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Synthesis of 4-Acetylisocoumarin: First Total Syntheses of AGI-7 and Sescandelin
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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/jlac.199719970130openalex-snapshot
Secondary Fungal Metabolites and Their Biological Activity, VIII. – Partial Synthesis of Oosponol, an Antifungal Isocoumarin
inferredcites →https://doi.org/10.1016/s0031-9422(00)89017-2openalex-snapshot
The identification of lenzitin as oosponol
inferredcites →https://doi.org/10.1016/s0040-4039(00)94581-7openalex-snapshot
A new system for catalytic enantioselective reduction of achiral ketones to chiral alcohols. Synthesis of chiral α-hydroxy acids
inferredcites →https://doi.org/10.1021/ja00475a040openalex-snapshot
Lanthanides in organic chemistry. 1. Selective 1,2 reductions of conjugated ketones
inferredcites →https://doi.org/10.1021/jo00050a047openalex-snapshot
An improved synthesis of naphthoate precursors to olivin
inferredcites →https://doi.org/10.1021/jo00224a008openalex-snapshot
Synthesis of 4,5,9,10-tetradehydroadamantan-2-one
inferredcites →https://doi.org/10.1021/jo00445a041openalex-snapshot
Syntheses of .alpha.- and .beta.-sorigenin methyl ethers
inferredcites →https://doi.org/10.1039/p19770000702openalex-snapshot
Synthesis of doryanine and related isoquinolones and isocoumarins
inferredcites →https://doi.org/10.1055/s-1995-5132openalex-snapshot
A Short and Efficient Synthesis of 4,5-Diarylpyrimidines
inferredcites →https://doi.org/10.1248/cpb.29.2689openalex-snapshot
Antifungal activity of oosponol, oospolactone, phyllodulcin, hydrangenol, and some other related compounds.
inferredcites →https://doi.org/10.1248/cpb.31.1277openalex-snapshot
1(2H)-isoquinolones as potential antiallergic agents.
inferredcites →https://doi.org/10.1271/bbb.58.1525openalex-snapshot
Biosyntheses of Sescandelin and Sescandelin B: New Isocoumarin Compounds Produced by the Fungus,Sesquicilium candelabrum
inferredcites →https://doi.org/10.1271/bbb1961.27.817openalex-snapshot
Studies on the Metabolic Products of Oospora sp.(Oospora astringenes)
inferredcites →https://doi.org/10.1271/bbb1961.27.822openalex-snapshot
Studies on the Metabolic Products of Oospora sp, (Oospora astringenes)
inferredcites →https://doi.org/10.7164/antibiotics.54.463openalex-snapshot
Anti-angiogenic Activities of Novel Isocoumarins, AGI-7 and Sescandelin.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/047084289x.rd351.pub2openalex-snapshot
Dimethyl 2,3-Pentadienedioate
inferred← citeshttps://doi.org/10.1002/chin.200251220openalex-snapshot
Synthesis of 4‐Acetylisocoumarin: First Total Syntheses of AGI‐7 and Sescandelin.
inferred← citeshttps://doi.org/10.1002/hlca.200900348openalex-snapshot
Regioselective Synthesis of 4‐(Arylsulfanyl)‐2‐hydroxyhomophthalates by [4+2] Cycloaddition of 3‐(Arylsulfanyl)‐1‐(trimethylsilyloxy)buta‐1,3‐dienes with Dimethyl Penta‐2,3‐dienedioate
inferred← citeshttps://doi.org/10.1002/jhet.5570430510openalex-snapshot
Furan ring opening - isocoumarine ring closure: A recyclization reaction of 2-carboxyaryldifurylmethanes
inferred← citeshttps://doi.org/10.1002/slct.202201791openalex-snapshot
Total Synthesis of AGI‐7 and Sescandelin from Enol Esters
inferred← citeshttps://doi.org/10.1007/s10593-005-0303-4openalex-snapshot
2-Carboxyaryldifurylmethanes in Synthesis of Ketones in the Isocoumarin Series
inferred← citeshttps://doi.org/10.1016/b978-0-12-815411-3.00005-9openalex-snapshot
Isocoumarins in Medicinal Chemistry and Organic Synthesis
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.07.043openalex-snapshot
New DNA binding ligands as a model of chromomycin A3
inferred← citeshttps://doi.org/10.1016/j.tet.2006.05.036openalex-snapshot
Recent advances in the synthetic applications of the oxazaborolidine-mediated asymmetric reduction
inferred← citeshttps://doi.org/10.1016/j.tet.2008.05.118openalex-snapshot
Synthesis of 4-hydroxy- and 2,4-dihydroxy-homophthalates by [4+2] cycloaddition of 1,3-bis(silyloxy)-1,3-butadienes with dimethyl allene-1,3-dicarboxylate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.01.100openalex-snapshot
Efficient two directional syntheses of a homophthalate ester and novel resorcylate oligomers
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.12.024openalex-snapshot
Efficient synthesis of 1-oxo-3-aryl-1H-isochromene-4-carbaldehydes from enaminoketones of 2′-carboxamidodeoxybenzoins
inferred← citeshttps://doi.org/10.1016/s0040-4020(03)00212-6openalex-snapshot
Synthesis of 3-arylisocoumarins, including thunberginols A and B, unsymmetrical 3,4-disubstituted isocoumarins, and 3-ylidenephthalides via iodolactonization of methyl 2-ynylbenzoates or the corresponding carboxylic acids
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02602openalex-snapshot
Synthesis of Isocoumarins via Silver(I)-Mediated Annulation of Enol Esters
inferred← citeshttps://doi.org/10.1021/ar5004169openalex-snapshot
β-Keto-dioxinones and β,δ-Diketo-dioxinones in Biomimetic Resorcylate Total Synthesis
inferred← citeshttps://doi.org/10.1021/ol2011117openalex-snapshot
Synthesis and Structural Revision of Phomopsin B, a Novel Polyketide Carrying a 10-Membered Cyclic-Ether Ring
inferred← citeshttps://doi.org/10.1039/c8sc01537fopenalex-snapshot
Selective oxymetalation of terminal alkynes via 6- endo cyclization: mechanistic investigation and application to the efficient synthesis of 4-substituted isocoumarins
inferred← citeshttps://doi.org/10.1080/14786410310001620637openalex-snapshot
Biologically Active Metabolites from Fungi, 19: New Isocoumarins and Highly Substituted Benzoic Acids from the Endophytic Fungus,ScytalidiumSP.
inferred← citeshttps://doi.org/10.1080/14786410310001630555openalex-snapshot
Synthesis of 6,8-Dihydroxy-3-(2′-Acetyl-3′, 5′-Dihydroxyphenyl)Methylisocoumarin Related to Feralolide
inferred← citeshttps://doi.org/10.1107/s1600536804003034openalex-snapshot
8-Hydroxy-3,4-dimethylisocoumarin
inferred← citeshttps://doi.org/10.70675/fa3c589fz9347z4f25za191z5b6d97b4d3e1openalex-snapshot
Synthèses régiosélectives d'hétérocycles porteurs d'un groupement perfluoroalkyle
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