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Stereo-controlled synthesis of dl-prostaglandins F2.alpha. and E2
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inferred← citeshttps://doi.org/10.1002/hlca.19750580521openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hlca.19770600404openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hlca.19820650202openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hlca.19830660127openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hlca.19830660629openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hlca.19940770710openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hlca.200490189openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hlca.201300191openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hlca.202500009openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlac.198419840412openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlac.198519851106openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlac.198719870328openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlac.199419940302openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlac.199419940303openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlcr.2580140406openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlcr.2580190405openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlcr.2580220209openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlcr.544openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jps.2600680712openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jps.2600750322openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/mrc.1260301120openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/mrc.1270110509openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/nadc.19820300707openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/prac.19843260421openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/prac.19873290610openalex-snapshot
Construction of the Alkyl Side Chain of 11‐Deoxyprostaglandins Using the Aldol Reaction of Substituted Cyclopentane Carbaldehydes with Heptan‐2‐one
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The diastereofacial selectivity of the addition of various 1‐metalated 1‐heptynes to substituted cyclopentanecarbaldehydes. – The use of 1‐titanated 1‐heptyne for the construction of the alkyl side chain of Prostaglandins
inferred← citeshttps://doi.org/10.1002/recl.19700891006openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/recl.19770961008openalex-snapshot
Synthesis of 9,11‐dideoxy‐9a‐homoprostaglandins
inferred← citeshttps://doi.org/10.1002/recl.19831020504openalex-snapshot
Synthesis of 10,10‐dimethylprostaglandin F1 and F2 analogues
inferred← citeshttps://doi.org/10.1002/recl.19921111103openalex-snapshot
Reactions of alkenoic acids with sulfur trioxide; sulfonation and sulfo‐lactonization
inferred← citeshttps://doi.org/10.1002/recl.19931120402openalex-snapshot
Intramolecular competition in Friedel‐Crafts sulfocyclization of ω‐(1‐naphthyl)‐n‐alkenes and 1,7‐diphenyl‐3‐heptene on reaction with sulfur trioxide
inferred← citeshttps://doi.org/10.1002/tcr.201100043openalex-snapshot
Artificial Metalloenzymes as Catalysts in Stereoselective Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1002/tcr.201200010openalex-snapshot
Applications of Helical‐Chiral Pyridines as Organocatalysts in Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1002/tcr.202000054openalex-snapshot
Prostaglandin Total Synthesis Enabled by the Organocatalytic Dimerization of Succinaldehyde
inferred← citeshttps://doi.org/10.1002/zfch.19790191212openalex-snapshot
Synthese eines Zwischenprodukts für 8‐Methyl‐prostaglandin C2
inferred← citeshttps://doi.org/10.1002/zfch.19820220516openalex-snapshot
Mikrobielle Transformation von Chorhaeptan‐2‐on; Vorläufige Ergebnisse zur Darstellung eines chiralen Phosphoniumsalzes für Prostaglandinsynthesen
inferred← citeshttps://doi.org/10.1007/978-1-4613-8327-7_6openalex-snapshot
Asymmetric Carbon-Heteroatom Bond Formations
inferred← citeshttps://doi.org/10.1007/978-1-4684-2778-3_2openalex-snapshot
Some Synthetic Aspects of Prostaglandins
inferred← citeshttps://doi.org/10.1007/978-1-4899-3420-8_5openalex-snapshot
Miscellaneous Natural Products
inferred← citeshttps://doi.org/10.1007/978-1-4899-3422-2_5openalex-snapshot
Miscellaneous Natural Products
inferred← citeshttps://doi.org/10.1007/978-3-032-09901-3_1openalex-snapshot
The Diels–Alder Reaction as a Key Step in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1007/978-3-322-94015-5_8openalex-snapshot
Baeyer-Villiger-Oxidation
inferred← citeshttps://doi.org/10.1007/978-3-322-94077-3_8openalex-snapshot
Baeyer-Villiger-Oxidation
inferred← citeshttps://doi.org/10.1007/978-3-322-94726-0_8openalex-snapshot
Baeyer-Villiger-Oxidation
inferred← citeshttps://doi.org/10.1007/978-3-540-30429-6_49openalex-snapshot
Carbasugars: Synthesis and Functions
inferred← citeshttps://doi.org/10.1007/978-3-642-56874-9_63openalex-snapshot
Carbasugars: Synthesis and Functions
inferred← citeshttps://doi.org/10.1007/978-3-642-58261-5_16openalex-snapshot
Asymmetrische Totalsynthesen von Prostaglandin F2α und Compactin
inferred← citeshttps://doi.org/10.1007/978-3-642-68558-3_11openalex-snapshot
Spezielle Syntheseplanungssysteme mittels Computer
inferred← citeshttps://doi.org/10.1007/978-3-7091-7123-3_7openalex-snapshot
Total Synthesis of Prostaglandins
inferred← citeshttps://doi.org/10.1007/978-94-010-9697-3_9openalex-snapshot
The Chemistry of the Prostaglandins
inferred← citeshttps://doi.org/10.1007/978-94-011-0235-3_4openalex-snapshot
Asymmetric Carbon-Hetero Bond Formations
inferred← citeshttps://doi.org/10.1007/bf00953707openalex-snapshot
Synthesis of 5-bromopentanoic acid through catalytic decomposition of the hydroperoxides of cyclopentanone
inferred← citeshttps://doi.org/10.1007/bf02290615openalex-snapshot
Stereoselective synthesis of 2e-phenyl-4e-hydroxy-1-azaspiro[5.5]undecane
inferred← citeshttps://doi.org/10.1007/bf02471884openalex-snapshot
Prostanoids, part LXX. Synthesis and study of antiinflammatory and antiulcerogenic activity of 2-(3-hydroxy-1e-octenyl)phenylacetic acid methyl ester
inferred← citeshttps://doi.org/10.1007/bf02975303openalex-snapshot
Synthesis of new prostaglandin F2α derivatives
inferred← citeshttps://doi.org/10.1007/bfb0018057openalex-snapshot
Selected topics of the wittig reaction in the synthesis of natural products
inferred← citeshttps://doi.org/10.1007/bfb0048449openalex-snapshot
Syntheses and activity of heteroprostanoids
inferred← citeshttps://doi.org/10.1007/s11172-023-4026-4openalex-snapshot
Some aspects of the synthesis and modification of cross-conjugated cyclopentenone prostaglandins
inferred← citeshttps://doi.org/10.1007/s44371-025-00422-6openalex-snapshot
Design, synthesis, and reactivity study of (3-(4-bromophenyl)isoxazole-5-yl)methanol with isobutyric acid
inferred← citeshttps://doi.org/10.1016/0003-2697(73)90373-4openalex-snapshot
Methods for quantitative analysis of PGF2α, PGE2, 9α,11α-dihydroxy-15-keto-prost-5-enoic acid and 9α,11α,15-trihydroxy-prost-5-enoic acid from body fluids using deuterated carriers and gas chromatography-mass spectrometry
inferred← citeshttps://doi.org/10.1016/0006-291x(71)90850-3openalex-snapshot
Mass spectrometric determination of picomole amounts of prostaglandins E2 and F2α using synthetic deuterium labeled carriers
inferred← citeshttps://doi.org/10.1016/0009-3084(88)90139-9openalex-snapshot
Cyclic fatty acid monomers: synthesis and characterization of methyl ω-(2-alkylcyclopentyl) alkenoates and alkanoates
inferred← citeshttps://doi.org/10.1016/0040-4020(76)85163-0openalex-snapshot
Prostaglandin chemistry—V
inferred← citeshttps://doi.org/10.1016/0040-4020(77)80400-6openalex-snapshot
Prostaglandin chemistry—VIII
inferred← citeshttps://doi.org/10.1016/0040-4020(79)80130-1openalex-snapshot
A survey of novel and useful reactions discovered through research on prostaglandins
inferred← citeshttps://doi.org/10.1016/0040-4020(80)80111-6openalex-snapshot
Steric control in prostaglandin synthesis involving bicyclic and tricyclic intermediates
inferred← citeshttps://doi.org/10.1016/0040-4020(80)80135-9openalex-snapshot
Synthetic methods using α-heterosubstituted organometallics
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