1-(10H-phenothiazin-2-yl)prop-2-en-1-one with some nitrilimines using DFT and the distortion/interaction model
inferred← citeshttps://doi.org/10.2174/138527212803520263openalex-snapshot
Understanding the Bond Formation in Hetero-Diels-Alder Reactions. An ELF Analysis of the Reaction of Nitroethylene with Dimethylvinylamine
inferred← citeshttps://doi.org/10.2478/s11532-013-0276-6openalex-snapshot
An experimental and theoretical study of the polar [2+3] cycloaddition reactions between 1-chloro-1-nitroethene and (Z)-C-aryl-N-phenylnitrones
inferred← citeshttps://doi.org/10.3184/146867816x14506899861213openalex-snapshot
DFT study on the mechanism of the Diels–Alder reactions leading to bicyclo[4.2.0]octenones
inferred← citeshttps://doi.org/10.3389/fchem.2019.00446openalex-snapshot
Theoretical Insights Into the Depolymerization Mechanism of Lignin to Methyl p-hydroxycinnamate by [Bmim][FeCl4] Ionic Liquid
inferred← citeshttps://doi.org/10.3390/chemistry3030061openalex-snapshot
Unveiling the Intramolecular Ionic Diels–Alder Reactions within Molecular Electron Density Theory
inferred← citeshttps://doi.org/10.3390/chemistry4030052openalex-snapshot
Unveiling the Chemistry of Higher-Order Cycloaddition Reactions within the Molecular Electron Density Theory
inferred← citeshttps://doi.org/10.3390/molecules21101319openalex-snapshot
Molecular Electron Density Theory: A Modern View of Reactivity in Organic Chemistry
inferred← citeshttps://doi.org/10.3390/molecules25112535openalex-snapshot
Unveiling the Lewis Acid Catalyzed Diels–Alder Reactions Through the Molecular Electron Density Theory
inferred← citeshttps://doi.org/10.3390/molecules26123638openalex-snapshot
Unveiling the Ionic Diels–Alder Reactions within the Molecular Electron Density Theory
inferred← citeshttps://doi.org/10.3390/molecules31152725openalex-snapshot
A Molecular Electron Density Theory Study of the Domino [4+2]/[3+2] Cycloaddition Leading to a Tricyclic 1,2-Oxazine Nitrones
inferred← citeshttps://doi.org/10.3987/rev-21-955openalex-snapshot
The Fascinating Chemistry of Mesoionic 4-Trifluoroacetyl-1,3-oxazolium-5-olates and Related Compounds
inferred← citeshttps://doi.org/10.5267/j.ccl.2016.11.001openalex-snapshot
DFT study of the decomposition reactions of nitroethyl benzoates catalyzed by the 1,3-dimethylimidazolium cation
inferred← citeshttps://doi.org/10.58088/2naw-f504openalex-snapshot
Computational studies on the catalyzed conversion of furans to aromatics
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