On the public citation graph

A Formal Synthesis of Porantheridine and an Epimer

0 signed · 102 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/anie.200200556openalex-snapshot
Recent Developments in Olefin Cross‐Metathesis
inferredcites →https://doi.org/10.1002/chem.200600813openalex-snapshot
Chiral Oxazolopiperidone Lactams: Versatile Intermediates for the Enantioselective Synthesis of Piperidine‐Containing Natural Products
inferredcites →https://doi.org/10.1002/ejoc.200400823openalex-snapshot
Recent Advances in the Total Synthesis of Piperidine Azasugars
inferredcites →https://doi.org/10.1007/bf00903333openalex-snapshot
Stereoselektive Synthese von (�)-Porantheridin und (�)-Porantherilidin
inferredcites →https://doi.org/10.1007/bf01237431openalex-snapshot
ThePoranthera corymbosa alkaloids, II. Molecular structure and absolute configuration of porantheridine hydrobromide
inferredcites →https://doi.org/10.1016/j.bmc.2007.10.018openalex-snapshot
Synthesis of pharmaceutically active compounds containing a disubstituted piperidine framework
inferredcites →https://doi.org/10.1016/j.tet.2009.07.011openalex-snapshot
Ring opening of cyclic N,O-acetals with allyltrimethylsilane under Lewis acidic conditions
inferredcites →https://doi.org/10.1016/j.tetasy.2008.01.004openalex-snapshot
Recent advances in the stereoselective synthesis of trans-3,4-disubstituted-piperidines: applications to (−)-paroxetine
inferredcites →https://doi.org/10.1016/s0040-4020(00)00159-9openalex-snapshot
New Developments in the Chemistry of N-Acyliminium Ions and Related Intermediates
inferredcites →https://doi.org/10.1016/s0040-4020(01)85590-3openalex-snapshot
Asymmetric synthesis via electrophile-mediated cyclisations
inferredcites →https://doi.org/10.1016/s0040-4020(02)00584-7openalex-snapshot
Syntheses of the sedum and related alkaloids
inferredcites →https://doi.org/10.1016/s0040-4039(00)89062-0openalex-snapshot
1,3-Aminoalcohols by reductive cleavage of isoxazolidines with molybdenum hexacarbonyl
inferredcites →https://doi.org/10.1016/s0040-4039(01)85263-1openalex-snapshot
The molecular structure and absolute configuration of Poranthericine and Porantheridine
inferredcites →https://doi.org/10.1021/cr000436xopenalex-snapshot
Gold-Catalyzed Organic Reactions
inferredcites →https://doi.org/10.1021/cr050041jopenalex-snapshot
Coinage Metal-Assisted Synthesis of Heterocycles
inferredcites →https://doi.org/10.1021/cr068434lopenalex-snapshot
Gold-Catalyzed Organic Transformations
inferredcites →https://doi.org/10.1021/cr068435dopenalex-snapshot
Alternative Synthetic Methods through New Developments in Catalysis by Gold
inferredcites →https://doi.org/10.1021/ja00072a053openalex-snapshot
Asymmetric synthesis of (-)-porantheridine
inferredcites →https://doi.org/10.1021/jo0496796openalex-snapshot
Chemoenzymatic Synthesis and Synthetic Application of Enantiopure Aminocyclopentenols: Total Synthesis of Carbocyclic (+)-Uracil Polyoxin C and Its α-Epimer
inferredcites →https://doi.org/10.1021/jo050957qopenalex-snapshot
Synthesis of 2,3-Di- and 2,3,4-Trisubstituted Furans from 1,2-Dioxines Generated by an Enyne-RCM/Diels−Alder Reaction Sequence
inferredcites →https://doi.org/10.1021/jo061340ropenalex-snapshot
Gold-Catalyzed and N-Iodosuccinimide-Mediated Cyclization of γ-Substituted Allenamides
inferredcites →https://doi.org/10.1021/jo971696qopenalex-snapshot
The Hetero Diels−Alder Reactions between d -Mannose-Derived Halonitroso Compounds and Cyclopentadiene: Scope and Limitations
inferredcites →https://doi.org/10.1021/jo972265aopenalex-snapshot
Enzymatic Resolution of Aminocyclopentenols as Precursors to d - and l -Carbocyclic Nucleosides
inferredcites →https://doi.org/10.1021/jo9906476openalex-snapshot
Efficient Total Synthesis of Enantiopure (−)-Porantheridine
inferredcites →https://doi.org/10.1021/ol0265620openalex-snapshot
A Novel C2-Symmetric 2,6-Diallylpiperidine Carboxylic Acid Methyl Ester as a Promising Chiral Building Block for Piperidine-Related Alkaloids
inferredcites →https://doi.org/10.1021/ol0474610openalex-snapshot
Total Synthesis of (+)- trans - 195A
inferredcites →https://doi.org/10.1021/ol901094hopenalex-snapshot
A Formal Synthesis of Swainsonine by Gold-Catalyzed Allene Cyclization
inferredcites →https://doi.org/10.1039/b103904kopenalex-snapshot
Nucleophilic transition metal based cyclization of allenes
inferredcites →https://doi.org/10.1039/b416516kopenalex-snapshot
The golden gate to catalysis
inferredcites →https://doi.org/10.1039/b601489eopenalex-snapshot
A new route to trans-2,6-disubstituted piperidine-related alkaloids using a novel C2-symmetric 2,6-diallylpiperidine carboxylic acid methyl ester
inferredcites →https://doi.org/10.1039/b615629kopenalex-snapshot
Gold catalysis in total synthesis
inferredcites →https://doi.org/10.1039/p19840000747openalex-snapshot
Observation on the synthesis of allenes by homologation of alk-1-ynes
inferredcites →https://doi.org/10.1055/s-1976-24157openalex-snapshot
A New Synthesis ofO-Alkylhydroxylamines
inferredcites →https://doi.org/10.1055/s-1989-27171openalex-snapshot
Formylation of Allylsilanes: A Synthesis of β,γ-Unsaturated Aldehyde Acetals
inferredcites →https://doi.org/10.1055/s-2000-8218openalex-snapshot
Stereoselective Synthesis of Piperidines
inferredcites →https://doi.org/10.1055/s-2006-941565openalex-snapshot
Asymmetric Synthesis of Hydroxylated Pyrrolidines, Piperidines and Related Bioactive Compounds: From N-Acyliminium Chemistry to N-α-Carbanion Chemistry
inferredcites →https://doi.org/10.1055/s-2008-1066985openalex-snapshot
Synthesis of Sedamine by Cycloisomerisation of an Allenic Hydroxylamine
inferredcites →https://doi.org/10.1055/s-2008-1072650openalex-snapshot
Synthesis of N,O-Heterocycles by Intramolecular Conjugate Addition of a Hydroxylamine
inferredcites →https://doi.org/10.1080/00397919808004514openalex-snapshot
A Convenient Preparation of (E)-3-Penten-2-one
inferredcites →https://doi.org/10.1246/bcsj.64.175openalex-snapshot
Synthesis of a Chiral α-(Aminooxy)arylacetic Ester. II. A Route through a Chiral 2-Hydroxy-2-phenylacetic Acid Derivative
inferredcites →https://doi.org/10.2174/1385272043370564openalex-snapshot
Recent Applications of Gold Catalysis in Organic Synthesis
inferredcites →https://doi.org/10.2174/157019308785161701openalex-snapshot
A Convenient Access to the Piperidine Ring by Cyclization of Allylsilyl Substituted N- cyliminium and Iminium Ions: Application to the Synthesis of Piperidine Alkaloids.
inferredcites →https://doi.org/10.3891/acta.chem.scand.33b-0309openalex-snapshot
Allenes and Acetylenes. XVIII. Synthesis of 3-Pyrrolines by Silver(I)-catalyzed Cyclization of Allenic Amines.

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.4460423openalex-extracted
inferred← citeshttps://doi.org/10.1002/0471264180.or088.01openalex-snapshot
Hydroamination of Alkenes
inferred← citeshttps://doi.org/10.1002/9781118342886.ch4openalex-snapshot
Golden Opportunities in the Synthesis of Natural Products and Biologically Active Compounds
inferred← citeshttps://doi.org/10.1002/9783527342822.ch3openalex-snapshot
Silver‐Catalyzed Cyclizations
inferred← citeshttps://doi.org/10.1002/9783527655588.ch15openalex-snapshot
Transition‐Metal‐Catalyzed Hydroamination Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201100160openalex-snapshot
Novel Cyclization Reactions of Aminoallenes
inferred← citeshttps://doi.org/10.1002/ajoc.201500094openalex-snapshot
Synthesis of (−)‐Deoxynupharidine by Allenic Hydroxylamine Cyclisation
inferred← citeshttps://doi.org/10.1002/ange.201101460openalex-snapshot
Allene in katalytischer asymmetrischer Synthese und Naturstoffsynthese
inferred← citeshttps://doi.org/10.1002/ange.202413892openalex-snapshot
Ni‐Catalyzed Enantioselective Reductive Cyclization/Amidation and Amination of 1,6‐Enynes and 1,7‐Enynes
inferred← citeshttps://doi.org/10.1002/anie.201101460openalex-snapshot
Allenes in Catalytic Asymmetric Synthesis and Natural Product Syntheses
inferred← citeshttps://doi.org/10.1002/anie.202413892openalex-snapshot
Ni‐Catalyzed Enantioselective Reductive Cyclization/Amidation and Amination of 1,6‐Enynes and 1,7‐Enynes
inferred← citeshttps://doi.org/10.1002/bkcs.70160openalex-snapshot
Organocatalytic asymmetric [4 + 2]‐annulation of 2‐nitroallylic alcohols with isatin‐derived ketimines: Diastereo‐ and enantioselective synthesis of spirooxindole‐1,3‐oxazinanes
inferred← citeshttps://doi.org/10.1002/chem.201102716openalex-snapshot
Stereoselective Palladium‐Catalyzed Functionalization of Homoallylic Alcohols: A Convenient Synthesis of Di‐ and Trisubstituted Isoxazolidines and β‐Amino‐δ‐Hydroxy Esters
inferred← citeshttps://doi.org/10.1002/chem.201300836openalex-snapshot
Stereodivergent Synthesis of Piperidine Alkaloids by Ring‐Rearrangement Metathesis/Reductive Lactam Alkylation of Nitroso Diels–Alder Cycloadducts
inferred← citeshttps://doi.org/10.1002/ejoc.201800526openalex-snapshot
Deoxyalkoxyamination of Alcohols for the Synthesis of N‐Alkoxy‐N‐alkylbenzenesulfonamides
inferred← citeshttps://doi.org/10.1002/ejoc.202500653openalex-snapshot
Efficient Route for Construction of Fluorinated Isoxazolines through Base‐Mediated Fluorinated Amino Acid Derivatives
inferred← citeshttps://doi.org/10.1002/vjch.201900174openalex-snapshot
The Pivotal Role of N‐O bonds in the Synthesis of Natural Products: A mini‐review
inferred← citeshttps://doi.org/10.1007/s10562-019-02746-2openalex-snapshot
Synthesis of Six-Membered N-Heterocycles Using Ruthenium Catalysts
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00008-1openalex-snapshot
1,3-Oxazines and Their Benzo Derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00135-9openalex-snapshot
Isoxazoles
inferred← citeshttps://doi.org/10.1016/b978-0-12-820282-1.00002-6openalex-snapshot
Six-membered fused N-heterocycles
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00705-7openalex-snapshot
1,3-Oxazines and their Benzo Derivatives
inferred← citeshttps://doi.org/10.1016/bs.adomc.2018.02.003openalex-snapshot
Transition Metal-Catalyzed Intramolecular Amination and Hydroamination Reactions of Allenes
inferred← citeshttps://doi.org/10.1016/bs.aihch.2019.06.001openalex-snapshot
1,3-Amino alcohols and their phenol analogs in heterocyclization reactions
inferred← citeshttps://doi.org/10.1016/bs.alkal.2014.12.001openalex-snapshot
Simple Indolizidine and Quinolizidine Alkaloids
inferred← citeshttps://doi.org/10.1016/bs.alkal.2022.06.001openalex-snapshot
The biological activities of quinolizidine alkaloids
inferred← citeshttps://doi.org/10.1016/j.tet.2011.07.087openalex-snapshot
Applications of allylamines for the syntheses of aza-heterocycles
inferred← citeshttps://doi.org/10.1016/j.tet.2012.05.125openalex-snapshot
Transition metal-catalyzed addition of C-, N- and O-nucleophiles to unactivated C–C multiple bonds
inferred← citeshttps://doi.org/10.1016/j.tet.2014.02.001openalex-snapshot
A synthesis of 5-hydroxysedamine using hydroformylation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.12.026openalex-snapshot
Synthesis of the sedum and related alkaloids: A personal perspective
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154614openalex-snapshot
A novel approach towards the synthesis of an oxazine scaffold using scandium trifluoromethanesulfonate catalysed N, O-acetal and olefin cyclisation sequence
inferred← citeshttps://doi.org/10.1021/acs.accounts.0c00806openalex-snapshot
The Development of Reaction Cascades to Synthesize Dimeric Coccinellid Alkaloids
inferred← citeshttps://doi.org/10.1021/acs.accounts.4c00462openalex-snapshot
Hydroxylamines: From Synthetic Intermediates to Synthetic Targets
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00543openalex-snapshot
Isoxazolidine: A Privileged Scaffold for Organic and Medicinal Chemistry
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.1c02070openalex-snapshot
Construction of Stable Metal–Organic Framework Platforms Embedding N -Heterocyclic Carbene Metal Complexes for Selective Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02469openalex-snapshot
Chiroptical Protocol for the Absolute Configurational Assignment of Alkyl-Substituted Epoxides Using Bis(zinc porphyrin) as a CD-Sensitive Bidentate Host
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02461openalex-snapshot
Identification of a Grain Beetle Macrolide Pheromone and Its Synthesis by Ring-Closing Metathesis Using a Terminal Alkyne
inferred← citeshttps://doi.org/10.1021/acscatal.5b01061openalex-snapshot
Gold-Catalyzed Reactivity Reversal of Indolizidinone-Tethered β-Amino Allenes Controlled by the Stereochemistry
inferred← citeshttps://doi.org/10.1021/cr300389uopenalex-snapshot
Late Transition Metal-Catalyzed Hydroamination and Hydroamidation
inferred← citeshttps://doi.org/10.1021/jacs.2c03620openalex-snapshot
Palladium-Catalyzed Asymmetric Sequential Hydroamination of 1,3-Enynes: Enantioselective Syntheses of Chiral Imidazolidinones
inferred← citeshttps://doi.org/10.1021/jo100768dopenalex-snapshot
Synthetic Approaches to Racemic Porantheridine and 8-Epihalosaline via a Nitroso Diels−Alder Cycloaddition/Ring-Rearrangement Metathesis Sequence
inferred← citeshttps://doi.org/10.1021/jo101346topenalex-snapshot
Ring-Opening Polymerization of ε-Caprolactone Catalyzed by Sulfonic Acids: Computational Evidence for Bifunctional Activation
inferred← citeshttps://doi.org/10.1021/jo400760qopenalex-snapshot
Asymmetric Total Synthesis of Fusarentin 6-Methyl Ether and Its Biomimetic Transformation into Fusarentin 6,7-Dimethyl Ether, 7-O-Demethylmonocerin, and (+)-Monocerin
inferred← citeshttps://doi.org/10.1021/jo401627popenalex-snapshot
FeCl3·6H2O, a Catalyst for the Diastereoselective Synthesis of cis-Isoxazolidines from N-Protected δ-Hydroxylamino Allylic Acetates
inferred← citeshttps://doi.org/10.1021/ma101461yopenalex-snapshot
Ring-Opening Polymerization of Trimethylene Carbonate Catalyzed by Methanesulfonic Acid: Activated Monomer versus Active Chain End Mechanisms
inferred← citeshttps://doi.org/10.1021/ol1016492openalex-snapshot
Synthesis of (−)-Sedinine by Allene Cyclization and Iminium Ion Chemistry
inferred← citeshttps://doi.org/10.1021/ol101651topenalex-snapshot
Direct Enantioselective Brønsted Acid Catalyzed N-Acyliminium Cyclization Cascades of Tryptamines and Ketoacids
inferred← citeshttps://doi.org/10.1021/ol202796wopenalex-snapshot
Diastereoselective Access to Nonracemic 2-cis-Substituted and 2,6-cis-Disubstituted Piperidines
inferred← citeshttps://doi.org/10.1039/c1cs15279copenalex-snapshot
Gold catalysis in total synthesis—an update
inferred← citeshttps://doi.org/10.1039/c2ob07107jopenalex-snapshot
Aminohydroxyacetone synthons: versatile intermediates for the organocatalytic asymmetric aldol reaction
inferred← citeshttps://doi.org/10.1039/c3cs60408jopenalex-snapshot
Silver and platinum-catalysed addition of O–H and N–H bonds to allenes
inferred← citeshttps://doi.org/10.1039/c4ob00537fopenalex-snapshot
A total synthesis of (+)-negamycin through isoxazolidine allylation
inferred← citeshttps://doi.org/10.1039/c6nj00980hopenalex-snapshot
Room temperature hydroamination of alkynes with anilines catalyzed by anti-Bredt di(amino)carbene gold( i ) complexes
inferred← citeshttps://doi.org/10.1039/c8qo01398eopenalex-snapshot
A unified and straightforward total synthesis of (+)-porantheridine and (−)-6- epi -porantheridine
inferred← citeshttps://doi.org/10.1039/d5qo01747eopenalex-snapshot
Flow chemistry-assisted visible light-induced radical addition of β-amino iodides with enones en route to efficient construction of cis -2,6-piperidines
inferred← citeshttps://doi.org/10.1055/a-1381-2881openalex-snapshot
Chemical Diversity of Volatile Macrocylic Lactones from Frogs
inferred← citeshttps://doi.org/10.1055/sos-sd-221-00172openalex-snapshot
1.6 Metal-Catalyzed Cyclization Reactions of Allenes
inferred← citeshttps://doi.org/10.1201/9781351242615-9openalex-snapshot
Six-Membered Fused N-Heterocycles
inferred← citeshttps://doi.org/10.70675/df877f77z5ffaz4bfcz9e52z3bb0e678aba9openalex-snapshot
Studies towards the synthesis of bioactive natural products and development of new synthetic methods
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.