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Branching Out from the Bisabolyl Cation. Unifying Mechanistic Pathways to Barbatene, Bazzanene, Chamigrene, Chamipinene, Cumacrene, Cuprenene, Dunniene, Isobazzanene, Iso-γ-bisabolene, Isochamigrene, Laurene, Microbiotene, Sesquithujene, Sesquisabinene, Thujopsene, Trichodiene, and Widdradiene…

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What this work says

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

inferredcites →https://doi.org/10.1002/1521-3773(20020104)41:1<48::aid-anie48>3.0.co;2-uopenalex-snapshot

The Hydrogen Bond in the Solid State

inferredcites →https://doi.org/10.1002/3527605746.ch6openalex-snapshot

Theozymes and Catalyst Design

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The Concerted Nature of the Cyclization of Squalene Oxide to the Protosterol Cation

inferredcites →https://doi.org/10.1002/cbic.201100268openalex-snapshot

Biosynthesis of Sesquiterpenes by the Fungus Fusarium verticillioides

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Theoretical and Experimental Analysis of the Reaction Mechanism of MrTPS2, a Triquinane‐Forming Sesquiterpene Synthase from Chamomile

inferredcites →https://doi.org/10.1002/poc.1320openalex-snapshot

Recent excursions to the borderlands between the realms of concerted and stepwise: carbocation cascades in natural products biosynthesis

inferredcites →https://doi.org/10.1002/wcms.6openalex-snapshot

Hyperconjugation

inferredcites →https://doi.org/10.1007/3-540-48146-x_2openalex-snapshot

Cyclization Enzymes in the Biosynthesis of Monoterpenes, Sesquiterpenes, and Diterpenes

inferredcites →https://doi.org/10.1007/978-1-4613-4118-5openalex-snapshot

The Nonclassical Ion Problem

inferredcites →https://doi.org/10.1016/b978-0-08-091283-7.00039-4openalex-snapshot

Sesquiterpene Biosynthesis: Cyclization Mechanisms

inferredcites →https://doi.org/10.1016/j.abb.2005.10.011openalex-snapshot

Two pockets in the active site of maize sesquiterpene synthase TPS4 carry out sequential parts of the reaction scheme resulting in multiple products

inferredcites →https://doi.org/10.1016/j.abb.2007.06.016openalex-snapshot

Exploring biosynthetic diversity with trichodiene synthase

inferredcites →https://doi.org/10.1016/j.abb.2007.10.015openalex-snapshot

Structural and mechanistic analysis of trichodiene synthase using site-directed mutagenesis: Probing the catalytic function of tyrosine-295 and the asparagine-225/serine-229/glutamate-233– Mg2+B motif

inferredcites →https://doi.org/10.1016/j.cbpa.2007.12.008openalex-snapshot

Unearthing the roots of the terpenome

inferredcites →https://doi.org/10.1016/j.phytochem.2004.07.005openalex-snapshot

Halogenated diterpenoids from the red alga Laurencia nipponica

inferredcites →https://doi.org/10.1016/j.phytochem.2004.11.002openalex-snapshot

Sesquiterpenes from Cupressus macrocarpa foliage

inferredcites →https://doi.org/10.1016/j.tetlet.2005.06.076openalex-snapshot

Cytotoxic cuparene sesquiterpenes from Laurencia microcladia

inferredcites →https://doi.org/10.1016/s0031-9422(97)00553-0openalex-snapshot

A sesquiterpene class from Illicium dunnianum

inferredcites →https://doi.org/10.1016/s0040-4039(01)91944-6openalex-snapshot

Marine natural products X elatol, a halogenated sesquiterpene alcohol from the red alga .

inferredcites →https://doi.org/10.1016/s0040-4039(97)00193-7openalex-snapshot

The formyl CH--O hydrogen bond as a key to transition-state organization in enantioselective allylation, aldol and Diels-Alder reactions catalyzed by chiral lewis acids

inferredcites →https://doi.org/10.1016/s1367-5931(98)80112-9openalex-snapshot

Theozymes and compuzymes: theoretical models for biological catalysis

inferredcites →https://doi.org/10.1021/ar00023a006openalex-snapshot

Intramolecular dynamics for the organic chemist

inferredcites →https://doi.org/10.1021/ar00072a001openalex-snapshot

The path of chemical reactions - the IRC approach

inferredcites →https://doi.org/10.1021/ar00115a005openalex-snapshot

Isoprenoid biosynthesis. Stereochemistry of the cyclization of allylic pyrophosphates

inferredcites →https://doi.org/10.1021/ar800064fopenalex-snapshot

Exploring β-Sheet Structure and Interactions with Chemical Model Systems

inferredcites →https://doi.org/10.1021/bi050059oopenalex-snapshot

Molecular Recognition of the Substrate Diphosphate Group Governs Product Diversity in Trichodiene Synthase Mutants ,

inferredcites →https://doi.org/10.1021/bi0510476openalex-snapshot

Role of Arginine-304 in the Diphosphate-Triggered Active Site Closure Mechanism of Trichodiene Synthase,

inferredcites →https://doi.org/10.1021/cr00081a004openalex-snapshot

Biosynthesis and catabolism of monoterpenoids

inferredcites →https://doi.org/10.1021/cr00105a002openalex-snapshot

Enzymic formation of sesquiterpenes

inferredcites →https://doi.org/10.1021/cr050286wopenalex-snapshot

Structural Biology and Chemistry of the Terpenoid Cyclases

inferredcites →https://doi.org/10.1021/cr100072xopenalex-snapshot

Relevance of Weak Hydrogen Bonds in the Conformation of Organic Compounds and Bioconjugates: Evidence from Recent Experimental Data and High-Level ab Initio MO Calculations

inferredcites →https://doi.org/10.1021/cr9603744openalex-snapshot

The Cation−π Interaction

inferredcites →https://doi.org/10.1021/j100096a001openalex-snapshot

Ab Initio Calculation of Vibrational Absorption and Circular Dichroism Spectra Using Density Functional Force Fields

inferredcites →https://doi.org/10.1021/j100377a021openalex-snapshot

Reaction path following in mass-weighted internal coordinates

inferredcites →https://doi.org/10.1021/ja026850ropenalex-snapshot

Concomitant C-Ring Expansion and D-Ring Formation in Lanosterol Biosynthesis from Squalene without Violation of Markovnikov's Rule

inferredcites →https://doi.org/10.1021/ja058031nopenalex-snapshot

Theoretical Studies on Farnesyl Cation Cyclization: Pathways to Pentalenene

inferredcites →https://doi.org/10.1021/ja203342popenalex-snapshot

Physical Constraints on Sesquiterpene Diversity Arising from Cyclization of the Eudesm-5-yl Carbocation

inferredcites →https://doi.org/10.1021/ja205927uopenalex-snapshot

Probing Eudesmane Cation−π Interactions in Catalysis by Aristolochene Synthase with Non-canonical Amino Acids

inferredcites →https://doi.org/10.1021/ja9005332openalex-snapshot

Consequences of Conformational Preorganization in Sesquiterpene Biosynthesis: Theoretical Studies on the Formation of the Bisabolene, Curcumene, Acoradiene, Zizaene, Cedrene, Duprezianene, and Sesquithuriferol Sesquiterpenes

inferredcites →https://doi.org/10.1021/ja9084786openalex-snapshot

Formation of Beyerene, Kaurene, Trachylobane, and Atiserene Diterpenes by Rearrangements That Avoid Secondary Carbocations

inferredcites →https://doi.org/10.1021/ja9714245openalex-snapshot

Computational Investigations of Carbenium Ion Reactions Relevant to Sterol Biosynthesis

inferredcites →https://doi.org/10.1021/ja980505dopenalex-snapshot

Carbocation−π Interaction: Computational Study of Complexation of Methyl Cation with Benzene and Comparisons with Related Systems

inferredcites →https://doi.org/10.1021/jo01308a008openalex-snapshot

Preparation and rearrangement of trichothecane-like compounds. Synthesis of aplysin and filiformin

inferredcites →https://doi.org/10.1021/jo052053aopenalex-snapshot

Tetracoordinate Carbon as a Nucleophile? Interconversion of Carbenium Ions with Carbonium Ions Possessing Nearly Square-Pyramidal Pentacoordinate Carbons

inferredcites →https://doi.org/10.1021/jo701526xopenalex-snapshot

Perturbing the Structure of the 2-Norbornyl Cation through C−H···N and C−H···π Interactions

inferredcites →https://doi.org/10.1021/jo800868ropenalex-snapshot

Computational Studies on Biosynthetic Carbocation Rearrangements Leading to Sativene, Cyclosativene, α-Ylangene, and β-Ylangene

inferredcites →https://doi.org/10.1021/jp0568430openalex-snapshot

Multicenter Bonding in Carbocations with Tetracoordinate Protons

inferredcites →https://doi.org/10.1021/jp056965sopenalex-snapshot

Nonclassical Carbocations as C−H Hydrogen Bond Donors

inferredcites →https://doi.org/10.1021/np050096gopenalex-snapshot

Sesquiterpenes from the Red Alga Laurencia tristicha

inferredcites →https://doi.org/10.1021/np0503810openalex-snapshot

A Laurane Sesquiterpene and Rearranged Derivatives from the Chinese Red Alga Laurencia okamurai Yamada

inferredcites →https://doi.org/10.1021/ol061884fopenalex-snapshot

Which Is More Likely in Trichodiene Biosynthesis: Hydride or Proton Transfer?

inferredcites →https://doi.org/10.1021/ol103079vopenalex-snapshot

How Many Secondary Carbocations Are Involved in the Biosynthesis of Avermitilol?

inferredcites →https://doi.org/10.1021/ol300817aopenalex-snapshot

Dynamic Origin of the Stereoselectivity of a Nucleophilic Substitution Reaction

inferredcites →https://doi.org/10.1039/b513599kopenalex-snapshot

Mechanistic insights into triterpene synthesis from quantum mechanical calculations. Detection of systematic errors in B3LYP cyclization energies

inferredcites →https://doi.org/10.1039/b908738aopenalex-snapshot

Modes of inactivation of trichodiene synthase by a cyclopropane-containing farnesyldiphosphate analog

inferredcites →https://doi.org/10.1039/b917107jopenalex-snapshot

The carbocation continuum in terpene biosynthesis—where are the secondary cations?

inferredcites →https://doi.org/10.1039/c0ob00167hopenalex-snapshot

Quantum chemical dissection of the classic terpinyl/pinyl/bornyl/camphyl cation conundrum—the role of pyrophosphate in manipulating pathways to monoterpenes

inferredcites →https://doi.org/10.1039/c0sc00333fopenalex-snapshot

A tangled web—interconnecting pathways to amorphadiene and the amorphene sesquiterpenes

inferredcites →https://doi.org/10.1039/c1cc14414fopenalex-snapshot

Theoretical calculations on carbocations involved in the biosynthesis of bergamotenes and related terpenes—the same and not the same

inferredcites →https://doi.org/10.1039/c1cp20427kopenalex-snapshot

Weak H-bonds. Comparisons of CH⋯O to NH⋯O in proteins and PH⋯N to direct P⋯N interactions

inferredcites →https://doi.org/10.1039/c1cp22565kopenalex-snapshot

Do we fully understand what controls chemical selectivity?

inferredcites →https://doi.org/10.1039/c1np00006copenalex-snapshot

Biosynthesis via carbocations: Theoretical studies on terpene formation

inferredcites →https://doi.org/10.1039/c1ra00212kopenalex-snapshot

Biosynthesis of acorane sesquiterpenes by Trichoderma

inferredcites →https://doi.org/10.1039/c3np70028copenalex-snapshot

Walking in the woods with quantum chemistry – applications of quantum chemical calculations in natural products research

inferredcites →https://doi.org/10.1039/c3sc50571eopenalex-snapshot

C–H⋯π interactions as modulators of carbocation structure – implications for terpene biosynthesis

inferredcites →https://doi.org/10.1039/qr9672100331openalex-snapshot

Sesquiterpene biogenesis

inferredcites →https://doi.org/10.1055/s-2006-957643openalex-snapshot

Sesquiterpene Content of the Antibacterial Dichloromethane Extract of the Marine Red AlgaLaurencia obtusa

inferredcites →https://doi.org/10.1063/1.464304openalex-snapshot

A new mixing of Hartree–Fock and local density-functional theories

inferredcites →https://doi.org/10.1063/1.464913openalex-snapshot

Density-functional thermochemistry. III. The role of exact exchange

inferredcites →https://doi.org/10.1071/ch9921611openalex-snapshot

Tropical Marine Algae. VIII. The Structural Determination of Novel Sesquiterpenoid Metabolites From the Red Alga .Laurencia majuscula

inferredcites →https://doi.org/10.1073/pnas.1209316109openalex-snapshot

Dynamics, transition states, and timing of bond formation in Diels–Alder reactions

inferredcites →https://doi.org/10.1073/pnas.231313098openalex-snapshot

Structure of trichodiene synthase from Fusarium sporotrichioides provides mechanistic inferences on the terpene cyclization cascade

inferredcites →https://doi.org/10.1073/pnas.37.11.729openalex-snapshot

Configurations of Polypeptide Chains With Favored Orientations Around Single Bonds

inferredcites →https://doi.org/10.1103/physrevb.37.785openalex-snapshot

Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density

inferredcites →https://doi.org/10.1104/pp.105.059386openalex-snapshot

Surrogate Splicing for Functional Analysis of Sesquiterpene Synthase Genes

inferredcites →https://doi.org/10.1105/tpc.019877openalex-snapshot

The Variability of Sesquiterpenes Emitted from Two Zea mays Cultivars Is Controlled by Allelic Variation of Two Terpene Synthase Genes Encoding Stereoselective Multiple Product Enzymes

inferredcites →https://doi.org/10.1110/ps.072963707openalex-snapshot

How similar are enzyme active site geometries derived from quantum mechanical theozymes to crystal structures of enzyme‐inhibitor complexes? Implications for enzyme design

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02417.xopenalex-snapshot

Two sesquiterpene synthases are responsible for the complex mixture of sesquiterpenes emitted from Arabidopsis flowers

inferredcites →https://doi.org/10.1126/science.271.5246.163openalex-snapshot

Cation-π Interactions in Chemistry and Biology: A New View of Benzene, Phe, Tyr, and Trp

inferredcites →https://doi.org/10.1128/aem.61.11.3815-3820.1995openalex-snapshot

Production of volatile sesquiterpenes by Fusarium sambucinum strains with different abilities to synthesize trichothecenes

inferredcites →https://doi.org/10.1146/annurev.physchem.48.1.511openalex-snapshot

“STRONG” HYDROGEN BONDS IN CHEMISTRY AND BIOLOGY

inferredcites →https://doi.org/10.1201/9781003069232openalex-snapshot

Concerted Organic and Bio-organic Mechanisms

inferredcites →https://doi.org/10.1246/bcsj.55.1561openalex-snapshot

Six New Sesquiterpenoids from the Red Alga Laurencia nipponica Yamada

inferredcites →https://doi.org/10.1351/pac-con-12-11-22openalex-snapshot

Inherent dynamical preferences in carbocation rearrangements leading to terpene natural products

inferredcites →https://doi.org/10.1351/pac-con-13-01-03openalex-snapshot

Hyperconjugation in hydrocarbons: Not just a “mild sort of conjugation”

inferredcites →https://doi.org/10.3762/bjoc.9.37openalex-snapshot

Caryolene-forming carbocation rearrangements

What points at this work

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

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Identification and characterization of (+)-α-bisabolol and 7-epi-silphiperfol-5-ene synthases from Artemisia abrotanum

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A Bioinspired Catalytic Oxygenase Cascade to Generate Complex Oxindoles

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Bedeutung der inhärenten Substratreaktivität bei enzymvermittelten Cyclisierungen/Umlagerungen von Carbokationen

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A Bioinspired Catalytic Oxygenase Cascade to Generate Complex Oxindoles

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Importance of Inherent Substrate Reactivity in Enzyme‐Promoted Carbocation Cyclization/Rearrangements

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Designed Water Capture in Terpene Synthase Catalysis

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Specific and Multi‐Product Clade I and Clade IV Sesquiterpene Synthases Contribute to the Psilocybe cubensis Volatilome

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Using Terpene Synthase Plasticity in Catalysis: On the Enzymatic Conversion of Synthetic Farnesyl Diphosphate Analogues

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Concertedness and Activation Energy Control by Distal Methyl Group during Ring Contraction/Expansion in Scalarane‐Type Sesterterpenoid Biosynthesis

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Optimizing Amine‐Mediated Alkyne–Allene Isomerization to Improve Benzannulation Cascades: Synergy between Theory and Experiments

inferred← citeshttps://doi.org/10.1002/rcm.7411openalex-snapshot

Electrospray ionization tandem mass spectrometry analysis of isopimarane diterpenes from Velloziaceae

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Investigation of fragmentation pathways of norpimarane diterpenoids by mass spectrometry combined with computational chemistry

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Identification of new PTP1B-inhibiting decipiene diterpenoid esters from Eremophila clarkei by high-resolution PTP1B inhibition profiling, enzyme kinetics analysis, and molecular docking

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Peak-bridges due to in-column analyte transformations as a new tool for establishing molecular connectivities by comprehensive two-dimensional gas chromatography–mass spectrometry

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Enzymatic control of product distribution in terpene synthases: insights from multiscale simulations

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Latent potentials of the white-rot basidiomycete Phanerochaete chrysosporium responsible for sesquiterpene metabolism: CYP5158A1 and CYP5144C8 decorate (E)-α-bisabolene

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Predicting functions of putative fungal sesquiterpene synthase genes based on multiomics data analysis

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Early detection of dry bubble disease in Agaricus bisporus using volatile compounds

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A pivotal switch in β-domain determines the substrate selectivity of terpene synthases involved in Gardenia jasminoides floral scent synthesis

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Computationally aided stereochemical assignment of undescribed bisabolenes from Calea urticifolia

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Eremane, viscidane and isozizaene diterpenoids from the leaves of Eremophila rigida and their absolute configurations

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Gregarithecinol, a trichodiene/bazzanene derivative from Gregarithecium curvisporum KT4079: DFT-supported stereochemical elucidation of units linked by a rotatable bond

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Structural and Chemical Biology of Terpenoid Cyclases

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Functional Characterization of a Sesquiterpene Synthase Involved in Stereospecific Biosynthesis of β-Bisabolol

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RxnNet: An AI Framework for Reaction Mechanism Discovery─A Case Study of Carbocations

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Cyclopropylcarbinyl-to-Homoallyl Carbocation Equilibria Influence the Stereospecificity in the Nucleophilic Substitution of Cyclopropylcarbinols

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Substituent Effects on the Equilibria between Cyclopropylcarbinyl, Bicyclobutonium, Homoallyl, and Cyclobutyl Cations

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Scholl Cyclizations of Aryl Naphthalenes: Rearrangement Precedes Cyclization

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Carbanion Translocations via Intramolecular Proton Transfers: A Quantum Chemical Study

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Tension between Internal and External Modes of Stabilization in Carbocations Relevant to Terpene Biosynthesis: Modulating Minima Depth via C–H···π Interactions

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Artaboterpenoids A and B, Bisabolene-Derived Sesquiterpenoids from Artabotrys hexapetalus

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Active Site Loop Engineering Abolishes Water Capture in Hydroxylating Sesquiterpene Synthases

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Comment on “Substrate Folding Modes in Trichodiene Synthase: A Determinant of Chemo- and Stereoselectivity”

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Identification and Functional Characterization of UbiA-Type Terpene Synthases in Inonotus obliquus

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Feasibility of Intramolecular Proton Transfers in Terpene Biosynthesis – Guiding Principles

inferred← citeshttps://doi.org/10.1021/ja512901aopenalex-snapshot

Bicyclobutonium Ions in Biosynthesis – Interconversion of Cyclopropyl-Containing Sterols from Orchids

inferred← citeshttps://doi.org/10.1021/jacs.0c06295openalex-snapshot

Solvation Dynamics and the Nature of Reaction Barriers and Ion-Pair Intermediates in Carbocation Reactions

inferred← citeshttps://doi.org/10.1021/jacs.0c11348openalex-snapshot

The Impression of a Nonexisting Catalytic Effect: The Role of CotB2 in Guiding the Complex Biosynthesis of Cyclooctat-9-en-7-ol

inferred← citeshttps://doi.org/10.1021/jacs.4c14486openalex-snapshot

Assembly of Pyrenes through a Quadruple Photochemical Cascade: Blocking Groups Allow Diversion from the Double Mallory Path to Photocyclization at the Bay Region

inferred← citeshttps://doi.org/10.1021/jacs.4c17818openalex-snapshot

Characterization and Engineering of a Bisabolene Synthase Reveal an Unusual Hydride Shift and Key Residues Critical for Mono-, Bi-, and Tricyclic Sesquiterpenes Formation

inferred← citeshttps://doi.org/10.1021/jacs.6b07328openalex-snapshot

Dynamics and the Regiochemistry of Nitration of Toluene

inferred← citeshttps://doi.org/10.1021/jacs.6c13500openalex-snapshot

Discovery and Mechanistic Investigation of a Bacteria-Derived Sesquiterpene Ether Synthase AceS Catalyzing Syn -Protoetherification

inferred← citeshttps://doi.org/10.1021/jacsau.3c00039openalex-snapshot

Revision of the Peniroquesine Biosynthetic Pathway by Retro-Biosynthetic Theoretical Analysis: Ring Strain Controls the Unique Carbocation Rearrangement Cascade

inferred← citeshttps://doi.org/10.1021/np500819fopenalex-snapshot

Mechanistic Studies on the Autoxidation of α-Guaiene: Structural Diversity of the Sesquiterpenoid Downstream Products

inferred← citeshttps://doi.org/10.1038/s41929-022-00735-0openalex-snapshot

Catalytic role of carbonyl oxygens and water in selinadiene synthase

inferred← citeshttps://doi.org/10.1039/c3cs60452gopenalex-snapshot

How cyclobutanes are assembled in nature – insights from quantum chemistry

inferred← citeshttps://doi.org/10.1039/c3sc53293copenalex-snapshot

Predicting pathways for terpene formation from first principles – routes to known and new sesquiterpenes

inferred← citeshttps://doi.org/10.1039/c4sc03782kopenalex-snapshot

Modulation of inherent dynamical tendencies of the bisabolyl cation via preorganization in epi-isozizaene synthase

inferred← citeshttps://doi.org/10.1039/c5ob00169bopenalex-snapshot

Design and synthesis of analogues of natural products

inferred← citeshttps://doi.org/10.1039/c5sc02056eopenalex-snapshot

Biosynthetic insights provided by unusual sesterterpenes from the medicinal herb Aletris farinosa

inferred← citeshttps://doi.org/10.1039/c7ob01628jopenalex-snapshot

Sigmatropic proton shifts: a quantum chemical study

inferred← citeshttps://doi.org/10.1039/c7ob02463kopenalex-snapshot

Substituent effects on stereoselectivity of dihalocarbene reactions with cyclohexadiene and on the reactivity of bis-dihalocyclopropanes in electrophilic nitrations en route to pyrimidine N -oxides

inferred← citeshttps://doi.org/10.1039/c8cc01744aopenalex-snapshot

The absolute configuration of isochamigrene: new insights into the cyclisation mechanism of trichodiene synthase

inferred← citeshttps://doi.org/10.1039/c8sc03567aopenalex-snapshot

Pushing the limits of concertedness. A waltz of wandering carbocations

inferred← citeshttps://doi.org/10.1039/c9cc07681fopenalex-snapshot

Characterisation of three terpene synthases for β-barbatene, β-araneosene and nephthenol from social amoebae

inferred← citeshttps://doi.org/10.1039/d5cb00213copenalex-snapshot

Biosynthesis of sydonol reveals a new bisabolene cyclase and an unusual P450 aromatase

inferred← citeshttps://doi.org/10.1073/pnas.1505127112openalex-snapshot

Computational-guided discovery and characterization of a sesquiterpene synthase from Streptomyces clavuligerus

inferred← citeshttps://doi.org/10.1093/bib/bbac197openalex-snapshot

Bio-inspired chemical space exploration of terpenoids

inferred← citeshttps://doi.org/10.1111/1541-4337.12516openalex-snapshot

Sesquiterpenes in grapes and wines: Occurrence, biosynthesis, functionality, and influence of winemaking processes

inferred← citeshttps://doi.org/10.1111/tpj.70575openalex-snapshot

A multifunctional sesquiterpene synthase integrates with cytochrome P450s to reinforce the terpenoid defense network in maize

inferred← citeshttps://doi.org/10.1134/s1063784220080113openalex-snapshot

Analysis of Electrostatic Interaction between Dimer Complexes. Part II: Criteria and Conditions on Inhibitors of APP Protein Derivatives

inferred← citeshttps://doi.org/10.1155/ijfo/5819069openalex-snapshot

Volatilome Profiling of Mycotoxigenic Fungi Aspergillus carbonarius and Penicillium verrucosum in Mono‐ and Coculture With Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1371/journal.pcbi.1003874openalex-snapshot

Predicting the Functions and Specificity of Triterpenoid Synthases: A Mechanism-Based Multi-intermediate Docking Approach

inferred← citeshttps://doi.org/10.3389/fgene.2020.00421openalex-snapshot

Comparative (Within Species) Genomics of the Vitis vinifera L. Terpene Synthase Family to Explore the Impact of Genotypic Variation Using Phased Diploid Genomes

inferred← citeshttps://doi.org/10.3389/fpls.2019.00177openalex-snapshot

Linking Terpene Synthases to Sesquiterpene Metabolism in Grapevine Flowers

inferred← citeshttps://doi.org/10.3389/fpls.2026.1833733openalex-snapshot

Integrated characterization of six sesquiterpene synthases unravels diversified terpene biosynthesis in the mint species Leucosceptrum canum

inferred← citeshttps://doi.org/10.3390/antibiotics12101558openalex-snapshot

Development and Validation of a Gas Chromatography–Mass Spectrometry Method for the Analysis of the Novel Plant-Based Substance with Antimicrobial Activity

inferred← citeshttps://doi.org/10.3390/bioengineering10030392openalex-snapshot

A Single Active-Site Mutagenesis Confers Enhanced Activity and/or Changed Product Distribution to a Pentalenene Synthase from Streptomyces sp. PSKA01

inferred← citeshttps://doi.org/10.3390/jof10050350openalex-snapshot

Genome Mining of Fungal Unique Trichodiene Synthase-like Sesquiterpene Synthases

inferred← citeshttps://doi.org/10.3390/jof9101017openalex-snapshot

Molecular and Functional Analyses of Characterized Sesquiterpene Synthases in Mushroom-Forming Fungi

inferred← citeshttps://doi.org/10.3390/md18080426openalex-snapshot

Secondary Metabolites with Nitric Oxide Inhibition from Marine-Derived Fungus Alternaria sp. 5102

inferred← citeshttps://doi.org/10.3390/md24020061openalex-snapshot

Smart Secondary Metabolites in Marine Environments: The Case of Elatol

inferred← citeshttps://doi.org/10.3390/md24090316openalex-snapshot

Macrocarpane-Type Sesquiterpenes from Laurencia microcladia

inferred← citeshttps://doi.org/10.3390/molecules23061353openalex-snapshot

Chemotypes and Biomarkers of Seven Species of New Caledonian Liverworts from the Bazzanioideae Subfamily

inferred← citeshttps://doi.org/10.3762/bjoc.18.97openalex-snapshot

Understanding the competing pathways leading to hydropyrene and isoelisabethatriene

inferred← citeshttps://doi.org/10.70675/e96a25b2ze920z41edz9026zcb1d858b1cd1openalex-snapshot

Contribution à l'étude de la chimiodiversité des hépatiques de Nouvelle-Calédonie

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