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Total Synthesis of the Meroterpenoid Manginoid A as Fueled by a Challenging Pinacol Coupling and Bicycle‐forming Etherification
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ange.200502485openalex-snapshot
Lösliche Lanthanoid‐Salze (LnCl3⋅2 LiCl) für die verbesserte Addition magnesiumorganischer Reagentien an Carbonylverbindungen
inferredcites →https://doi.org/10.1002/ange.200803247openalex-snapshot
Enantioselective Cu‐Catalyzed 1,4‐Addition of Grignard Reagents to Cyclohexenone Using Taddol‐Derived Phosphine–Phosphite Ligands and 2‐Methyl‐THF as a Solvent
inferredcites →https://doi.org/10.1002/ange.200902151openalex-snapshot
Samariumdiiodid‐vermittelte Reaktionen in der Totalsynthese
inferredcites →https://doi.org/10.1002/ange.201101654openalex-snapshot
Allylic CH Alkylation of Unactivated α‐Olefins: Serial Ligand Catalysis Resumed
inferredcites →https://doi.org/10.1002/ange.201812909openalex-snapshot
Total Synthesis and Anticancer Activity of (+)‐Hypercalin C and Congeners
inferredcites →https://doi.org/10.1002/ange.201906872openalex-snapshot
Total Synthesis of 1‐Hydroxytaxinine
inferredcites →https://doi.org/10.1002/ange.201915876openalex-snapshot
Total Synthesis of (−)‐Pepluanol B: Conformational Control of the Eight‐Membered‐Ring System
inferredcites →https://doi.org/10.1002/anie.200502485openalex-snapshot
Soluble Lanthanide Salts (LnCl 3 ⋅2 LiCl) for the Improved Addition of Organomagnesium Reagents to Carbonyl Compounds
inferredcites →https://doi.org/10.1002/anie.200803247openalex-snapshot
Enantioselective Cu‐Catalyzed 1,4‐Addition of Grignard Reagents to Cyclohexenone Using Taddol‐Derived Phosphine–Phosphite Ligands and 2‐Methyl‐THF as a Solvent
inferredcites →https://doi.org/10.1002/anie.200902151openalex-snapshot
Samarium Diiodide Mediated Reactions in Total Synthesis
inferredcites →https://doi.org/10.1002/anie.201101654openalex-snapshot
Allylic CH Alkylation of Unactivated α‐Olefins: Serial Ligand Catalysis Resumed
inferredcites →https://doi.org/10.1002/anie.201812909openalex-snapshot
Total Synthesis and Anticancer Activity of (+)‐Hypercalin C and Congeners
inferredcites →https://doi.org/10.1002/anie.201906872openalex-snapshot
Total Synthesis of 1‐Hydroxytaxinine
inferredcites →https://doi.org/10.1002/anie.201915876openalex-snapshot
Total Synthesis of (−)‐Pepluanol B: Conformational Control of the Eight‐Membered‐Ring System
inferredcites →https://doi.org/10.1007/bf00699987openalex-snapshot
Michael reactions withtrans-3-isopropenyl-2-phenylthiocyclopentan-1-one andtrans-3-isopropenyl-2-phenylsulfonylcyclopentan-1-one
inferredcites →https://doi.org/10.1007/bf00699988openalex-snapshot
Synthesis of 1,4-dimethylhydroazulene derivatives fromtrans-3-isopropenyl-2-(2-methoxycarbonylethyl)cyclopentanone
inferredcites →https://doi.org/10.1007/s13659-014-0007-5openalex-snapshot
Hypercohones D–G, New Polycyclic Polyprenylated Acylphloroglucinol Type Natural Products from Hypericum cohaerens
inferredcites →https://doi.org/10.1016/j.ejphar.2014.10.053openalex-snapshot
Pharmacological characterization of the selective 11β-hydroxysteroid dehydrogenase 1 inhibitor, BI 135585, a clinical candidate for the treatment of type 2 diabetes
inferredcites →https://doi.org/10.1016/j.phytochem.2019.05.018openalex-snapshot
Mangiterpenes A–C and 2′,3′-seco-manginoid C, four sesquiterpene/monoterpene–shikimate–conjugated spirocyclic meroterpenoids from Guignardia mangiferae
inferredcites →https://doi.org/10.1016/j.tetasy.2011.04.018openalex-snapshot
Chiral phosphine–phosphite ligands in the enantioselective 1,4-addition of Grignard reagents to α,β-unsaturated carbonyl compounds
inferredcites →https://doi.org/10.1016/j.tetlet.2008.05.147openalex-snapshot
Enantioselective rhodium(I)-triethylamine catalyzed addition of potassium isopropenyl trifluoroborate to enones
inferredcites →https://doi.org/10.1016/j.tetlet.2017.02.023openalex-snapshot
Construction of bicyclic systems containing an oxygen bridge by isomerization of cyclic epoxy alcohols
inferredcites →https://doi.org/10.1016/s0040-4039(97)01593-1openalex-snapshot
An IMDA approach to tigliane and daphnane diterpenoids: Generation of the tetracyclic ring system of the tiglianes
inferredcites →https://doi.org/10.1021/acs.orglett.0c00241openalex-snapshot
Asymmetric Total Synthesis of (−)-Guignardones A and B
inferredcites →https://doi.org/10.1021/acs.orglett.7b02955openalex-snapshot
Manginoids A–G: Seven Monoterpene–Shikimate-Conjugated Meroterpenoids with a Spiro Ring System from Guignardia mangiferae
inferredcites →https://doi.org/10.1021/acs.orglett.7b03681openalex-snapshot
Asymmetric Synthesis and Biological Activities of Pactamycin-Inspired Aminocyclopentitols
inferredcites →https://doi.org/10.1021/acs.orglett.9b00486openalex-snapshot
Asymmetric Synthesis and Structure Revision of Guignardone H and I: Development of a Chiral 1,3-Diketone Possessing C2 Symmetry
inferredcites →https://doi.org/10.1021/cr030017aopenalex-snapshot
Samarium(II)-Iodide-Mediated Cyclizations in Natural Product Synthesis
inferredcites →https://doi.org/10.1021/cr400685ropenalex-snapshot
Cross-Coupling Reactions Using Samarium(II) Iodide
inferredcites →https://doi.org/10.1021/ja001260jopenalex-snapshot
Reactions of SmI2 with Alkyl Halides and Ketones: Inner-Sphere vs Outer-Sphere Electron Transfer in Reactions of Sm(II) Reductants
inferredcites →https://doi.org/10.1021/ja00342a080openalex-snapshot
Stereocontrol in homogeneous catalytic hydrogenation via hydroxyl group coordination
inferredcites →https://doi.org/10.1021/ja00384a077openalex-snapshot
The endiandric acid cascade. Electrocyclizations in organic synthesis. I. Stepwise, stereocontrolled total synthesis of endiandric acids A and B
inferredcites →https://doi.org/10.1021/ja500726eopenalex-snapshot
General Allylic C–H Alkylation with Tertiary Nucleophiles
inferredcites →https://doi.org/10.1021/ja806867popenalex-snapshot
Catalytic Intermolecular Allylic C—H Alkylation
inferredcites →https://doi.org/10.1021/ja953060ropenalex-snapshot
General Strategy for the Asymmetric Synthesis of the Picrotoxanes
inferredcites →https://doi.org/10.1021/ja9543098openalex-snapshot
On Pd-Catalyzed Cycloisomerization versus Cycloreduction. A General Strategy for Drimane Synthesis and a Short Total Synthesis of Siccanin
inferredcites →https://doi.org/10.1021/jacs.6b00567openalex-snapshot
Catalytic Asymmetric Total Synthesis of (−)-Actinophyllic Acid
inferredcites →https://doi.org/10.1021/jacs.6b06623openalex-snapshot
11-Step Total Synthesis of (−)-Maoecrystal V
inferredcites →https://doi.org/10.1021/jacs.6b10397openalex-snapshot
Annulative Methods Enable a Total Synthesis of the Complex Meroterpene Berkeleyone A
inferredcites →https://doi.org/10.1021/jacs.7b01734openalex-snapshot
A Concise, Efficient and Scalable Total Synthesis of Thapsigargin and Nortrilobolide from (R)-(−)-Carvone
inferredcites →https://doi.org/10.1021/jacs.7b13260openalex-snapshot
Total Synthesis of (+)-Pleuromutilin
inferredcites →https://doi.org/10.1021/jacs.8b01918openalex-snapshot
Total Synthesis of the Norhasubanan Alkaloid Stephadiamine
inferredcites →https://doi.org/10.1021/jacs.8b05668openalex-snapshot
Asymmetric Allylic C–H Alkylation via Palladium(II)/cis-ArSOX Catalysis
inferredcites →https://doi.org/10.1021/jacs.9b05815openalex-snapshot
Total Synthesis of the Diterpenoid Alkaloid Arcutinidine Using a Strategy Inspired by Chemical Network Analysis
inferredcites →https://doi.org/10.1021/jo00219a054openalex-snapshot
Manganese(III)-based oxidative free-radical cyclization. Synthesis of (.+-.)-podocarpic acid
inferredcites →https://doi.org/10.1021/jo00295a035openalex-snapshot
Manganese(III)-based oxidative free-radical cyclization of unsaturated .beta.-keto esters, 1,3-diketones, and malonate diesters
inferredcites →https://doi.org/10.1021/jo00357a040openalex-snapshot
Lanthanides in organic synthesis. 2. Reduction of .alpha.-heterosubstituted ketones
inferredcites →https://doi.org/10.1021/jo980831bopenalex-snapshot
A Highly Efficient Pinacol Coupling Approach to Trehazolamine Starting from d -Glucose
inferredcites →https://doi.org/10.1021/jo990484lopenalex-snapshot
Structure and Energetics of the Samarium Diiodide−HMPA Complex in Tetrahydrofuran
inferredcites →https://doi.org/10.1021/ol0613517openalex-snapshot
1-Silyl-2,6-diketones: Versatile Intermediates for the Divergent Synthesis of Five- and Six-Membered Carbocycles under Radical and Anionic Conditions
inferredcites →https://doi.org/10.1021/ol2021548openalex-snapshot
Biyoulactones A–C, New Pentacyclic Meroterpenoids from Hypericum chinense
inferredcites →https://doi.org/10.1021/ol3013167openalex-snapshot
A Reductive-Heck Approach to the Hydroazulene Ring System: A Formal Synthesis of the Englerins
inferredcites →https://doi.org/10.1021/ol7027898openalex-snapshot
Synthesis of Natural Products from the Indian Neem TreeAzadirachta indica
inferredcites →https://doi.org/10.1038/s41586-019-1179-2openalex-snapshot
Quaternary-centre-guided synthesis of complex polycyclic terpenes
inferredcites →https://doi.org/10.1038/s41586-019-1580-xopenalex-snapshot
A 16-step synthesis of the isoryanodane diterpene (+)-perseanol
inferredcites →https://doi.org/10.1039/c6qo00620eopenalex-snapshot
Furanmonogones A and B: two rearranged acylphloroglucinols with a 4,5-seco-3(2H)-furanone core from the flowers of Hypericum monogynum
inferredcites →https://doi.org/10.1039/d0sc04686hopenalex-snapshot
Total syntheses of spiroviolene and spirograterpene A: a structural reassignment with biosynthetic implications
inferredcites →https://doi.org/10.1055/s-2006-956461openalex-snapshot
An Ytterbium-Catalysed Intramolecular Aldehyde-Ene Reaction Approach to the Guaianolide and Pseudoguaianolide Diterpenoids: Synthesis of the Guaiane Skeleton
inferredcites →https://doi.org/10.1070/mc1992v002n04abeh000190openalex-snapshot
Stereocontrolled Construction of the Guaiane Framework based on trans-3-lsopropenyl-2-(2’-methoxycarbonylethyl)cyclopentan-1-one
inferredcites →https://doi.org/10.1126/science.aag1028openalex-snapshot
A 15-step synthesis of (+)-ryanodol
inferredcites →https://doi.org/10.1186/s13075-019-1972-1openalex-snapshot
11β-HSD1 plays a critical role in trabecular bone loss associated with systemic glucocorticoid therapy
inferredcites →https://doi.org/10.1246/cl.1987.1485openalex-snapshot
A Mild and Convenient Method for the Reduction of Organic Halides by Using a SmI2-THF Solution in the Presence of Hexamethylphosphoric Triamide (HMPA)
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.2021.112860zenodo-depositor-declared
Terpene−Shikimate conjugated meroterpenoids from the endophytic fungus Guignardia mangiferae
inferred← citeshttps://doi.org/10.1002/ange.202104182openalex-snapshot
Enantioselective Total Syntheses of Manginoids A and C and Guignardones A and C
inferred← citeshttps://doi.org/10.1002/ange.202304033openalex-snapshot
Ketyl Radical Anion Mediated Radical Polymerization and Anionic Ring‐Opening Polymerization to Give Polymers with Low Molecular Weight Distribution
inferred← citeshttps://doi.org/10.1002/anie.202104182openalex-snapshot
Enantioselective Total Syntheses of Manginoids A and C and Guignardones A and C
inferred← citeshttps://doi.org/10.1002/anie.202304033openalex-snapshot
Ketyl Radical Anion Mediated Radical Polymerization and Anionic Ring‐Opening Polymerization to Give Polymers with Low Molecular Weight Distribution
inferred← citeshttps://doi.org/10.1002/ejoc.202500457openalex-snapshot
Decarboxylative Michael Additions of Substituted Malonic Acid Half‐Oxyesters to Methylidene Malonates
inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00137-2openalex-snapshot
Metal-Mediated Reductive C–C Coupling of π Bonds
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113289openalex-snapshot
Proposal for structural revision of several disubstituted tricycloalternarenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154361openalex-snapshot
Synthesis of the 5/6 fused-spiro tricyclic framework of manginoid A
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01895openalex-snapshot
Synthesis of the 5–6–7 Tricyclic Core of Daphnicyclidin-Type Alkaloids via a Tiffeneau–Demjanov Ring Enlargement Strategy
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02900openalex-snapshot
Rapid Construction of Tricyclic Carbon Framework for Convergent Synthesis of Manginoid Meroterpenoids
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01157openalex-snapshot
Synthesis of Desacyl Furanmonogones A and B
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03844openalex-snapshot
Soft Enolization of 3-Substituted Cycloalkanones Exhibits Significantly Improved Regiocontrol vs Hard Enolization Conditions
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.4c03643openalex-snapshot
Efforts toward the Total Synthesis of Thuggacin A
inferred← citeshttps://doi.org/10.1021/jacs.2c08760openalex-snapshot
Gram-Scale Enantioselective Synthesis of (+)-Lucidumone
inferred← citeshttps://doi.org/10.1021/jacs.2c12470openalex-snapshot
Concise Synthesis of (−)-GA 18 Methyl Ester
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/s44160-022-00046-zopenalex-snapshot
Samarium iodide-mediated C–C bond formation in the total synthesis of natural products
inferred← citeshttps://doi.org/10.1055/a-2186-7034openalex-snapshot
Examination of Diels–Alder/Tsuji–Trost Route towards Kopsia Alkaloids
inferred← citeshttps://doi.org/10.1126/sciadv.adu9264openalex-snapshot
Highly selective aldehyde coupling on the heterointerface of molybdenum selenide and graphdiyne
inferred← citeshttps://doi.org/10.1248/cpb.c21-00837openalex-snapshot
A Stereoselective Synthesis of Fused Carbocycles with a cis-1,2-Diol Moiety by Desymmetrization: SmI2-Mediated Pinacol Coupling of meso-Cyclic 1,3-Diones
inferred← citeshttps://doi.org/10.3390/ph15111392openalex-snapshot
Total Synthesis of Terpenes and Their Biological Significance: A Critical Review
inferred← citeshttps://doi.org/10.3762/bjoc.19.1openalex-snapshot
Combining the best of both worlds: radical-based divergent total synthesis
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