On the public citation graph
Total Synthesis of Hyperforin
0 signed · 171 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/adsc.201400085openalex-snapshot
Copper‐Catalysed Conjugate Addition of Grignard Reagents to 2‐Methylcyclopentenone and Sequential Enolate Alkylation
inferredcites →https://doi.org/10.1002/anie.200500776openalex-snapshot
Construction of Highly Functionalized Medium‐Sized Rings: Synthesis of Hyperforin and Perforatumone Model Systems
inferredcites →https://doi.org/10.1002/anie.200605207openalex-snapshot
Phloroglucinol Derivatives Guttiferone G, Aristoforin, and Hyperforin: Inhibitors of Human Sirtuins SIRT1 and SIRT2
inferredcites →https://doi.org/10.1002/anie.200703886openalex-snapshot
Differentiation of Nonconventional “Carbanions”—The Total Synthesis of Nemorosone and Clusianone
inferredcites →https://doi.org/10.1002/anie.200906678openalex-snapshot
Catalytic Asymmetric Total Synthesis of ent‐Hyperforin
inferredcites →https://doi.org/10.1002/anie.201005183openalex-snapshot
Catalytic Enantioselective Claisen Rearrangements of O‐Allyl β‐Ketoesters
inferredcites →https://doi.org/10.1002/anie.201103873openalex-snapshot
The Chemistry of the Polycyclic Polyprenylated Acylphloroglucinols
inferredcites →https://doi.org/10.1002/anie.201306256openalex-snapshot
The Bidirectional Total Synthesis of Sampsonione P and Hyperibone I
inferredcites →https://doi.org/10.1002/anie.201403939openalex-snapshot
Total Syntheses of Hyperforin and Papuaforins A–C, and Formal Synthesis of Nemorosone through a Gold(I)‐Catalyzed Carbocyclization
inferredcites →https://doi.org/10.1002/anie.201404437openalex-snapshot
Asymmetric, Stereodivergent Synthesis of (−)‐Clusianone Utilizing a Biomimetic Cationic Cyclization
inferredcites →https://doi.org/10.1002/ejoc.200700430openalex-snapshot
Synthetic Studies Towards Bridgehead Diprenyl‐Substituted Bicyclo[3.3.1]nonane‐2,9‐diones as Models for Polyprenylated Acylphloroglucinol Construction
inferredcites →https://doi.org/10.1002/ejoc.201101629openalex-snapshot
A Chiral‐Pool‐Based Approach to the Core Structure of (+)‐Hyperforin
inferredcites →https://doi.org/10.1002/ejoc.201300815openalex-snapshot
Chemistry and Biology of the Polycyclic Polyprenylated Acylphloroglucinol Hyperforin
inferredcites →https://doi.org/10.1016/j.bmcl.2011.02.074openalex-snapshot
Asymmetric total synthesis of (+)- and (−)-clusianone and (+)- and (−)-clusianone methyl enol ether via ACC alkylation and evaluation of their anti-HIV activity
inferredcites →https://doi.org/10.1016/j.tet.2003.03.001openalex-snapshot
Synthesis of a model system for the preparation of phloroglucinol containing natural products
inferredcites →https://doi.org/10.1016/j.tet.2010.05.086openalex-snapshot
The first catalytic asymmetric total synthesis of ent-hyperforin
inferredcites →https://doi.org/10.1016/j.tet.2011.06.079openalex-snapshot
Synthetic efforts toward [3.3.1] bridged bicyclic phloroglucinol natural products
inferredcites →https://doi.org/10.1016/j.tet.2012.12.066openalex-snapshot
An approach toward the synthesis of PPAP natural product garsubellin A: construction of the tricyclic core
inferredcites →https://doi.org/10.1016/j.tetlet.2003.12.023openalex-snapshot
Towards an enantiospecific total synthesis of garsubellin A and related phloroglucin natural products: the α-pinene approach
inferredcites →https://doi.org/10.1016/j.tetlet.2004.08.068openalex-snapshot
Construction of the bicyclo[3.3.1]nonenone core by successive Michael reactions of 2-cyclohexenone derivatives
inferredcites →https://doi.org/10.1016/j.tetlet.2005.11.120openalex-snapshot
A rapid acquisition of the bicyclo[3.3.1]nonan-9-one core present in garsubellin A and related phloroglucins
inferredcites →https://doi.org/10.1016/j.tetlet.2007.04.080openalex-snapshot
A new approach for the construction of a highly congested bicyclic system in polycyclic polyprenylated acylphloroglucinols (PPAPs)
inferredcites →https://doi.org/10.1016/j.tetlet.2007.11.069openalex-snapshot
Progress towards the synthesis of papuaforin A: selective formation of α-bromoenones from silyl enol ethers
inferredcites →https://doi.org/10.1016/j.tetlet.2007.12.063openalex-snapshot
A stereodefined approach towards the bicyclo[3.3.1]nonan-9-one core of the phloroglucin natural products guttiferone A and hypersampsone F
inferredcites →https://doi.org/10.1016/j.tetlet.2007.12.065openalex-snapshot
A concise approach towards the bicyclo[3.3.1]nonan-9-one core present in the phloroglucin natural product hyperforin
inferredcites →https://doi.org/10.1016/j.tetlet.2009.03.041openalex-snapshot
Synthetic studies towards the phloroglucin natural product hyperforin: construction of the fully prenylated bicyclic core
inferredcites →https://doi.org/10.1016/j.tetlet.2009.12.147openalex-snapshot
Synthetic studies on nemorosone via enantioselective intramolecular cyclopropanation
inferredcites →https://doi.org/10.1016/j.tetlet.2012.06.045openalex-snapshot
Synthetic studies toward geranylated PPAP natural products oblongifolin A, oblongifolin D, and enervosanone
inferredcites →https://doi.org/10.1016/j.tetlet.2013.02.021openalex-snapshot
Stereoselective total synthesis of (±)-hyperforin via intramolecular cyclopropanation
inferredcites →https://doi.org/10.1016/s0040-4039(00)75241-5openalex-snapshot
The structure of hyperforin
inferredcites →https://doi.org/10.1016/s0040-4039(01)81503-3openalex-snapshot
A favorski reaction using iodosobenzene
inferredcites →https://doi.org/10.1016/s0040-4039(01)81706-8openalex-snapshot
Steric effects in the hypervalent iodine oxidation of ketones
inferredcites →https://doi.org/10.1016/s0040-4039(02)00650-0openalex-snapshot
Studies toward the total synthesis of garsubellin A: synthesis of 8-deprenyl-garsubellin A
inferredcites →https://doi.org/10.1016/s0040-4039(02)02693-xopenalex-snapshot
Synthesis of the core bicyclic system of hyperforin and nemorosone
inferredcites →https://doi.org/10.1016/s0040-4039(03)01023-2openalex-snapshot
New cascade reactions starting from acetylenic ω-ketoesters: an easy access to electrophilic allenes and to 1,3-bridgehead ketones
inferredcites →https://doi.org/10.1021/acs.orglett.5b01121openalex-snapshot
Total Synthesis of (−)-Nemorosone and (+)-Secohyperforin
inferredcites →https://doi.org/10.1021/bi0268753openalex-snapshot
2.1 Å Crystal Structure of Human PXR in Complex with the St. John's Wort Compound Hyperforin,
inferredcites →https://doi.org/10.1021/cr0500582openalex-snapshot
Polycyclic Polyprenylated Acylphloroglucinols
inferredcites →https://doi.org/10.1021/ja055301topenalex-snapshot
Total Synthesis of (±)-Garsubellin A
inferredcites →https://doi.org/10.1021/ja0762339openalex-snapshot
Rapid Access to Polyprenylated Phloroglucinols via Alkylative Dearomatization−Annulation: Total Synthesis of (±)-Clusianone
inferredcites →https://doi.org/10.1021/ja1057828openalex-snapshot
Catalytic Enantioselective Alkylative Dearomatization−Annulation: Total Synthesis and Absolute Configuration Assignment of Hyperibone K
inferredcites →https://doi.org/10.1021/ja312150dopenalex-snapshot
Enantioselective Total Synthesis of Hyperforin
inferredcites →https://doi.org/10.1021/ja500063aopenalex-snapshot
The Total Syntheses of Guttiferone A and 6-epi-Guttiferone A
inferredcites →https://doi.org/10.1021/ja9905445openalex-snapshot
Synthesis of the Fully Functionalized Bicyclic Core of Garsubellin A
inferredcites →https://doi.org/10.1021/jm0209782openalex-snapshot
Biosynthesis of Hyperforin in Hypericum perforatum
inferredcites →https://doi.org/10.1021/jo00103a042openalex-snapshot
Conjugate Addition Reactions of Allylic Copper Species Derived from Grignard Reagents: Synthetic and Spectroscopic Aspects
inferredcites →https://doi.org/10.1021/jo010884kopenalex-snapshot
A Preliminary Approach to Nonenolizable β,β-Tricarbonyls: Assembly of a Hyperevolutin Prototype1
inferredcites →https://doi.org/10.1021/jo061820iopenalex-snapshot
Direct Cyanation of Heteroaromatic Compounds Mediated by Hypervalent Iodine(III) Reagents: In Situ Generation of PhI(III)−CN Species and Their Cyano Transfer
inferredcites →https://doi.org/10.1021/jo070388hopenalex-snapshot
Synthesis of Polyprenylated Acylphloroglucinols Using Bridgehead Lithiation: The Total Synthesis of Racemic Clusianone and a Formal Synthesis of Racemic Garsubellin A
inferredcites →https://doi.org/10.1021/jo300646jopenalex-snapshot
Stereoselective Total Synthesis of Nemorosone
inferredcites →https://doi.org/10.1021/jo500027kopenalex-snapshot
Biomimetic Total Synthesis of (±)-Doitunggarcinone A and (+)-Garcibracteatone
inferredcites →https://doi.org/10.1021/jo5026699openalex-snapshot
Enantioselective Approach to Polycyclic Polyprenylated Acylphloroglucinols via Catalytic Asymmetric Intramolecular Cyclopropanation
inferredcites →https://doi.org/10.1021/ol0255965openalex-snapshot
Studies toward the Total Synthesis of Garsubellin A: A Concise Synthesis of the 18-epi-Tricyclic Core
inferredcites →https://doi.org/10.1021/ol025968+openalex-snapshot
Progress toward the Synthesis of Garsubellin A and Related Phloroglucins: The Direct Diastereoselective Synthesis of the Bicyclo[3.3.1]nonane Core
inferredcites →https://doi.org/10.1021/ol0357907openalex-snapshot
A New Synthetic Approach to the Polycyclic Polyprenylated Acylphloroglucinols
inferredcites →https://doi.org/10.1021/ol0620592openalex-snapshot
Synthesis of (+/−)-Clusianone: High-Yielding Bridgehead and Diketone Substitutions by Regioselective Lithiation of Enol Ether Derivatives of Bicyclo[3.3.1]nonane-2,4,9-triones
inferredcites →https://doi.org/10.1021/ol062736sopenalex-snapshot
α,α‘-Annulation of 2,6-Prenyl-Substituted Cyclohexanone Derivatives with Malonyl Chloride: Application to a Short Synthesis of (±)-Clusianone. Formation and Rearrangement of a Biogenetic-Like Intermediate
inferredcites →https://doi.org/10.1021/ol101380aopenalex-snapshot
Biomimetic Synthesis of Polycyclic Polyprenylated Acylphloroglucinol Natural Products Isolated from Hypericum papuanum
inferredcites →https://doi.org/10.1021/ol1022728openalex-snapshot
Development of a Strategy for the Asymmetric Synthesis of Polycyclic Polyprenylated Acylphloroglucinols via N-Amino Cyclic Carbamate Hydrazones: Application to the Total Synthesis of (+)-Clusianone
inferredcites →https://doi.org/10.1021/ol300386topenalex-snapshot
Total Synthesis of (±)-7-epi-Nemorosone
inferredcites →https://doi.org/10.1021/ol302524qopenalex-snapshot
Biomimetic Total Synthesis of (±)-Garcibracteatone
inferredcites →https://doi.org/10.1021/ol4020909openalex-snapshot
An Unusual Michael-Induced Skeletal Rearrangement of a Bicyclo[3.3.1]nonane Framework of Phloroglucinols to a Novel Bioactive Bicyclo[3.3.0]octane
inferredcites →https://doi.org/10.1021/ol900590topenalex-snapshot
Manganese(III)-Mediated Transformations of Phloroglucinols: A Formal Oxidative [4 + 2] Cycloaddition Leading to Bicyclo[2.2.2]octadiones
inferredcites →https://doi.org/10.1021/ol901722qopenalex-snapshot
Gold-Catalyzed Synthesis of Carbon-Bridged Medium-Sized Rings
inferredcites →https://doi.org/10.1021/ol901781nopenalex-snapshot
A Short Biomimetic Approach to the Fully Functionalized Bicyclic Framework of Type A Acylphloroglucinols
inferredcites →https://doi.org/10.1021/ol990791dopenalex-snapshot
A Facile Method for the Solution and Solid-Phase Synthesis of Substituted [3.3.1] Bicycles
inferredcites →https://doi.org/10.1038/ja.2012.125openalex-snapshot
Stereoselective total synthesis of garsubellin A
inferredcites →https://doi.org/10.1038/nchem.1170openalex-snapshot
The total synthesis of hyperpapuanone, hyperibone L, epi-clusianone and oblongifolin A
inferredcites →https://doi.org/10.1039/b914364popenalex-snapshot
Phloroglucinol compounds of natural origin: Synthetic aspects
inferredcites →https://doi.org/10.1039/c0cc01419bopenalex-snapshot
An efficient oxidative dearomatization–radical cyclization approach to symmetrically substituted bicyclic guttiferone natural products
inferredcites →https://doi.org/10.1039/c2cc37914gopenalex-snapshot
Adventures in bridgehead substitution chemistry: synthesis of polycyclic polyprenylated acylphloroglucinols (PPAPs)
inferredcites →https://doi.org/10.1055/s-0029-1219371openalex-snapshot
Synthesis of Nemorosone via a Difficult Bridgehead Substitution Reaction
inferredcites →https://doi.org/10.1055/s-1976-24200openalex-snapshot
The Robinson Annelation and Related Reactions
inferredcites →https://doi.org/10.1073/pnas.130155097openalex-snapshot
St. John's wort induces hepatic drug metabolism through activation of the pregnane X receptor
inferredcites →https://doi.org/10.1096/fj.07-8110comopenalex-snapshot
Hyperforin—a key constituent of St. John's wort specifically activates TRPC6 channels
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113526zenodo-depositor-declared
Hyperforin: A natural lead compound with multiple pharmacological activities
inferred← citeshttps://doi.org/10.1002/047084289x.ri085.pub3openalex-snapshot
Isopropylmagnesium Bromide
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0953openalex-snapshot
Rearrangements and Fragmentations Mediated by Hypervalent Iodine Reagents
inferred← citeshttps://doi.org/10.1002/9783527699087.ch8openalex-snapshot
Novel Substrates and Nucleophiles in Asymmetric Copper‐Catalyzed Conjugate Addition Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201901263openalex-snapshot
Gold Catalyzed Cyclopropanation/[5+3] Cycloaddition of 1,4,9‐ and 1,4,10‐Allenenynes to Bicyclo[3.3.1]nonane Derivatives
inferred← citeshttps://doi.org/10.1002/ange.201507549openalex-snapshot
Strategien für die Synthese von Naturstoffen mit benachbarten stereogenen quartären Kohlenstoffatomen
inferred← citeshttps://doi.org/10.1002/ange.202010338openalex-snapshot
Synthesis and Multiplexed Activity Profiling of Synthetic Acylphloroglucinol Scaffolds
inferred← citeshttps://doi.org/10.1002/ange.202116136openalex-snapshot
Enantioselective Total Synthesis of Hyperforin and Pyrohyperforin
inferred← citeshttps://doi.org/10.1002/ange.202117480openalex-snapshot
Enantioselective Synthesis of (−)‐10‐Hydroxyacutuminine
inferred← citeshttps://doi.org/10.1002/ange.202200420openalex-snapshot
Bioinspired Total Synthesis of Erectones A and B, and the Revised Structure of Hyperelodione D
inferred← citeshttps://doi.org/10.1002/ange.202203311openalex-snapshot
Intramolecular Tricarbonyl‐Ene Reactions and α‐Hydroxy‐β‐Diketone Rearrangements Inspired by the Biosynthesis of Polycyclic Polyprenylated Acylphloroglucinols
inferred← citeshttps://doi.org/10.1002/ange.202501008openalex-snapshot
Divergent Total Syntheses of Six Crinipellin‐Type Diterpenoids through Tandem 4π‐Electrocyclization/Dicycloexpansion
inferred← citeshttps://doi.org/10.1002/anie.201507549openalex-snapshot
Synthetic Strategies toward Natural Products Containing Contiguous Stereogenic Quaternary Carbon Atoms
inferred← citeshttps://doi.org/10.1002/anie.202010338openalex-snapshot
Synthesis and Multiplexed Activity Profiling of Synthetic Acylphloroglucinol Scaffolds
inferred← citeshttps://doi.org/10.1002/anie.202116136openalex-snapshot
Enantioselective Total Synthesis of Hyperforin and Pyrohyperforin
inferred← citeshttps://doi.org/10.1002/anie.202117480openalex-snapshot
Enantioselective Synthesis of (−)‐10‐Hydroxyacutuminine
inferred← citeshttps://doi.org/10.1002/anie.202200420openalex-snapshot
Bioinspired Total Synthesis of Erectones A and B, and the Revised Structure of Hyperelodione D
inferred← citeshttps://doi.org/10.1002/anie.202203311openalex-snapshot
Intramolecular Tricarbonyl‐Ene Reactions and α‐Hydroxy‐β‐Diketone Rearrangements Inspired by the Biosynthesis of Polycyclic Polyprenylated Acylphloroglucinols
inferred← citeshttps://doi.org/10.1002/anie.202501008openalex-snapshot
Divergent Total Syntheses of Six Crinipellin‐Type Diterpenoids through Tandem 4π‐Electrocyclization/Dicycloexpansion
inferred← citeshttps://doi.org/10.1002/chem.202202383openalex-snapshot
Evolution of a Synthetic Strategy for Garsubellin A
inferred← citeshttps://doi.org/10.1002/chem.202501269openalex-snapshot
Asymmetric 1,4‐Addition and Functionalization Strategy in Total Synthesis
inferred← citeshttps://doi.org/10.1002/cjoc.202100210openalex-snapshot
Hypermonones A—I, New Polyprenylated Acylphloroglucinols from Hypericum monogynum with Multidrug Resistance Reversal Activity
inferred← citeshttps://doi.org/10.1002/cjoc.202400739openalex-snapshot
Hyperkouytones A—O, New Polyprenylated Acylphloroglucinols from Hypericum kouytchense with Multidrug Resistance Reversal Activity
inferred← citeshttps://doi.org/10.1002/hlca.201900223openalex-snapshot
Asymmetric Synthesis of 2,3‐Disubstituted Cyclic Ketones by Enantioselective Conjugate Radical Additions
inferred← citeshttps://doi.org/10.1007/978-3-030-52966-6_2openalex-snapshot
The Phytochemistry and Pharmacology of Hypericum
inferred← citeshttps://doi.org/10.1007/978-3-031-42422-9_1openalex-snapshot
Neurotrophic Natural Products
inferred← citeshttps://doi.org/10.1007/s43450-022-00248-8openalex-snapshot
Pharmacological Profile of Garcinielliptone FC from Platonia insignis
inferred← citeshttps://doi.org/10.1016/b978-0-12-809593-5.00012-4openalex-snapshot
Biosynthetic and Total Synthetic Approaches for (+)-Hyperforin
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/j.bioorg.2021.105144openalex-snapshot
Polycyclic polyprenylated acylphloroglucinols with immunosuppressive activity from Hypericum perforatum and absolute configurations assignment of previously reported analogues
inferred← citeshttps://doi.org/10.1016/j.ejpb.2017.03.024openalex-snapshot
Biotechnological production of hyperforin for pharmaceutical formulation
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2016.02.016openalex-snapshot
Hyperforin production in Hypericum perforatum root cultures
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114047openalex-snapshot
Hyperatins A–D, highly oxidized polycyclic polyprenylated acylphloroglucinols from Hypericum perforatum L. with hypoglycemic potential in liver cells
inferred← citeshttps://doi.org/10.1016/j.tet.2016.07.030openalex-snapshot
Stereoselective construction of all-carbon quaternary stereocenters by allylboration of chiral aldehydes: synthesis of a fragment of (+)-vibsanin A
inferred← citeshttps://doi.org/10.1016/j.tet.2019.04.076openalex-snapshot
Catalytic enantioselective conjugate addition en route to paxilline indoloterpenoids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.11.041openalex-snapshot
Progress on PPAPs cyclization: Guttiferone A as a case study
inferred← citeshttps://doi.org/10.1021/acs.accounts.0c00055openalex-snapshot
Syntheses of Complex Terpenes from Simple Polyprenyl Precursors
inferred← citeshttps://doi.org/10.1021/acs.accounts.0c00781openalex-snapshot
Annulative Methods in the Synthesis of Complex Meroterpene Natural Products
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00551openalex-snapshot
Research Progress of Polycyclic Polyprenylated Acylphloroglucinols
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b01178openalex-snapshot
Tricyclic Polyprenylated Acylphloroglucinols from St John’s Wort, Hypericum perforatum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00763openalex-snapshot
Total Synthesis of Norsampsones A and B, Garcinielliptones N and O, and Hyperscabrin A
inferred← citeshttps://doi.org/10.1021/acs.joc.6b03043openalex-snapshot
Constructing 24(23→22)- abeo -Cholestane from Tigogenin in a 20(22→23)- abeo -Way via a PhI(OAc) 2 -mediated Favorskii Rearrangement
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00426openalex-snapshot
Modular Total Syntheses of Hyperforin, Papuaforins A, B, and C via Gold(I)-Catalyzed Carbocyclization
inferred← citeshttps://doi.org/10.1021/acs.oprd.8b00434openalex-snapshot
Automated On-Demand Titration of Organometallic Reagents in Continuous Flow
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02842openalex-snapshot
Pd-Catalyzed Enantioselective Dearomative Allylic Annulation to Access PPAPs Analogues
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01745openalex-snapshot
Total Synthesis of a PPAP, Nemorosonol, Using a Tandem Michael Addition–Intramolecular Aldol Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02232openalex-snapshot
Bioinspired Total Synthesis of Hyperireflexolides A and B
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01836openalex-snapshot
The Total Synthesis of Hyperfirin via a Cyclooctadiene Strategy
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02930openalex-snapshot
Asymmetric Total Synthesis of (+)-Hyperbeanol A
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04135openalex-snapshot
Isolation and Biomimetic Semisynthesis of Hyperzrones A and B, Two Nor-Polycyclic Polyprenylated Acylphloroglucinols with a Characteristic Cyclobutane Moiety, from Hypericum beanii
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00243openalex-snapshot
Transannular Acylation Facilitates C5–C9 Bond Formation in Hyperforin Total Synthesis
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00672openalex-snapshot
Access to Diverse Oxygen Heterocycles via Oxidative Rearrangement of Benzylic Tertiary Alcohols
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03078openalex-snapshot
Me2AlSEt-Promoted Domino Dieckmann Cyclization Enables the Total Synthesis of Polycyclic Polyprenylated Acylphloroglucinols
inferred← citeshttps://doi.org/10.1021/jacs.2c02627openalex-snapshot
Taming Shapeshifting Anions: Total Synthesis of Ocellatusone C
inferred← citeshttps://doi.org/10.1021/jacs.3c03960openalex-snapshot
A Shapeshifting Roadmap for Polycyclic Skeletal Evolution
inferred← citeshttps://doi.org/10.1021/jacs.4c07007openalex-snapshot
Total Synthesis of Hypersampsone M
inferred← citeshttps://doi.org/10.1021/jacs.4c09555openalex-snapshot
Total Synthesis of the Hexacyclic Sesterterpenoid Niduterpenoid B via Structural Reorganization Strategy
inferred← citeshttps://doi.org/10.1021/jacs.4c16769openalex-snapshot
Photocatalyzed Epimerization of Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1021/jacs.5c17047openalex-snapshot
Total Synthesis of Aconicarmisulfonine A, a Sulfonated Diterpene Alkaloid
inferred← citeshttps://doi.org/10.1021/jacs.5c20001openalex-snapshot
Total Synthesis of (+)-Melicolone K Enabled by a Late-Stage Programmed C–H Functionalization
inferred← citeshttps://doi.org/10.1021/jacs.6b10397openalex-snapshot
Annulative Methods Enable a Total Synthesis of the Complex Meroterpene Berkeleyone A
inferred← citeshttps://doi.org/10.1021/jacs.9b00925openalex-snapshot
Facile Access to Bridged Ring Systems via Point-to-Planar Chirality Transfer: Unified Synthesis of Ten Cyclocitrinols
inferred← citeshttps://doi.org/10.1021/jacsau.6c00404openalex-snapshot
Total Syntheses of (+)-Hyperbeanols A–C, (+)-Hyperpatulol A, and (−)-Hypercohone G, as Well as Structure Revision of Hyperpatulol A, and Hyperbeanol B
inferred← citeshttps://doi.org/10.1038/ja.2016.30openalex-snapshot
The first total synthesis and the second- or third-generation approach
inferred← citeshttps://doi.org/10.1038/s41467-020-14354-5openalex-snapshot
Programmable meroterpene synthesis
inferred← citeshttps://doi.org/10.1038/s41557-024-01533-wopenalex-snapshot
Modular chemoenzymatic synthesis of ten fusicoccane diterpenoids
inferred← citeshttps://doi.org/10.1039/c6cs00935bopenalex-snapshot
Recent applications of the 1,2-carbon atom migration strategy in complex natural product total synthesis
inferred← citeshttps://doi.org/10.1039/c6ra08805hopenalex-snapshot
Polycyclic polyprenylated acylphloroglucinols: natural phosphodiesterase-4 inhibitors from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1039/c6sc00932hopenalex-snapshot
Enantioselective synthesis of Iboga alkaloids and vinblastine via rearrangements of quaternary ammoniums
inferred← citeshttps://doi.org/10.1039/c7np00065kopenalex-snapshot
Total synthesis of complex terpenoids employing radical cascade processes
inferred← citeshttps://doi.org/10.1039/c7ra05947gopenalex-snapshot
Norsampsone E, an unprecedented decarbonyl polycyclic polyprenylated acylphloroglucinol with a homoadamantyl core from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1039/c8ob02067aopenalex-snapshot
Bioactive polycyclic polyprenylated acylphloroglucinols from Hypericum perforatum
inferred← citeshttps://doi.org/10.1039/d0nj05078dopenalex-snapshot
Innovation of hypervalent( iii ) iodine in the synthesis of natural products
inferred← citeshttps://doi.org/10.1039/d0np00005aopenalex-snapshot
An invocation for computational evaluation of isomerization transforms: cationic skeletal reorganizations as a case study
inferred← citeshttps://doi.org/10.1039/d0ob02072aopenalex-snapshot
Two new seco-polycyclic polyprenylated acylphloroglucinol from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1039/d0sc03249bopenalex-snapshot
Catalytic enantioselective construction of vicinal quaternary carbon stereocenters
inferred← citeshttps://doi.org/10.1039/d1np00077bopenalex-snapshot
Recent advances in the synthesis of natural products containing the phloroglucinol motif
inferred← citeshttps://doi.org/10.1039/d1qo00282aopenalex-snapshot
Strategies towards endo -type B polycyclic polyprenylated acylphloroglucinols: total synthesis of regio -hyperibone L and (+)- epi -clusianone
inferred← citeshttps://doi.org/10.1039/d1sc02613eopenalex-snapshot
Chemical investigations into the biosynthesis of the gymnastatin and dankastatin alkaloids
inferred← citeshttps://doi.org/10.1039/d1sc03356eopenalex-snapshot
Unprecedented polycyclic polyprenylated acylphloroglucinols with anti-Alzheimer's activity from St. John's wort
inferred← citeshttps://doi.org/10.1039/d2np00042copenalex-snapshot
Dearomative logic in natural product total synthesis
inferred← citeshttps://doi.org/10.1039/d3cc01268aopenalex-snapshot
Total synthesis and structural reassignment of garcinielliptone FC, a polycyclic polyprenylated acylphloroglucinol with diverse bioactivity
inferred← citeshttps://doi.org/10.1039/d3np00066dopenalex-snapshot
Controllable skeletal reorganizations in natural product synthesis
inferred← citeshttps://doi.org/10.1039/d3ob01840gopenalex-snapshot
Sequential Dieckmann cyclization enables the total synthesis of 7- epi -clusianone and 18-hydroxy-7- epi -clusianone
inferred← citeshttps://doi.org/10.1039/d5qo01477hopenalex-snapshot
Recent advances in the total synthesis of polycyclic phloroglucinol natural products
inferred← citeshttps://doi.org/10.1055/a-2526-0619openalex-snapshot
Synthetic Studies of Polycyclic Polyprenylated Acylphloroglucinols: Asymmetric Construction of a Cyclohexanone Moiety
inferred← citeshttps://doi.org/10.1080/00304948.2018.1405332openalex-snapshot
Synthesis and Applications of Tricarbonylmethane Compounds
inferred← citeshttps://doi.org/10.1126/science.adr8612openalex-snapshot
Catalytic prenyl conjugate additions for synthesis of enantiomerically enriched PPAPs
inferred← citeshttps://doi.org/10.17344/acsi.2021.6921openalex-snapshot
Recent Chemical Methodology Advances in the Total Synthesis of Meroterpenoids
inferred← citeshttps://doi.org/10.2174/1567205017666200528162046openalex-snapshot
Reversal of Calcium Dysregulation as Potential Approach for Treating Alzheimer's Disease
inferred← citeshttps://doi.org/10.3390/cells9112351openalex-snapshot
Potential Drug Candidates to Treat TRPC6 Channel Deficiencies in the Pathophysiology of Alzheimer’s Disease and Brain Ischemia
inferred← citeshttps://doi.org/10.3987/com-18-s(f)31openalex-snapshot
Studies toward the Synthesis of Perforatumone: Synthesis of the 7-Oxabicyclo[4.2.1]nonane-8,9-dione Core
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.