On the public citation graph
Copper-Catalyzed Cyclization of Steroidal Acylaminoacetylenes: Syntheses of Novel 11β-Aryl-17,17- spiro[(4‘ H ,5‘-methylene)oxazol]-Substituted Steroids
0 signed · 63 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1099-0690(199804)1998:4<679::aid-ejoc679>3.0.co;2-wopenalex-snapshot
Zirconium-Catalyzed Oxidation of Primary Aliphatic Amines to Nitro Compounds withtert-Butyl Hydroperoxide
inferredcites →https://doi.org/10.1002/chin.200408098openalex-snapshot
2‐Aryl and 2‐Heteroaryl Indoles from 1‐Alkynes and o‐Iodotrifluoroacetanilide Through a Domino Copper‐Catalyzed Coupling—Cyclization Process.
inferredcites →https://doi.org/10.1016/0022-4731(87)90159-2openalex-snapshot
Synthesis of antiprogestational steroids
inferredcites →https://doi.org/10.1016/0022-4731(89)90118-0openalex-snapshot
New analogues of mifepristone with more dissociated antiprogesterone activities
inferredcites →https://doi.org/10.1016/0024-3205(93)90135-popenalex-snapshot
Reversal of activity profile in analogs of the antiprogestin RU 486: Effect of a 16α-substituent on progestational (agonist) activity
inferredcites →https://doi.org/10.1016/0039-128x(94)90040-xopenalex-snapshot
Synthesis of a fluorescent steroid derivative with high affinities for the glucocorticoid and progesterone receptors
inferredcites →https://doi.org/10.1016/j.steroids.2003.08.007openalex-snapshot
Progesterone antagonists and progesterone receptor modulators: an overview
inferredcites →https://doi.org/10.1016/s0039-128x(00)00189-6openalex-snapshot
Preclinical experience with two selective progesterone receptor modulators on breast and endometrium
inferredcites →https://doi.org/10.1021/ja00354a023openalex-snapshot
(.eta.5-Cyclopentadienyl)- and (.eta.5-pentamethylcyclopentadienyl)copper compounds containing phosphine, carbonyl, and .eta.2-acetylenic ligands
inferredcites →https://doi.org/10.1021/jo00137a008openalex-snapshot
Reductive cleavage of hydroxylamine derivatives by dihydrolipoic acid-iron(II)
inferredcites →https://doi.org/10.1021/jo01058a016openalex-snapshot
The Synthesis of 17β-Amino-17α-(2'-carboxyethyl)androstane Lactams1
inferredcites →https://doi.org/10.1021/jo0200217openalex-snapshot
Efficient and General Synthesis of 5-(Alkoxycarbonyl)methylene-3-oxazolines by Palladium-Catalyzed Oxidative Carbonylation of Prop-2-ynylamides
inferredcites →https://doi.org/10.1021/jo0357770openalex-snapshot
Synthesis of 4H-3,1-Benzoxazines, Quinazolin-2-ones, and Quinoline-4-ones by Palladium-Catalyzed Oxidative Carbonylation of 2-Ethynylaniline Derivatives
inferredcites →https://doi.org/10.1021/ol035378ropenalex-snapshot
2-Aryl and 2-Heteroaryl Indoles from 1-Alkynes ando-Iodotrifluoroacetanilide through a Domino Copper-Catalyzed Coupling−Cyclization Process
inferredcites →https://doi.org/10.1039/p19890000333openalex-snapshot
The α-alk-1-ynylation of β-dicarbonyl compounds and nitronate salts by alk-1-ynyl-lead triacetates
inferredcites →https://doi.org/10.1055/s-1977-24574openalex-snapshot
A Convenient Synthesis of 1-Alkynyl Ketones and 2-Alkynamides
inferredcites →https://doi.org/10.1093/humrep/9.suppl_1.12openalex-snapshot
History and perspectives of antiprogestins from the chemist's point of view
inferredcites →https://doi.org/10.1093/humrep/9.suppl_1.32openalex-snapshot
Effects of D-ring substituents on antiprogestational (antagonist) and progestational (agonist) activity of 11 -aryl steroids
inferredcites →https://doi.org/10.1093/humupd/dmi002openalex-snapshot
Selective progesterone receptor modulators and progesterone antagonists: mechanisms of action and clinical applications
inferredcites →https://doi.org/10.1111/j.1749-6632.1995.tb31379.xopenalex-snapshot
Pharmacological Properties of a New Selective Antiprogestagen: Org 33628
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4781830openalex-extracted
Novel Steroidal Spiro-Heterocycles Via One-Step Cyclocondensation Reactions. Evaluation as Antiproliferative Agents
inferred← citeshttps://doi.org/10.1002/adsc.201400144openalex-snapshot
Transition Metal‐Free Trifluoromethylation of N ‐Allylamides with Sodium Trifluoromethanesulfinate: Synthesis of Trifluoromethyl‐Containing Oxazolines
inferred← citeshttps://doi.org/10.1002/adsc.201500610openalex-snapshot
Silver‐Catalyzed Cyclization of Propargylic Amides to Oxazolines
inferred← citeshttps://doi.org/10.1002/adsc.201900264openalex-snapshot
Gold‐Catalyzed Stereoselective Domino Cyclization/Alkynylation of N‐Propargylcarboxamides with Benziodoxole Reagents for the Synthesis of Alkynyloxazolines
inferred← citeshttps://doi.org/10.1002/ange.201303684openalex-snapshot
Carbonylation of Propargyl Carbamates with Palladium(II) Bisoxazoline Catalysts: Efficient Synthesis of 5‐Methoxy‐3(2H)‐furanones
inferred← citeshttps://doi.org/10.1002/ange.202012678openalex-snapshot
Asymmetric Allylation by Chiral Organocatalyst‐Promoted Formal Hetero‐Ene Reactions of Alkylgold Intermediates
inferred← citeshttps://doi.org/10.1002/anie.201303684openalex-snapshot
Carbonylation of Propargyl Carbamates with Palladium(II) Bisoxazoline Catalysts: Efficient Synthesis of 5‐Methoxy‐3(2H)‐furanones
inferred← citeshttps://doi.org/10.1002/anie.202012678openalex-snapshot
Asymmetric Allylation by Chiral Organocatalyst‐Promoted Formal Hetero‐Ene Reactions of Alkylgold Intermediates
inferred← citeshttps://doi.org/10.1002/chem.201001539openalex-snapshot
Ethynyl‐1,2‐benziodoxol‐3(1 H)‐one (EBX): An Exceptional Reagent for the Ethynylation of Keto, Cyano, and Nitro Esters
inferred← citeshttps://doi.org/10.1002/chin.200738179openalex-snapshot
Copper‐Catalyzed Cyclization of Steroidal Acylaminoacetylenes: Syntheses of Novel 11β‐Aryl‐17,17‐spiro[(4′H,5′‐methylene)oxazol]‐Substituted Steroids.
inferred← citeshttps://doi.org/10.1002/cptc.202000239openalex-snapshot
Preparation of Oxazole Acetals from N‐Propargylamides Enabled by Visible‐Light‐Promoted Selenium‐π‐Acid Catalysis
inferred← citeshttps://doi.org/10.1002/ejoc.201100342openalex-snapshot
Gold‐Catalyzed Cyclization of Nonterminal Propargylic Amides to Substituted Alkylideneoxazolines and ‐oxazines
inferred← citeshttps://doi.org/10.1002/ejoc.201300719openalex-snapshot
An Efficient Approach to Azolyl‐Substituted Steroids through Copper‐Catalyzed Ullmann C–N Coupling
inferred← citeshttps://doi.org/10.1002/ejoc.201301511openalex-snapshot
High‐Pressure‐Mediated Extension of the Privileged Steroid Scaffold
inferred← citeshttps://doi.org/10.1002/slct.202403170openalex-snapshot
Development of Steroidal Spiro‐Heterocycles Through One‐Step Cyclocondensation, Their Evaluation as Antiproliferative Agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.08.064openalex-snapshot
Synthesis and identification of novel 11β-aryl-4′,5′-dihydrospiro[estra-4,9-diene-17β,4′-oxazole] analogs with dissociated antiprogesterone activities
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.12.110openalex-snapshot
Synthesis and antihormonal properties of novel 11β-benzoxazole-substituted steroids
inferred← citeshttps://doi.org/10.1016/j.mcat.2018.03.015openalex-snapshot
Palladium-catalysed aminocarbonylation/cyclization of iodoalkenes toward N-propargylcarboxamides and oxazoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.02.077openalex-snapshot
4-Picoline-catalyzed hetero-Diels–Alder type reactions: one-pot synthesis of pyrano[4,3-c]chromenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.11.061openalex-snapshot
Cyclization reactions of propargylic amides: mild access to N-heterocycles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.10.043openalex-snapshot
Copper-catalyzed hydroamination of propargyl imidates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.02.058openalex-snapshot
A facile one-pot synthesis of 2- o -cyanoaryl oxazole derivatives mediated by CuCN
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00171openalex-snapshot
Site-Selective Double and Tetracyclization Routes to Fused Polyheterocyclic Structures by Pd-Catalyzed Carbonylation Reactions
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01860openalex-snapshot
Utilization of Copper-Catalyzed Carboarylation–Ring Closure for the Synthesis of New Oxazoline Derivatives
inferred← citeshttps://doi.org/10.1021/jacs.7b00892openalex-snapshot
Palladium(II)-Catalyzed Directed anti- Hydrochlorination of Unactivated Alkynes with HCl
inferred← citeshttps://doi.org/10.1021/jo301288wopenalex-snapshot
From Propargylic Amides to Functionalized Oxazoles: Domino Gold Catalysis/Oxidation by Dioxygen
inferred← citeshttps://doi.org/10.1021/jo402670dopenalex-snapshot
Cu(I)-Catalyzed Synthesis of Dihydropyrimidin-4-ones toward the Preparation of β- and β3-Amino Acid Analogues
inferred← citeshttps://doi.org/10.1021/jo5001719openalex-snapshot
From Propargylamides to Oxazole Derivatives: NIS-Mediated Cyclization and Further Oxidation by Dioxygen
inferred← citeshttps://doi.org/10.1021/jo900425wopenalex-snapshot
Development of a Diversity-Oriented Approach to Oxazole-5-amide Libraries
inferred← citeshttps://doi.org/10.1021/ol301980gopenalex-snapshot
Facile, Selective, and Regiocontrolled Synthesis of Oxazolines and Oxazoles Mediated by ZnI2 and FeCl3
inferred← citeshttps://doi.org/10.1021/ol302031zopenalex-snapshot
Catalyst-Free Intramolecular Oxidative Cyclization of N-Allylbenzamides: A New Route to 2,5-Substituted Oxazoles
inferred← citeshttps://doi.org/10.1021/op300084zopenalex-snapshot
A Flow-Based Synthesis of 2-Aminoadamantane-2-carboxylic Acid
inferred← citeshttps://doi.org/10.1039/c1ob05512gopenalex-snapshot
Tungsten and molybdenum catalyst-mediated cyclisation of N-propargyl amides
inferred← citeshttps://doi.org/10.1039/c3ob42030bopenalex-snapshot
CuI-catalyzed cycloisomerization of propargyl amides
inferred← citeshttps://doi.org/10.1039/c3ra47603kopenalex-snapshot
Solar photo-thermochemical syntheses of 4-bromo-2,5-substituted oxazoles from N-arylethylamides
inferred← citeshttps://doi.org/10.1039/c4sc02331eopenalex-snapshot
Divergent regioselectivity in photoredox-catalyzed hydrofunctionalization reactions of unsaturated amides and thioamides
inferred← citeshttps://doi.org/10.1039/c6nj03276aopenalex-snapshot
Facile syntheses of N-heterocyclic carbene precursors through Cu( ii )- or Ag( i )-catalyzed amination of N-alkynyl formamidines
inferred← citeshttps://doi.org/10.1039/c6ra25857copenalex-snapshot
Readily switchable one-pot 5-exo-dig cyclization using a palladium catalyst
inferred← citeshttps://doi.org/10.1039/c8ob01474dopenalex-snapshot
Preparation of oxazolines and oxazoles via a PhI(OAc) 2 -promoted cyclization of N -propargylamides
inferred← citeshttps://doi.org/10.1039/c8py01110aopenalex-snapshot
Peroxynitrite-biosignal-responsive polymer micelles as intracellular hypersensitive nanoprobes
inferred← citeshttps://doi.org/10.3184/174751914x13899480812215openalex-snapshot
An Efficient Synthesis of Novel Dihydrothiazol-2-yl-amides via Cyclisation of Propargylic Carbamothioyl-amides
inferred← citeshttps://doi.org/10.3390/m1233openalex-snapshot
(E)-4-Oxo-3,4-dihydroquinazoline-2-carbaldehyde Oxime
inferred← citeshttps://doi.org/10.3762/bjoc.20.152openalex-snapshot
Syntheses and medicinal chemistry of spiro heterocyclic steroids
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.