On the public citation graph
Chemoenzymatic Synthesis of trans-Tetrahydrofuran Cores of Annonaceous Acetogenins from Bromobenzene
0 signed · 57 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known work and none has been retracted — and get a dated CiteStamped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/(sici)1099-0690(200001)2000:2<349::aid-ejoc349>3.0.co;2-jopenalex-snapshot
A Facile Route to Bulladecin-Type Acetogenins - Total Synthesis of Asimilobinand Correction of the Configuration of Its Tetrahydrofuran Segment
inferredcites →https://doi.org/10.1002/1099-0690(200103)2001:5<997::aid-ejoc997>3.0.co;2-7openalex-snapshot
Reactions of 1,5-Dienes with Ruthenium Tetraoxide: Stereoselective Synthesis of Tetrahydrofurandiols
inferredcites →https://doi.org/10.1002/1521-3765(20000703)6:13<2382::aid-chem2382>3.3.co;2-3openalex-snapshot
A Convergent Total Synthesis of (−)-Mucocin: An Acetogenin from Annonaceae
inferredcites →https://doi.org/10.1002/1521-3765(20020402)8:7<1621::aid-chem1621>3.0.co;2-8openalex-snapshot
The Total Synthesis of the Annonaceous Acetogenin, Muricatetrocin C
inferredcites →https://doi.org/10.1002/1521-3773(20001016)39:20<3622::aid-anie3622>3.0.co;2-hopenalex-snapshot
The Total Synthesis of the Annonaceous Acetogenin, Muricatetrocin C
inferredcites →https://doi.org/10.1002/cbic.200400396openalex-snapshot
Annonaceous Acetogenins: The Hydroxyl Groups and THF Rings Are Crucial Structural Elements for Targeting the Mitochondria, Demonstration with the Synthesis of Fluorescent Squamocin Analogues
inferredcites →https://doi.org/10.1016/0014-5793(94)80380-3openalex-snapshot
Mitochondrial respiratory chain inhibitors induce apoptosis
inferredcites →https://doi.org/10.1016/0040-4020(80)85026-5openalex-snapshot
Stereocontrol in the synthesis of acyclic systems: applications to natural product synthesis
inferredcites →https://doi.org/10.1016/0304-3835(82)90078-7openalex-snapshot
Thiol-dependent inhibition of RNA synthesis in vitro by acridines. Structure-inhibition relationships
inferredcites →https://doi.org/10.1016/j.bmc.2008.08.030openalex-snapshot
Synthesis and antitumor activity of C-9 epimers of the tetrahydrofuran containing acetogenin 4-deoxyannoreticuin
inferredcites →https://doi.org/10.1016/j.bmcl.2009.02.105openalex-snapshot
Structure–activity relationships of diverse annonaceous acetogenins against human tumor cells
inferredcites →https://doi.org/10.1016/j.tetasy.2005.02.012openalex-snapshot
Chemoenzymatic synthesis of enantiopure α-substituted cyclohexanones from aromatic compounds
inferredcites →https://doi.org/10.1016/s0040-4020(00)00878-4openalex-snapshot
A Modular Synthesis of the Bis-Tetrahydrofuran Core of Rolliniastatin from Pyranoside Precursors
inferredcites →https://doi.org/10.1016/s0040-4039(00)79027-7openalex-snapshot
Stereoselection in iodolactonisations of 3-silyloxy-5-alkenoic acids
inferredcites →https://doi.org/10.1016/s0040-4039(00)79028-9openalex-snapshot
Iodine-induced cyclisations of (E)- and (Z)-3-hydroxy-5-alkenoates: Stereoselective approaches to trisubstituted tetrahydrofurans
inferredcites →https://doi.org/10.1016/s0304-3835(97)04716-2openalex-snapshot
The Annonaceous acetogenin bullatacin is cytotoxic against multidrug-resistant human mammary adenocarcinoma cells
inferredcites →https://doi.org/10.1021/ar00057a001openalex-snapshot
Syntheses of Acetogenins of Annonaceae: A New Class of Bioactive Polyketides
inferredcites →https://doi.org/10.1021/bi972348lopenalex-snapshot
Membrane Conformations and Their Relation to Cytotoxicity of Asimicin and Its Analogues
inferredcites →https://doi.org/10.1021/ja00222a008openalex-snapshot
Homoallylic chiral induction in the synthesis of 2,4-disubstituted tetrahydrofurans by iodoetherification. Synthetic scope and chiral induction mechanism
inferredcites →https://doi.org/10.1021/ja00237a006openalex-snapshot
Modeling chemical reactivity. 7. The effect of a change in rate-limiting step on the stereoselectivity of electrophilic addition to allylic alcohols and related chiral alkenes
inferredcites →https://doi.org/10.1021/jf9018239openalex-snapshot
Identification of Annonaceous Acetogenins in the Ripe Fruit of the North American Pawpaw (Asimina triloba)
inferredcites →https://doi.org/10.1021/jm801028copenalex-snapshot
Alteration of the Bis-tetrahydrofuran Core Stereochemistries in Asimicin Can Affect the Cytotoxicity
inferredcites →https://doi.org/10.1021/jo000500aopenalex-snapshot
Total Synthesis of Asimicin and Bullatacin
inferredcites →https://doi.org/10.1021/jo00130a009openalex-snapshot
Acetal Templates for the Synthesis of trans-2,5-Disubstituted Tetrahydrofurans
inferredcites →https://doi.org/10.1021/jo005643bopenalex-snapshot
Enantioselective Syntheses of Monotetrahydrofuran Annonaceous Acetogenins Tonkinecin and Annonacin Starting from Carbohydrates
inferredcites →https://doi.org/10.1021/jo800514kopenalex-snapshot
Stereoselective Synthesis of 3-Oxygenated-cis-dialkyl-2,5-substituted Tetrahydrofurans from Cyclohexadienediols
inferredcites →https://doi.org/10.1021/jo961367iopenalex-snapshot
Asymmetric Dihydroxylation−Haloetherification Strategy for the Synthesis of Tetrahydrofuran-Containing Acetogenins
inferredcites →https://doi.org/10.1021/np800191topenalex-snapshot
Paw Paw and Cancer: Annonaceous Acetogenins from Discovery to Commercial Products
inferredcites →https://doi.org/10.1021/ol8025457openalex-snapshot
A Novel Approach to the CDE Ring System of Pectenotoxin-4 Triggered by VO(acac)2-Induced Epoxy-Acetalization
inferredcites →https://doi.org/10.1034/j.1399-3054.2001.1110219.xopenalex-snapshot
Annonaceous acetogenins: Naturally occurring inhibitors of ATP synthesis and photosystem II in spinach chloroplasts
inferredcites →https://doi.org/10.1039/a900200fopenalex-snapshot
The synthetic utility of furan-, pyrrole- and thiophene-based 2-silyloxy dienes
inferredcites →https://doi.org/10.1039/a900732fopenalex-snapshot
Osmylation of chiral cis-cyclohexadienediols
inferredcites →https://doi.org/10.1039/b500186mopenalex-snapshot
Acetogenins from Annonaceae: recent progress in isolation, synthesis and mechanisms of action
inferredcites →https://doi.org/10.1046/j.1432-1327.2000.01263.xopenalex-snapshot
Design syntheses and mitochondrial complex I inhibitory activity of novel acetogenin mimics
inferredcites →https://doi.org/10.1055/s-1981-29317openalex-snapshot
The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
inferredcites →https://doi.org/10.1351/pac200375020223openalex-snapshot
Chemoenzymatic methods for the enantioselective preparation of sesquiterpenoid natural products from aromatic precursors
inferredcites →https://doi.org/10.1523/jneurosci.1644-07.2007openalex-snapshot
Annonacin, a Natural Mitochondrial Complex I Inhibitor, Causes Tau Pathology in Cultured Neurons
inferredcites →https://doi.org/10.3390/molecules15010460openalex-snapshot
Total Synthesis of Annonaceous Acetogenins Belonging to the Non-Adjacent Bis-THF and Non-Adjacent THF-THP Sub-Classes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4176346openalex-extracted
Synthesis of Carbohydrate Analogues of the THF-Acetogenin 4-Deoxyannomontacin and Their Cytotoxicity Against Human Prostate Cancer Cell Lines
inferred← citeshttps://doi.org/10.1002/ajoc.202200530openalex-snapshot
Achievements, Challenges, and Scope of Thirty Years of Work on the Biotransformation of Arenes and Their Synthetic Applications
inferred← citeshttps://doi.org/10.1002/ejoc.201700494openalex-snapshot
Tetrahydrofuran Formation through Intramolecular Iodoetherification: Mechanistic Insights into the Neighbouring‐Group Participation of an Ester
inferred← citeshttps://doi.org/10.1007/978-3-031-26629-4_1openalex-snapshot
Naturally Occurring Organohalogen Compounds—A Comprehensive Review
inferred← citeshttps://doi.org/10.1016/b978-0-12-822212-6.00006-0openalex-snapshot
Enzymatic dihydroxylation of aromatic compounds: Nature's unique reaction and its impact on the synthesis of natural products
inferred← citeshttps://doi.org/10.1016/j.carres.2022.108671openalex-snapshot
Synthesis of carbohydrate analogues of the THF-acetogenin 4-deoxyannomontacin and their cytotoxicity against human prostate cancer cell lines
inferred← citeshttps://doi.org/10.1016/j.tet.2016.06.076openalex-snapshot
Recent advances in the synthesis of tetrahydrofurans and applications in total synthesis
inferred← citeshttps://doi.org/10.1039/c3qo00057eopenalex-snapshot
Benzoate dioxygenase from Ralstonia eutropha B9 – unusual regiochemistry of dihydroxylation permits rapid access to novel chirons
inferred← citeshttps://doi.org/10.1039/d1ob02496eopenalex-snapshot
Readily accessible azido-alkyne-functionalized monomers for the synthesis of cyclodextrin analogues using click chemistry
inferred← citeshttps://doi.org/10.1039/d2np00008copenalex-snapshot
Chemoenzymatic approaches to plant natural product inspired compounds
inferred← citeshttps://doi.org/10.3987/com-13-s(s)89openalex-snapshot
Chemoenzymatic Approach to Synthesis of Hydroxylated Pyrrolidines from Benzoic Acid
inferred← citeshttps://doi.org/10.4236/jacen.2015.42006openalex-snapshot
Structural Factors of Annonaceous Acetogenins and Their Semisynthetic Analogues Related with the Toxicity on Spodoptera frugiperda
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.