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An Inverse Electron Demand Diels–Alder-Based Total Synthesis of Defucogilvocarcin V and Some C-8 Analogues
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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/anie.201105882openalex-snapshot
Enzymatic Total Synthesis of Defucogilvocarcin M and Its Implications for Gilvocarcin Biosynthesis
inferredcites →https://doi.org/10.1002/ejoc.200400826openalex-snapshot
A Diels–Alder Reaction for the Total Synthesis of the Novel Antibiotic Antitumor Agent Mensacarcin
inferredcites →https://doi.org/10.1016/0006-291x(87)90320-2openalex-snapshot
Light-induced modifications of DNA by gilvocarcin V and its aglycone
inferredcites →https://doi.org/10.1016/s0040-4039(00)86100-6openalex-snapshot
Total synthesis of the aglycone of the 8-methyl benzonaphthopyrone antibiotics, gilvocarcin M, virenomycin M, and albacarcin M
inferredcites →https://doi.org/10.1016/s0040-4039(00)96148-3openalex-snapshot
Synthesis of the ravidomycin ring system
inferredcites →https://doi.org/10.1016/s0040-4039(00)96747-9openalex-snapshot
Synthesis of the glivocarcin-M aglycone
inferredcites →https://doi.org/10.1016/s0040-4039(00)97051-5openalex-snapshot
A concise total synthesis of the aglycone of the gilvocarcins
inferredcites →https://doi.org/10.1016/s0040-4039(01)93455-0openalex-snapshot
A new synthesis of defucogilvocarcin M
inferredcites →https://doi.org/10.1016/s0040-4039(96)02340-4openalex-snapshot
Electron deficient dienes I. Normal and inverse electron demand Diels-Alder reaction of the same carbon skeleton
inferredcites →https://doi.org/10.1016/s0040-4039(97)10188-5openalex-snapshot
Combined directed metalation - cross coupling strategies. Total synthesis of the aglycones of gilvocarcin V, M and E
inferredcites →https://doi.org/10.1016/s0040-4039(99)02235-2openalex-snapshot
Total synthesis of ravidomycin: revision of absolute and relative stereochemistry
inferredcites →https://doi.org/10.1021/ja00035a069openalex-snapshot
Total synthesis and absolute stereochemical assignment of gilvocarcin M.
inferredcites →https://doi.org/10.1021/ja00082a023openalex-snapshot
Total Synthesis of the Gilvocarcins
inferredcites →https://doi.org/10.1021/ja00162a046openalex-snapshot
Gilvocarcin photobiology. Isolation and characterization of the DNA photoadduct
inferredcites →https://doi.org/10.1021/jo00004a058openalex-snapshot
A strategy for the convergent synthesis of gilvocarcins via chromium carbene benzannulation. 1-O-Methyldefucogilvocarcin V in seven steps
inferredcites →https://doi.org/10.1021/jo00240a012openalex-snapshot
A concise total synthesis of defucogilvocarcin V by application of the Meyers biaryl strategy: ortho- and para-selective functionalizations of the A ring
inferredcites →https://doi.org/10.1021/jo00251a008openalex-snapshot
The photobiology of the gilvocarcins. Total synthesis of defucogilvocarcin V and a related photoactive vinyl phenol
inferredcites →https://doi.org/10.1021/jo034011xopenalex-snapshot
Enantioselective Total Synthesis of the Antitumor Macrolide Rhizoxin D
inferredcites →https://doi.org/10.1021/jo0512960openalex-snapshot
A Brief and Convergent Synthetic Route to Defucogilvocarcin M Chromophore: The Formal Synthesis of WS-5995 A and C
inferredcites →https://doi.org/10.1021/jo201775eopenalex-snapshot
Synthesis of 6H-Dibenzo[b,d]pyran-6-ones Using the Inverse Electron Demand Diels–Alder Reaction
inferredcites →https://doi.org/10.1021/jo801411popenalex-snapshot
Povarov Reactions Involving 3-Aminocoumarins: Synthesis of 1,2,3,4-Tetrahydropyrido[2,3-c]coumarins and Pyrido[2,3-c]coumarins
inferredcites →https://doi.org/10.1021/jo9001454openalex-snapshot
Combined Directed Remote Metalation−Transition Metal Catalyzed Cross Coupling Strategies: The Total Synthesis of the Aglycones of the Gilvocarcins V, M, and E and Arnottin I
inferredcites →https://doi.org/10.1021/jo990648yopenalex-snapshot
Total Synthesis of C-Glycosylangucycline, Urdamycinone B, Using an Unprotected Sugar
inferredcites →https://doi.org/10.1021/ol049261uopenalex-snapshot
Concise Three-Component Synthesis of Defucogilvocarcin M
inferredcites →https://doi.org/10.1021/ol2007428openalex-snapshot
Scope of the Inverse Electron Demand Diels–Alder Reactions of 1,2,3-Triazine
inferredcites →https://doi.org/10.1021/ol2030636openalex-snapshot
Multicomponent Synthesis of 6H-Dibenzo[b,d]pyran-6-ones and a Total Synthesis of Cannabinol
inferredcites →https://doi.org/10.1021/ol702614bopenalex-snapshot
Electron-Deficient Dienes. 5. An Inverse-Electron-Demand Diels−Alder Approach to 2-Substituted 4-Methoxyxanthones and 3,4-Dimethoxyxanthones
inferredcites →https://doi.org/10.1039/b512851jopenalex-snapshot
Model studies towards the synthesis of gilvocarcin M
inferredcites →https://doi.org/10.1039/b808633hopenalex-snapshot
Plasticity in gilvocarcin-type C-glycoside pathways: discovery and antitumoral evaluation of polycarcin V from Streptomyces polyformus
inferredcites →https://doi.org/10.1039/c2cc33611aopenalex-snapshot
Concise, aromatization-based approach to an elaborate C2-symmetric pyrenophane
inferredcites →https://doi.org/10.1039/c39870001528openalex-snapshot
Synthesis of the aglycones of the ravidomycin family of antibiotics
inferredcites →https://doi.org/10.1039/p19840001339openalex-snapshot
The acetylation of naphthoquinones. The synthesis of 3-acetyl-5-methoxy- and 3-acetyl-5,7-dimethoxy-1,4-naphthoquinones
inferredcites →https://doi.org/10.1055/s-1999-2645openalex-snapshot
Electron Deficient Dienes. 2. One Step Synthesis of a Coumarin-Fused Electron Deficient Diene and its Inverse Electron Demand Diels-Alder Reactions with Enamines
inferredcites →https://doi.org/10.1055/s-2003-36800openalex-snapshot
Electron Deficient Dienes 3:Rapid Access to 2-Hydroxybenzophenones via Inverse Electron Demand Diels-Alder-Driven Domino Reactions of a Chromone-Fused Electron Deficient Diene with Enamines
inferredcites →https://doi.org/10.1055/s-2003-38746openalex-snapshot
Electron Deficient Dienes.4.A Synthetic Equivalentof 4-Methyleneglutaconic Acid, its Mono and Diethyl Estersand their Use in a Concise General Synthesis of IsophthalicAcids and Isophthalates
inferredcites →https://doi.org/10.1111/j.1751-1097.1994.tb05095.xopenalex-snapshot
PHOTOACI'IVATED GILVOCARCIN V INDUCES DNA‐PROTEIN CROSSLINKING IN GENES FOR HUMAN RIBOSOMAL RNA AND DIHYDROFOLATE REDUCTASE
inferredcites →https://doi.org/10.1126/science.6229029openalex-snapshot
Activation of Antitumor Agent Gilvocarcins by Visible Light
inferredcites →https://doi.org/10.1128/jb.69.3.280-283.1955openalex-snapshot
CHRYSOMYCIN: A NEW ANTIBIOTIC SUBSTANCE FOR BACTERIAL VIRUSES
inferredcites →https://doi.org/10.1139/v83-058openalex-snapshot
On the structure, chemistry, and 13C nuclear magnetic resonance of ravidomycin
inferredcites →https://doi.org/10.1139/v87-072openalex-snapshot
Total synthesis of the ravidomycin aglycone (defucogilvocarcin V)
inferredcites →https://doi.org/10.1246/bcsj.54.1338openalex-snapshot
Crystal and Molecular Structure of Antibiotic Gilvocarcin M
inferredcites →https://doi.org/10.1246/bcsj.76.1675openalex-snapshot
Wittig Reaction by Using DBU as a Base
inferredcites →https://doi.org/10.3891/acta.chem.scand.53-0258openalex-snapshot
Convenient Method for the ortho-Formylation of Phenols.
inferredcites →https://doi.org/10.7164/antibiotics.34.1544openalex-snapshot
Antitumor agents from Streptomyces anandii: gilvocarcins V, M and E.
inferredcites →https://doi.org/10.7164/antibiotics.34.266openalex-snapshot
Gilvocarcins, new antitumor antibiotics. 1. Taxonomy, fermentation, isolation and biological activities.
inferredcites →https://doi.org/10.7164/antibiotics.34.271openalex-snapshot
Gilvocarcins, new antitumor antibiotics. 2. Structural elucidation.
inferredcites →https://doi.org/10.7164/antibiotics.34.701openalex-snapshot
Gilvocarcins,new antitumor antibiotics 3. Antitumor activity.
inferredcites →https://doi.org/10.7164/antibiotics.35.1038openalex-snapshot
Gilvocarcins, new antitumor antibiotics. 4. Mode of action.
inferredcites →https://doi.org/10.7164/antibiotics.35.1194openalex-snapshot
The chemistry of the antibiotics chrysomycin A and B antitumor activity of chrysomycin A.
inferredcites →https://doi.org/10.7164/antibiotics.38.1280openalex-snapshot
Defucogilvocarcin V, a new antibiotic from Streptomyces arenae 2064: Isolation, characterization, partial synthesis and biological activity.
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
inferred← citeshttps://doi.org/10.1002/9781118940228.ch3openalex-snapshot
Diels–Alder Cascades in Natural Product Total Synthesis
inferred← citeshttps://doi.org/10.1002/cssc.202401214openalex-snapshot
Green Synthesis of Alzheimer′s Disease Probes Aftobetin and Analogues Enabled by Flow Technology and Heterogeneous Photocatalysis
inferred← citeshttps://doi.org/10.1002/ejoc.201300374openalex-snapshot
Color‐Tunable Fluorescent Dyes Based on Benzo[c]coumarin
inferred← citeshttps://doi.org/10.1002/jhet.3666openalex-snapshot
Synthesis of Structurally Diversified Benzo[c]chromene Derivatives under (An)aerobic Conditions Catalyzed by CuI
inferred← citeshttps://doi.org/10.1002/tcr.202100249openalex-snapshot
Benzannulation Reactions: A Case for Perspective Change From Arene Decoration to Arene Construction
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The Diels–Alder Reaction as a Key Step in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1007/s00706-020-02586-6openalex-snapshot
Applications of Knoevenagel condensation reaction in the total synthesis of natural products
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.07.057openalex-snapshot
Biological importance of structurally diversified chromenes
inferred← citeshttps://doi.org/10.1016/j.tchem.2024.100066openalex-snapshot
Inverse electron demand Diels-Alder reaction in total synthesis of bioactive natural products
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Efficient and versatile synthesis of 5-O-acylquinic acids with a direct esterification using a p-methoxybenzyl quinate as a key intermediate
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Facile intramolecular Diels–Alder reaction of 4-(o-propargyloxy)styrylcoumarins leading to highly fluorescent coumarin-containing polycyclic compounds
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00438openalex-snapshot
Antibacterial Gilvocarcin-Type Aryl-C-Glycosides from a Soil-Derived Streptomyces Species
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03990openalex-snapshot
Asymmetric Total Synthesis of PD-116740
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02266openalex-snapshot
Cascade Lactonization/Benzannulation of Propargylamines with Dimethyl 3-Oxoglutarate for Modular Assembly of Hydroxylated/Arene-Functionalized Benzo[c]chromen-6-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03102openalex-snapshot
Carbene-Catalyzed Formal [5 + 5] Reaction for Coumarin Construction and Total Synthesis of Defucogilvocarcins
inferred← citeshttps://doi.org/10.1021/jo501565ropenalex-snapshot
V-Shaped Bis-Coumarins: Synthesis and Optical Properties
inferred← citeshttps://doi.org/10.1021/ol5031734openalex-snapshot
Boron-Selective Biaryl Coupling Approach to Versatile Dibenzoxaborins and Application to Concise Synthesis of Defucogilvocarcin M
inferred← citeshttps://doi.org/10.1039/c3ra45312jopenalex-snapshot
Dimethyl homophthalates to naphthopyrans: the total synthesis of arnottin I and the formal synthesis of (−)-arnottin II
inferred← citeshttps://doi.org/10.1039/c4cc08260eopenalex-snapshot
Rh( iii )-catalyzed oxidative C–H bond arylation with hydroquinones: sustainable synthesis of dibenzo[b,d]pyran-6-ones and benzo[d]naphtho[1,2-b]pyran-6-ones
inferred← citeshttps://doi.org/10.1039/c4tc02665aopenalex-snapshot
π-Expanded coumarins: synthesis, optical properties and applications
inferred← citeshttps://doi.org/10.1039/c6ob01701kopenalex-snapshot
A metal-free one-pot synthesis of benzo[c]chromen-6-ones from 3,4-dichlorocoumarins and butadienes using tandem photo-thermal-photo reactions
inferred← citeshttps://doi.org/10.1039/d0cc00176gopenalex-snapshot
Rh( iii )-Catalyzed sequential ortho -C–H oxidative arylation/cyclization of sulfoxonium ylides with quinones toward 2-hydroxy-dibenzo[ b,d ]pyran-6-ones
inferred← citeshttps://doi.org/10.1039/d0qo01333aopenalex-snapshot
Rhodium( iii )-catalyzed C–H activation/annulation of N -iminopyridinium ylides with alkynes and diazo compounds
inferred← citeshttps://doi.org/10.1039/d1ob02273copenalex-snapshot
Rh( iii )-catalyzed C–H annulation of sulfoxonium ylides with iodonium ylides towards isocoumarins
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Rh( iii )-catalyzed synthesis of dibenzo[ b , d ]pyran-6-ones from aryl ketone O -acetyl oximes and quinones via C–H activation and C–C bond cleavage
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Recent advances in the total synthesis of coumarin-based natural products
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Solvent free synthesis of 1-alkoxyphosphonium chlorides for stereoselective multipurpose vinyl ethers
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Regioselective Bromination: An Approach to the D-Ring of the Gilvocarcins
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