On the public citation graph

Sequencing of Three-Component Olefin Metatheses: Total Synthesis of Either (+)-Gigantecin or (+)-14-Deoxy-9-oxygigantecin

0 signed · 65 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.

Claim with ORCID

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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/anie.200390252openalex-snapshot

A Highly Practical and Enantioselective Reagent for the Allylation of Aldehydes

inferredcites →https://doi.org/10.1002/anie.200390253openalex-snapshot

A General Oxidative Cyclization of 1,5‐Dienes Using Catalytic Osmium Tetroxide

inferredcites →https://doi.org/10.1002/chin.200325028openalex-snapshot

A Highly Practical and Enantioselective Reagent for the Allylation of Aldehydes.

inferredcites →https://doi.org/10.1007/bf01954260openalex-snapshot

Gigantecin: A novel antimitotic and cytotoxic acetogenin, with nonadjacent tetrahydrofuran rings, fromGoniothalamus giganteus (Annonaceae)

inferredcites →https://doi.org/10.1021/ar000114fopenalex-snapshot

The Development of L 2 X 2 RuCHR Olefin Metathesis Catalysts: An Organometallic Success Story

inferredcites →https://doi.org/10.1021/ja001179gopenalex-snapshot

Efficient and Recyclable Monomeric and Dendritic Ru-Based Metathesis Catalysts

inferredcites →https://doi.org/10.1021/ja0214882openalex-snapshot

A General Model for Selectivity in Olefin Cross Metathesis

inferredcites →https://doi.org/10.1021/np50068a001openalex-snapshot

Annonaceous Acetogenins: A Review

inferredcites →https://doi.org/10.1021/ol0512886openalex-snapshot

Multivalent Activation in Temporary Phosphate Tethers: A New Tether for Small Molecule Synthesis

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/10.1002/0471264180.or089.01openalex-snapshot

Olefin Ring‐Closing Metathesis

inferred← citeshttps://doi.org/10.1002/0471264180.or106.01openalex-snapshot

Alkene Cross‐Metathesis Reactions

inferred← citeshttps://doi.org/10.1002/9781118342886.ch5openalex-snapshot

Metathesis‐Based Synthesis of Complex Bioactives

inferred← citeshttps://doi.org/10.1002/9781118711613.ch8openalex-snapshot

Applications in the Synthesis of Natural and Biologically Active Molecules

inferred← citeshttps://doi.org/10.1002/9783527629626.ch10openalex-snapshot

Cross‐Metathesis in Natural Products Synthesis

inferred← citeshttps://doi.org/10.1002/9783527629626.ch8openalex-snapshot

Temporary Silicon–Tethered Ring–Closing Metathesis Reactions in Natural Product Synthesis

inferred← citeshttps://doi.org/10.1002/9783527674107.ch16openalex-snapshot

Cross‐Metathesis

inferred← citeshttps://doi.org/10.1002/9783527674107.ch23openalex-snapshot

Metathesis of Silicon‐Containing Olefins

inferred← citeshttps://doi.org/10.1002/ange.200700501openalex-snapshot

Chiral N‐Heterocyclic Carbenes in Natural Product Synthesis: Application of Ru‐Catalyzed Asymmetric Ring‐Opening/Cross‐Metathesis and Cu‐Catalyzed Allylic Alkylation to Total Synthesis of Baconipyrone C

inferred← citeshttps://doi.org/10.1002/ange.201005044openalex-snapshot

Allylmalonate as an Activator Subunit for the Initiation of Relay Ring‐Closing Metathesis Reactions

inferred← citeshttps://doi.org/10.1002/anie.200700501openalex-snapshot

inferred← citeshttps://doi.org/10.1002/anie.201005044openalex-snapshot

Allylmalonate as an Activator Subunit for the Initiation of Relay Ring‐Closing Metathesis Reactions

inferred← citeshttps://doi.org/10.1002/asia.202000955openalex-snapshot

Muricatacin, a Gateway Molecule to Higher Acetogenin Synthesis

inferred← citeshttps://doi.org/10.1002/cbic.200600411openalex-snapshot

A Structure–Activity Guided Strategy for Fluorescent Labeling of Annonaceous Acetogenin Mimetics and their Application in Cell Biology

inferred← citeshttps://doi.org/10.1002/chem.200801298openalex-snapshot

Tuning the Acyclic Ether Moiety of Anticancer Agent AA005 with Conformationally Constrained Fragments

inferred← citeshttps://doi.org/10.1002/chem.201103186openalex-snapshot

Temporary Silicon‐Tethered Ring‐Closing Metathesis: Recent Advances in Methodology Development and Natural Product Synthesis

inferred← citeshttps://doi.org/10.1002/chem.201203067openalex-snapshot

Synthesis of the Originally Proposed Structure of Palmerolide C

inferred← citeshttps://doi.org/10.1002/ejoc.200600946openalex-snapshot

Tandem Sequential Ring‐Closing Metathesis/Diels–Alder/Cross‐Metathesis: Formation of Polycyclic Compounds by a New Three‐Component Reaction

inferred← citeshttps://doi.org/10.1002/ejoc.201000875openalex-snapshot

Convergent Total Synthesis of Murisolin

inferred← citeshttps://doi.org/10.1002/ejoc.202000665openalex-snapshot

A Decade of Muricatacin Synthesis and Beyond

inferred← citeshttps://doi.org/10.1002/hlca.201300313openalex-snapshot

Synthesis of a Benzannulated Pyrrolizidine by a Copper‐Catalyzed Intramolecular α‐Arylation Reaction

inferred← citeshttps://doi.org/10.1007/128_2012_318openalex-snapshot

Selective Alkene Metathesis in the Total Synthesis of Complex Natural Product

inferred← citeshttps://doi.org/10.1007/7081_2015_162openalex-snapshot

Synthesis of P-, S-, Si-, B-, and Se-Heterocycles via Ring-Closing Metathesis

inferred← citeshttps://doi.org/10.1007/978-3-319-22692-7_2openalex-snapshot

Acetogenins from Annonaceae

inferred← citeshttps://doi.org/10.1016/j.bmc.2007.02.002openalex-snapshot

Synthesis, determination of the absolute configuration of tonkinelin, and inhibitory action with bovine heart mitochondrial complex I

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.03.084openalex-snapshot

Annonaceous acetogenin mimics bearing a terminal lactam and their cytotoxicity against cancer cells

inferred← citeshttps://doi.org/10.1016/j.bmcl.2008.10.069openalex-snapshot

Synthesis of C4-fluorinated solamins and their growth inhibitory activity against human cancer cell lines

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.2007.03.151openalex-snapshot

Convergent total synthesis of squamostolide

inferred← citeshttps://doi.org/10.1016/j.tet.2010.08.028openalex-snapshot

Synthesis of solamin type mono-THF acetogenins using cross-metathesis

inferred← citeshttps://doi.org/10.1016/j.tet.2013.01.017openalex-snapshot

Selective deprotection of silyl ethers

inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.11.190openalex-snapshot

Total synthesis of cis-solamin A, a mono-tetrahydrofuran acetogenin isolated from Annona muricata

inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.07.121openalex-snapshot

Comparing and taming the reactivity of HWE and Wittig reagents with cyclic hemiacetals

inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.11.032openalex-snapshot

Two-directional synthesis of the non-adjacent bis(tetrahydrofuran) core of cis-sylvaticin

inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.05.064openalex-snapshot

Synthesis of the non-adjacent bis(tetrahydrofuran) core of squamostanin C by silicon-tethered, size-selective triple ring-closing metathesis

inferred← citeshttps://doi.org/10.1016/s1875-5364(19)30032-9openalex-snapshot

Eight new cytotoxic annonaceous acetogenins from the seeds of Annona squamosa

inferred← citeshttps://doi.org/10.1021/acs.joc.2c00262openalex-snapshot

Synthetic Efforts and Ultimate Limitation to an Asymmetric Achmatowicz Approach Toward EBC-23

inferred← citeshttps://doi.org/10.1021/acs.joc.5b02473openalex-snapshot

Phosphate Tether-Mediated Ring-Closing Metathesis for the Generation of P-Stereogenic, Z-Configured Bicyclo[7.3.1]- and Bicyclo[8.3.1]phosphates

inferred← citeshttps://doi.org/10.1021/acs.oprd.4c00101openalex-snapshot

Synthetic Process Development of ( R )-(+)-1,2-Epoxy-5-hexene: An Important Chiral Building Block

inferred← citeshttps://doi.org/10.1021/ja0660148openalex-snapshot

Total Synthesis of (+)-cis-Sylvaticin: Double Oxidative Cyclization Reactions Catalyzed by Osmium

inferred← citeshttps://doi.org/10.1021/ja505639uopenalex-snapshot

Total Synthesis of Tetrahydrolipstatin and Stereoisomers via a Highly Regio- and Diastereoselective Carbonylation of Epoxyhomoallylic Alcohols

inferred← citeshttps://doi.org/10.1021/ja9049959openalex-snapshot

Concise Syntheses of the Natural Products (+)-Sylvaticin and (+)-cis-Sylvaticin

inferred← citeshttps://doi.org/10.1021/jm800979vopenalex-snapshot

Improved Synthesis of 6-epi-Dictyostatin and Antitumor Efficacy in Mice Bearing MDA-MB231 Human Breast Cancer Xenografts

inferred← citeshttps://doi.org/10.1021/jm801028copenalex-snapshot

Alteration of the Bis-tetrahydrofuran Core Stereochemistries in Asimicin Can Affect the Cytotoxicity

inferred← citeshttps://doi.org/10.1021/jo3004106openalex-snapshot

Total Synthesis of (−)-Goniotrionin

inferred← citeshttps://doi.org/10.1021/ol800767eopenalex-snapshot

Total Synthesis of cis-Sylvaticin

inferred← citeshttps://doi.org/10.1039/b813201aopenalex-snapshot

Synthesis of the non-adjacent bis-THF core of cis-sylvaticin using a double oxidative cyclisation

inferred← citeshttps://doi.org/10.1055/s-0030-1250006openalex-snapshot

Historic Perspectives on Annonaceous Acetogenins from the Chemical Bench to Preclinical Trials

inferred← citeshttps://doi.org/10.1271/bbb.70202openalex-snapshot

Synthesis of Annonaceous Acetogenins from Muricatacin

inferred← citeshttps://doi.org/10.3390/antiox9121220openalex-snapshot

Discovery of Spilanthol Endoperoxide as a Redox Natural Compound Active against Mammalian Prx3 and Chlamydia trachomatis Infection

inferred← citeshttps://doi.org/10.3390/md21080453openalex-snapshot

Trichoderols B-G, Six New Lipids from the Marine Algicolous Fungus Trichoderma sp. Z43

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.3762/bjoc.4.48openalex-snapshot

Recent progress on the total synthesis of acetogenins from Annonaceae

inferred← citeshttps://doi.org/10.3987/com-08-s(d)45openalex-snapshot

Convergent Synthesis of Fluorescence Labeled Solamin

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.