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Heliespirones B and C: Two New Plant Heliespiranes with a Novel Spiro Heterocyclic Sesquiterpene Skeleton
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/s0040-4039(97)10538-xopenalex-snapshot
Heliespirone A. The first member of a novel family of bioactive sesquiterpenes
inferredcites →https://doi.org/10.1016/s0040-4039(99)00833-3openalex-snapshot
Heliannuol E. A novel bioactive sesquiterpene of the heliannane family
inferredcites →https://doi.org/10.1021/jf60217a014openalex-snapshot
Gas chromatographic-mass spectral analyses of s-triazine metabolites
inferredcites →https://doi.org/10.1021/jo00105a052openalex-snapshot
Structural Elucidation and Chemistry of a Novel Family of Bioactive Sesquiterpenes: Heliannuols
inferredcites →https://doi.org/10.1021/jo00208a019openalex-snapshot
Structures and stereochemistries of oscillatoxin B, 31-noroscillatoxin B, oscillatoxin D, and 30-methyloscillatoxin D
inferredcites →https://doi.org/10.1021/jo00208a020openalex-snapshot
Synthesis of 3-aryl-3,4-dihydroisocoumarins
inferredcites →https://doi.org/10.1021/jo981881jopenalex-snapshot
Prunolides A, B, and C: Novel Tetraphenolic Bis-Spiroketals from the Australian Ascidian Synoicum prunum
inferredcites →https://doi.org/10.1021/np990249yopenalex-snapshot
New Bioactive Plant Heliannuols from Cultivar Sunflower Leaves
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Inverse Electron Demand Diels-Alder Reaction in Total Synthesis of Bioactive Natural Products
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Sequential Reactions Initiated by Oxidative Dearomatization. Biomimicry or Artifact?
inferred← citeshttps://doi.org/10.1002/adsc.200900864openalex-snapshot
Divergent Reactivity of 2‐Azetidinone‐Tethered Allenols with Electrophilic Reagents: Controlled Ring Expansion versus Spirocyclization
inferred← citeshttps://doi.org/10.1002/adsc.201301153openalex-snapshot
Advancement in Cascade [1,n]‐Hydrogen Transfer/Cyclization: A Method for Direct Functionalization of Inactive C(sp3)H Bonds
inferred← citeshttps://doi.org/10.1002/ange.200904565openalex-snapshot
Brønsted Acid Catalyzed Enantioselective Semipinacol Rearrangement for the Synthesis of Chiral Spiroethers
inferred← citeshttps://doi.org/10.1002/ange.201204274openalex-snapshot
Organocatalytic Asymmetric Direct CH Functionalization of Ethers: A Highly Efficient Approach to Chiral Spiroethers
inferred← citeshttps://doi.org/10.1002/anie.200904565openalex-snapshot
Brønsted Acid Catalyzed Enantioselective Semipinacol Rearrangement for the Synthesis of Chiral Spiroethers
inferred← citeshttps://doi.org/10.1002/anie.201204274openalex-snapshot
Organocatalytic Asymmetric Direct CH Functionalization of Ethers: A Highly Efficient Approach to Chiral Spiroethers
inferred← citeshttps://doi.org/10.1002/chin.200705176openalex-snapshot
Heliespirones B and C: Two New Plant Heliespiranes with a Novel Spiro Heterocyclic Sesquiterpene Skeleton.
inferred← citeshttps://doi.org/10.1002/ejoc.201402420openalex-snapshot
Total Synthesis of (–)‐Heliespirone A and (+)‐Heliespirone C
inferred← citeshttps://doi.org/10.1002/ejoc.201403087openalex-snapshot
Diastereoselective Synthesis of Spirocyclic Dihydrofurans and 1‐Oxaspiro[4.5]decan‐6‐one Derivatives from Norbornyl α‐Diketones
inferred← citeshttps://doi.org/10.1002/ejoc.202300626openalex-snapshot
Julia‐Kocienski Olefination in the Synthesis of Trisubstituted Alkenes: Recent Progress
inferred← citeshttps://doi.org/10.1002/ejoc.202400267openalex-snapshot
High Yield Synthesis of Spirocyclic Dienones from Phenols Employing Tribromide Catalysed Dearomatization
inferred← citeshttps://doi.org/10.1007/7081_2019_32openalex-snapshot
Carbohydrate-Derived Spiroketals and Spirocyclic Lactones
inferred← citeshttps://doi.org/10.1007/978-3-030-52966-6_1openalex-snapshot
Allelopathy: The Chemical Language of Plants
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_2openalex-snapshot
Classification of Diverse Novel Sesquiterpenoids
inferred← citeshttps://doi.org/10.1007/s11101-023-09903-xopenalex-snapshot
Terpenoid diversity in sunflower (Helianthus annuus L.) and their potential in crop protection
inferred← citeshttps://doi.org/10.1007/s11426-010-4173-yopenalex-snapshot
Racemic and enantioselective total synthesis of heliespirones A & C
inferred← citeshttps://doi.org/10.1007/s11426-016-0076-6openalex-snapshot
Recent advances in terpenoid syntheses from China
inferred← citeshttps://doi.org/10.1007/s41061-016-0018-2openalex-snapshot
Hydrogen-Atom Transfer Reactions
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.09.042openalex-snapshot
SAR studies of epoxycurcuphenol derivatives on leukemia CT-CD4 cells
inferred← citeshttps://doi.org/10.1016/j.phytol.2022.10.003openalex-snapshot
A pair of new sesquiterpene isomers containing spiro heterocyclic skeleton from plant-derived fungus Botryosphaeria dothidea
inferred← citeshttps://doi.org/10.1016/j.tchem.2024.100066openalex-snapshot
Inverse electron demand Diels-Alder reaction in total synthesis of bioactive natural products
inferred← citeshttps://doi.org/10.1016/j.tet.2011.03.064openalex-snapshot
Enantioselective syntheses of the assigned structures of the helibisabonols A and B
inferred← citeshttps://doi.org/10.1016/j.tet.2014.06.025openalex-snapshot
Protecting group-free syntheses of natural products and biologically active compounds
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.08.131openalex-snapshot
Asymmetric total syntheses of heliannuol E and epi-heliannuol E
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.12.115openalex-snapshot
Enantioselective total synthesis of heliespirone B
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.06.093openalex-snapshot
Total synthesis of heliespirone B
inferred← citeshttps://doi.org/10.1016/s0959-6380(02)80009-5openalex-snapshot
Chapter 5.3 Five-membered ring systems: Furans and benzofurans
inferred← citeshttps://doi.org/10.1016/s0959-6380(08)80009-8openalex-snapshot
Chapter 5.3 Five-membered ring systems: furans and benzofurans
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00953openalex-snapshot
Diastereoselective Synthesis of CF3- and CF2H-Substituted Spiroethers from Aryl-Fused Cycloalkenylalkanols by Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.7b03196openalex-snapshot
A Convergent Approach to Diverse Spiroethers through Stereoselective Trapping of Rhodium Carbenoids with Gold-Activated Alkynols
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02143openalex-snapshot
Electrochemical Promoted Three-Component Trifluoromethylation/Spirocyclization Reaction of N-Arylsulfonylacrylamides to 4-Azaspiro[4.5]decanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04324openalex-snapshot
Chemoselective Oxidative Spiroetherification and Spiroamination of Arenols Using I+/Oxone Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04658openalex-snapshot
Enantioselective Iridium-Catalyzed α-Allylation with Aqueous Solutions of Acetaldehyde
inferred← citeshttps://doi.org/10.1021/jo201971gopenalex-snapshot
Total Syntheses of ent-Heliespirones A and C
inferred← citeshttps://doi.org/10.1021/jo3016055openalex-snapshot
Total Synthesis of Natural Enantiomers of Heliespirones A and C via the Diastereoselective Intramolecular Hosomi-Sakurai Reaction
inferred← citeshttps://doi.org/10.1021/ol303263qopenalex-snapshot
Rapid and Stereoselective Synthesis of Spirocyclic Ethers via the Intramolecular Piancatelli Rearrangement
inferred← citeshttps://doi.org/10.1021/ol800854sopenalex-snapshot
Asymmetric Synthesis of Spiroketal, Spiroether, and Oxabicycle Building Blocks via Stereoselective Spiro- and Bicycloannulation of 2-Hydroxy Dihydropyrans
inferred← citeshttps://doi.org/10.1039/c0cc00481bopenalex-snapshot
Asymmetric total synthesis of ent-heliespirones A & C
inferred← citeshttps://doi.org/10.1039/c3ob40284copenalex-snapshot
Convergent approach to complex spirocyclic pyrans: practical synthesis of the oxa-pinnaic acid core
inferred← citeshttps://doi.org/10.1039/c3ra48040bopenalex-snapshot
Heterocyclic terpenes: linear furano- and pyrroloterpenoids
inferred← citeshttps://doi.org/10.1039/c5ra27899fopenalex-snapshot
CuI-catalyzed oxidative cross coupling of oximes with tetrahydrofuran: a direct access to O-tetrahydrofuran-2-yl oxime ethers
inferred← citeshttps://doi.org/10.1071/ch18019openalex-snapshot
Synthesis of Highly Enantio-Enriched Heliespirones A and C by a Diastereoselective Aromatic Claisen Rearrangement
inferred← citeshttps://doi.org/10.1351/pac-con-11-10-34openalex-snapshot
New strategies for natural products containing chroman spiroketals
inferred← citeshttps://doi.org/10.1590/s0102-33062013000100009openalex-snapshot
Phytotoxic activity of crude aqueous extracts and fractions of young leaves of Sapindus saponaria L. (Sapindaceae)
inferred← citeshttps://doi.org/10.3390/molecules24224165openalex-snapshot
Spirocyclic Motifs in Natural Products
inferred← citeshttps://doi.org/10.3762/bjoc.9.262openalex-snapshot
Elucidation of the regio- and chemoselectivity of enzymatic allylic oxidations with Pleurotus sapidus – conversion of selected spirocyclic terpenoids and computational analysis
inferred← citeshttps://doi.org/10.3987/com-08-s(d)22openalex-snapshot
Stereoselective Synthesis of 5-Substituted 2-Allyl-3-oxotetrahydrofuran-2-carboxylates Using Rhodium(II)-Catalyzed Oxonium Ylide Formation–[2,3] Shift
inferred← citeshttps://doi.org/10.70675/6026cebfzde60z463czaa3czdffdcb7fd521openalex-snapshot
Synthèse d'hétérospirocycles par hydroaminations et hydroalkoxylations d'alcynes catalysées par l'or (I) - Méthodologie et application au développement de fragments spirocycliques pour la chimie médicinale.
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