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Total Syntheses of Parthenolide and Its Analogues with Macrocyclic Stereocontrol

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

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Allylation of Carbonyls: Methodology and Stereochemistry

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Total Synthesis of Amphidinolide T4

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Photochemical Reactions as Key Steps in Natural Product Synthesis

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Cover Picture: A Diagonal Approach to Chemical Recycling of Carbon Dioxide: Organocatalytic Transformation for the Reductive Functionalization of CO2 (Angew. Chem. Int. Ed. 1/2012)

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Towards the Synthesis of Highly Functionalized Chiral α‐Amino Nitriles by Aminative Cyanation and Their Synthetic Applications

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Sesquiterpene lactones from Michelia champaca

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Acid cyclization of 5-ketogermacren-6,12-olides. A reactivity and conformational study

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Indium mediated intramolecular carbocyclization in aqueous media. A facile and stereoselective synthesis of fused α-methylene-γ-butyrolactones

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Purification of Laboratory Chemicals

inferredcites →https://doi.org/10.1016/j.bmc.2010.12.045openalex-snapshot

Melampomagnolide B: A new antileukemic sesquiterpene

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

Microtubule-interfering activity of parthenolide

inferredcites →https://doi.org/10.1016/j.drudis.2009.08.008openalex-snapshot

New agents for the treatment of leukemia: discovery of DMAPT (LC-1)

inferredcites →https://doi.org/10.1016/j.drudis.2013.05.005openalex-snapshot

Parthenolide: from plant shoots to cancer roots

inferredcites →https://doi.org/10.1016/j.tet.2008.09.017openalex-snapshot

Substituent effects in the transannular cyclizations of germacranes. Synthesis of 6-epi-costunolide and five natural steiractinolides

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Chiral 1,4-morpholin-2,5-dione derivatives as α-glucosidase inhibitors: Part 2

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Fungicidal activity of natural and synthetic sesquiterpene lactone analogs

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Allelochemicals from sunflower leaves cv. Peredovick

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Macroring contraction methodology

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Chemical consequences of conformation in macrocyclic compounds

inferredcites →https://doi.org/10.1016/s0040-4020(99)00025-3openalex-snapshot

The synthesis of germacrane sesquiterpenes and related compounds

inferredcites →https://doi.org/10.1016/s0040-4039(00)61275-3openalex-snapshot

Partial synthesis of germacranolides with pyran and furan-type rings

inferredcites →https://doi.org/10.1016/s0040-4039(97)10750-xopenalex-snapshot

Extremely convenient cyclization of medium rings using SmI2

inferredcites →https://doi.org/10.1016/s0960-894x(99)00529-6openalex-snapshot

Stereoselective synthesis of non symmetric dihydroxyethylene dipeptide isosteres via epoxyalcohols derived from α-amino acids

inferredcites →https://doi.org/10.1016/s0968-0896(02)00553-9openalex-snapshot

Parthenolide and its photochemically synthesized 1(10)Z isomer: chemical reactivity and structure–activity relationship studies in human leucocyte chemotaxis

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The anti-inflammatory natural product parthenolide from the medicinal herb Feverfew directly binds to and inhibits IκB kinase

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Photochemical one-way adiabatic isomerization of aromatic olefins

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Total synthesis of furanocembranolides. 2. Macrocyclization studies culminating in the synthesis of a dihydropseudopterolide and gorgiacerone. Related furanocembranolide interconversions.

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Enantioselective complexation of organic ammonium ions by simple tetracyclic podand ionophores

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General methodology for the synthesis of neocarzinostatin chromophore analogs: intramolecular chromium-mediated closures for strained ring synthesis

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Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization

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Macrocyclic stereocontrol. Total synthesis of (.+-.)-3-deoxyrosaranolide

inferredcites →https://doi.org/10.1021/ja00341a055openalex-snapshot

Synthesis of the cytotoxic germacranolide eucannabinolide

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Synthetic methods for sesquiterpene .alpha.-methylene-.gamma.-lactones

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The first practical method for asymmetric epoxidation

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Enantioselective Total Synthesis of (+)-Amphidinolide T1

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Titanium(II)-Mediated Cyclizations of (Silyloxy)enynes: A Total Synthesis of (−)-7-Demethylpiericidin A 1

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Simple Reagents for Direct Halonium-Induced Polyene Cyclizations

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Sesquiterpenes wth ten-membered carbon rings. Review

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A straightforward approach to the synthesis of the tricyclic core of taxol

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Acid cyclization and other products of the germacranolide epoxide, lipiferolide

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Synthesis of asperdiol

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[2,3]-Wittig rearrangement of a 13-membered diallylic ether. Six-step synthesis of costunolide

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Preparation of 2-(alkylthiomethyl)acrylates

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Biomimetic Semisynthesis of Arglabin from Parthenolide

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Protection-Group-Free Semisyntheses of Parthenolide and Its Cyclopropyl Analogue

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Sesquiterpene Lactones from Staehelina fruticosa

inferredcites →https://doi.org/10.1021/np960064gopenalex-snapshot

Antitumor Germacranolides from Anvillea garcinii

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Structure−Cytotoxicity Relationships of Some Helenanolide-Type Sesquiterpene Lactones

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γ-Hydroxynitrile Alkylations: Electrophile-Dependent Stereoselectivity

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Concise Total Synthesis of (−)-8-Epigrosheimin

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The root of the problem

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Natural sesquiterpenoids

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Antiplasmodial Activities and Cytotoxic Effects of Aqueous Extracts and Sesquiterpene Lactones fromNeurolaena lobata*

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Parthenolide, a sesquiterpene lactone from the medical herb feverfew, shows anticancer activity against human melanoma cells in vitro

inferredcites →https://doi.org/10.1128/aac.49.11.176-182.2005openalex-snapshot

Antileishmanial Activity of Parthenolide, a Sesquiterpene Lactone Isolated from Tanacetum parthenium

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Sulforaphane, a Dietary Component of Broccoli/Broccoli Sprouts, Inhibits Breast Cancer Stem Cells

inferredcites →https://doi.org/10.1182/blood-2004-10-4135openalex-snapshot

The sesquiterpene lactone parthenolide induces apoptosis of human acute myelogenous leukemia stem and progenitor cells

inferredcites →https://doi.org/10.1208/pt0804105openalex-snapshot

The solution and solid state stability and excipient compatibility of parthenolide in feverfew

inferredcites →https://doi.org/10.1248/cpb.38.28openalex-snapshot

Studies on the terpenoids and related alicyclic compounds XXXIX. A synthesis of .ALPHA.-methylene-.GAMMA.-lactones fused to medium and large rings by intramolecular cyclization of formylated allyl halides.

What points at this work

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

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Visible‐Light Photocatalysis of the Ketyl Radical Coupling Reaction

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Structure-activity relationship studies on anti-cancer bioactive natural products

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Parthenolide and Parthenolide-Like Sesquiterpene Lactones as Multiple Targets Drugs

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Natural STAT3 inhibitors: A mini perspective

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Chalcone: A potential scaffold for NLRP3 inflammasome inhibitors

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Synthesis and anti-acute myeloid leukemia activity of C-14 modified parthenolide derivatives

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Design and synthesis of parthenolide and 5-fluorouracil conjugates as potential anticancer agents against drug resistant hepatocellular carcinoma

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Elephantopinolide A-P, germacrane-type sesquiterpene lactones from Elephantopus scaber induce apoptosis, autophagy and G2/M phase arrest in hepatocellular carcinoma cells

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Discovery of novel fluorine-containing parthenolide analogues as potential antitumor agents

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Elephantopus scaber suppresses ConA-induced T cell activation by inhibiting NF-κB and Ca2+/NFAT signaling

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