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New Crinine-Type Alkaloids with Inhibitory Effect on Induction of Inducible Nitric Oxide Synthase from Crinum yemense

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What this work says

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

inferredcites →https://doi.org/10.1016/s0099-9598(08)60186-8openalex-snapshot

Chapter 1 Antitumor Alkaloids

inferredcites →https://doi.org/10.1016/s0099-9598(08)60208-4openalex-snapshot

Chapter 3 The Amaryllidaceae Alkaloids

inferredcites →https://doi.org/10.1016/s0960-894x(01)00413-9openalex-snapshot

Absolute stereostructures of novel norcadinane- and trinoreudesmane-type sesquiterpenes with nitric oxide production inhibitory activity from Alpinia oxyphylla

inferredcites →https://doi.org/10.1016/s0960-894x(99)00702-7openalex-snapshot

Effects of stilbene constituents from rhubarb on nitric oxide production in lipopolysaccharide-activated macrophages

inferredcites →https://doi.org/10.1016/s0968-0896(01)00093-1openalex-snapshot

Inhibitors from Rhubarb on Lipopolysaccharide-Induced Nitric Oxide Production in Macrophages: Structural Requirements of Stilbenes for the Activity

inferredcites →https://doi.org/10.1021/np020078oopenalex-snapshot

Absolute Stereostructures of Three New Sesquiterpenes from the Fruit of Alpinia oxyphylla with Inhibitory Effects on Nitric Oxide Production and Degranulation in RBL-2H3 Cells

inferredcites →https://doi.org/10.1055/s-2006-957781openalex-snapshot

Alkaloids fromNarcissus asturiensis

inferredcites →https://doi.org/10.3987/com-03-9804openalex-snapshot

(7R,8S) and (7S,8R) 8-5' Linked Neolignans from Egyptian Herbal Medicine Anastatica hierochuntica and Inhibitory Activities of Lignans on Nitric Oxide Production

inferredcites →https://doi.org/10.3987/com-97-7878openalex-snapshot

Crude Drugs from Aquatic Plants. VI. On the Alkaloid Constituents of Chinese Nupharis Rhizoma, the Dried Rhizoma of Nuphar pumilum (TIMM.) DC. (Nymphaceae): Structures and Rearrangement Reaction of Thiohemiaminal Type Nuphar Alkaloids

inferredcites →https://doi.org/10.3987/com-97-s15openalex-snapshot

Crude Drugs from Aquatic Plants. VII. Four New Thiaspirane Sulfoxide Type Nuphar Alkaloids, Nupharpumilamines A, B, C, and D, from Chinese Nupharis Rhizoma, the Rhizoma of Nuphar pumilum (TIMM.) DC. (Nymphaceae)

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112485zenodo-depositor-declared

Streamlined targeting of Amaryllidaceae alkaloids from the bulbs of Crinum scillifolium using spectrometric and taxonomically-informed scoring metabolite annotations

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113473zenodo-depositor-declared

Alkaloids with cholinesterase inhibitory activities from the bulbs of Crinum × amabile Donn ex Ker Gawl

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Palladium‐Catalyzed Oxidative CC Bond Cleavage Cyclization of Biaryl‐2‐amines with Alkenes Involving CH Olefination and Carboamination

inferred← citeshttps://doi.org/10.1002/adsc.201400660openalex-snapshot

Di‐tert Butyl Peroxide‐Promoted Sequential Methylation and Intramolecular Aromatization of Isonitriles

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Palladium‐Catalyzed Synthesis of 6H‐Dibenzo[c,h]chromenes and 5,6‐Dihydrobenzo[c]phenanthridines: Application to the Synthesis of Dibenzo[c,h]chromene‐6‐ones, Benzo[c]phenanthridines, and Arnottin I

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Unprecedented Reactivity of AgSCF3 with o‐Isocyanobiaryls: Synthetic and Mechanistic Insight

inferred← citeshttps://doi.org/10.1002/ajoc.202300369openalex-snapshot

Recent Advancements in Synthesis of Phenanthridines via 2‐Isocyanobiphenyls

inferred← citeshttps://doi.org/10.1002/ajoc.70299openalex-snapshot

mpg‐CN Photo‐Catalyzed Annulation of 2‑Isocyanobiaryls With Silanes to 6‑Silyl‐Substituted Phenanthridines

inferred← citeshttps://doi.org/10.1002/ange.201306082openalex-snapshot

6‐Trifluoromethyl‐Phenanthridines through Radical Trifluoromethylation of Isonitriles

inferred← citeshttps://doi.org/10.1002/ange.201308376openalex-snapshot

Synthesis of 6‐Alkylated Phenanthridine Derivatives Using Photoredox Neutral Somophilic Isocyanide Insertion

inferred← citeshttps://doi.org/10.1002/anie.201306082openalex-snapshot

6‐Trifluoromethyl‐Phenanthridines through Radical Trifluoromethylation of Isonitriles

inferred← citeshttps://doi.org/10.1002/anie.201308376openalex-snapshot

Synthesis of 6‐Alkylated Phenanthridine Derivatives Using Photoredox Neutral Somophilic Isocyanide Insertion

inferred← citeshttps://doi.org/10.1002/asia.202200088openalex-snapshot

Silver‐catalyzed Radical Cascade Arylthiodifluoromethylation/ Cyclization of Isonitriles for the Synthesis of 6‐Phenanthridinyldifluoromethyl Aryl Thioethers

inferred← citeshttps://doi.org/10.1002/asia.202400176openalex-snapshot

Electro‐oxidative Methylation of 2‐Isocyanobiaryls Using N,N‐dimethylformamide (DMF) as Carbon Source: Synthesis of 6‐Methylphenanthridines

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Exploring the Anti‐Inflammatory Potential of Australian Native Plants Based on their Ethnopharmacological Knowledge

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Palladium‐Catalyzed Synthesis of Phenanthridine/Benzoxazine‐Fused Quinazolinones by Intramolecular CH Bond Activation

inferred← citeshttps://doi.org/10.1002/chem.201504186openalex-snapshot

Regioselective Synthesis of Quinazolinone‐/Phenanthridine‐Fused Heteropolycycles by Pd‐Catalyzed Direct Intramolecular Aerobic Oxidative C−H Amination from Aromatic Strained Amides

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Divergent Construction of N‐Doped Polycyclic Aromatic Hydrocarbons with Indole as the Nitrogen Source Building Block

inferred← citeshttps://doi.org/10.1002/chir.22719openalex-snapshot

Amaryllidaceae alkaloids: Absolute configuration and biological activity

inferred← citeshttps://doi.org/10.1002/cjoc.202400628openalex-snapshot

Photochemical Decarboxylative Radical Alkylation/Cyclization Reaction to Fused Nitrogen Heterocycles by LiI / PPh3 Catalysis

inferred← citeshttps://doi.org/10.1002/cmdc.201100608openalex-snapshot

Bulbispermine: A Crinine‐Type Amaryllidaceae Alkaloid Exhibiting Cytostatic Activity toward Apoptosis‐Resistant Glioma Cells

inferred← citeshttps://doi.org/10.1002/ejoc.201402913openalex-snapshot

Synthesis of 6‐Substituted Phenanthridine Derivatives by Palladium‐Catalysed Domino Suzuki–Miyaura/Aza‐Michael Reactions

inferred← citeshttps://doi.org/10.1002/ejoc.201500988openalex-snapshot

Preparation of 6‐Difluoromethylphosphonated Phenanthridines by Visible‐Light‐Driven Radical Cyclization of 2‐Isocyanobiphenyls

inferred← citeshttps://doi.org/10.1002/ejoc.201700185openalex-snapshot

Organocatalytic Enantioselective Synthesis of 6‐Aryl‐5,6‐dihydrophenanthridines by a Modified Pictet–Spengler Reaction of Biphenyl‐2‐amines and Aromatic Aldehydes

inferred← citeshttps://doi.org/10.1002/ejoc.201700470openalex-snapshot

AgI‐Promoted Difluoromethylation of Isocyanides To Give Difluoromethylated Phenanthridines

inferred← citeshttps://doi.org/10.1002/ejoc.201701487openalex-snapshot

Synthesis of 6‐Trifluoromethylphenanthridines through Radical Trifluoromethylation of Isocyanides with Sodium Triflinate under Visible Light

inferred← citeshttps://doi.org/10.1002/ejoc.201901278openalex-snapshot

6‐Arylphenanthridines from Aryl o‐Biaryl Ketones with 1,1,1,3,3,3‐Hexamethyldisilazane and Molecular Iodine

inferred← citeshttps://doi.org/10.1002/ejoc.202001059openalex-snapshot

Metal‐Free Electrochemical Coupling of Vinyl Azides: Synthesis of Phenanthridines and β‐Ketosulfones

inferred← citeshttps://doi.org/10.1002/ejoc.202201269openalex-snapshot

Tandem Sulfonylation/Cyclization of Vinyl Azides with Aryldiazonium Tetrafluoroborates and SO2

inferred← citeshttps://doi.org/10.1002/fsn3.71958openalex-snapshot

Analysis of Quality Differences in Rhizoma Musae From Different Origins Based on Rhizosphere Soil Bacterial Diversity and Metabolomics

inferred← citeshttps://doi.org/10.1002/slct.202500082openalex-snapshot

Mesoporous Graphitic Carbon Nitride Photocatalyzed 6‑Substituted Phenanthridines Synthesis from 2‑Isocyanobiaryls

inferred← citeshttps://doi.org/10.1002/tcr.202100218openalex-snapshot

Synthesis of Six‐Membered N‐Heterocycle Frameworks Based on Intramolecular Metal‐Free N‐Centered Radical Chemistry

inferred← citeshttps://doi.org/10.1007/7081_2017_9openalex-snapshot

Synthesis of Nitrogen-Containing Heterocycles via Imidoyl or Iminyl Radical Intermediates

inferred← citeshttps://doi.org/10.1007/978-3-642-22144-6_18openalex-snapshot

Amaryllidaceae Alkaloids

inferred← citeshttps://doi.org/10.1007/978-3-642-36202-6_18-1openalex-snapshot

Amaryllidaceae Alkaloids

inferred← citeshttps://doi.org/10.1007/978-81-322-2163-0_4openalex-snapshot

Natural Sources of Anti-inflammation

inferred← citeshttps://doi.org/10.1007/978-981-15-8127-4_4openalex-snapshot

Amaryllidaceae Alkaloids as Anti-inflammatory Agents Targeting Cholinergic Anti-inflammatory Pathway: Mechanisms and Prospects

inferred← citeshttps://doi.org/10.1007/s10593-018-2261-7openalex-snapshot

Transition metal-promoted reactions of diarylphosphine oxides as a synthetic method for organophosphorus heterocyclic compounds

inferred← citeshttps://doi.org/10.1007/s11030-023-10743-2openalex-snapshot

Metal-free 2-isocyanobiaryl-based cyclization reactions: phenanthridine framework synthesis

inferred← citeshttps://doi.org/10.1007/s11418-019-01304-9openalex-snapshot

Two new alkaloids from Crinum asiaticum var. japonicum

inferred← citeshttps://doi.org/10.1007/s11426-014-5118-7openalex-snapshot

Tandem dual C(sp3)-H/C(sp2)-H functionalization: a radical cyclization of 2-isocyanobiphenyl with ether to 6-alkylated phenanthridine

inferred← citeshttps://doi.org/10.1016/b978-0-444-63601-0.00003-xopenalex-snapshot

Cytotoxic Alkaloid Constituents of the Amaryllidaceae

inferred← citeshttps://doi.org/10.1016/bs.alkal.2019.10.002openalex-snapshot

Chemodiversity, chemotaxonomy and chemoecology of Amaryllidaceae alkaloids

inferred← citeshttps://doi.org/10.1016/j.bmc.2004.03.020openalex-snapshot

Absolute stereostructures of polypodane- and octanordammarane-type triterpenes with nitric oxide production inhibitory activity from guggul-gum resins

inferred← citeshttps://doi.org/10.1016/j.bmc.2005.02.022openalex-snapshot

1′S-1′-Acetoxychavicol acetate as a new type inhibitor of interferon-β production in lipopolysaccharide-activated mouse peritoneal macrophages

inferred← citeshttps://doi.org/10.1016/j.bmc.2005.08.003openalex-snapshot

Inhibitors from the rhizomes of Alpinia officinarum on production of nitric oxide in lipopolysaccharide-activated macrophages and the structural requirements of diarylheptanoids for the activity

inferred← citeshttps://doi.org/10.1016/j.bmc.2010.01.046openalex-snapshot

Melanogenesis inhibitors from the desert plant Anastatica hierochuntica in B16 melanoma cells

inferred← citeshttps://doi.org/10.1016/j.bmcl.2005.01.070openalex-snapshot

Structure–activity relationships of 1′S-1′-acetoxychavicol acetate for inhibitory effect on NO production in lipopolysaccharide-activated mouse peritoneal macrophages

inferred← citeshttps://doi.org/10.1016/j.fct.2020.111703openalex-snapshot

Acetylcholinesterase inhibitory activity, anti-inflammatory, and neuroprotective potential of Hippeastrum psittacinum (Ker Gawl.) herb (Amaryllidaceae)

inferred← citeshttps://doi.org/10.1016/j.gresc.2021.05.004openalex-snapshot

Planar chiral 2-(trifluoromethyl)quinoline-fused ferrocenes via palladium(0)-catalyzed C-H functionalization of trifluoroacetimidoyl chlorides

inferred← citeshttps://doi.org/10.1016/j.gresc.2026.03.008openalex-snapshot

Visible-light-catalyzed cascade carboxylation/cyclization of o-cyano(bi)arylacrylamides with formate for the synthesis of carboxylated quinolinones and ester-containing phenanthridines

inferred← citeshttps://doi.org/10.1016/j.intimp.2011.11.018openalex-snapshot

Lycorine inhibits lipopolysaccharide-induced iNOS and COX-2 up-regulation in RAW264.7 cells through suppressing P38 and STATs activation and increases the survival rate of mice after LPS challenge

inferred← citeshttps://doi.org/10.1016/j.jep.2024.117943openalex-snapshot

Anti-inflammatory effects of the plant family Amaryllidaceae

inferred← citeshttps://doi.org/10.1016/j.jfluchem.2015.07.028openalex-snapshot

Visible-light-mediated radical difluoromethylenephosphonation of 2-isocyanobiaryls with bromodifluoromethylphosphonate for the synthesis of 6-difluoromethylenephosphonyl-phenanthridines

inferred← citeshttps://doi.org/10.1016/j.jfluchem.2026.110570openalex-snapshot

Visible light-induced photolysis of phosphonium iodides for the radical arylthiodifluoromethylation of isocyanides

inferred← citeshttps://doi.org/10.1016/j.mencom.2020.01.004openalex-snapshot

Cyanoacetylene-driven base catalyzed synthesis of dihydropyrimidophenanthridinones from phenanthridine and water

inferred← citeshttps://doi.org/10.1016/j.mencom.2022.07.004openalex-snapshot

A straightforward access to 2-hydroxyoxazino[3,2-f ]phenanthridines from phenanthridine, oxalylacetylenes and water

inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113929openalex-snapshot

Amaryllidaceae alkaloids from the bulbs of Crinum latifolium L. and their cholinesterase inhibitory activities

inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114383openalex-snapshot

Amaryllidaceae alkaloids with nitric oxide inhibitory activity from the leaves of Crinum asiaticum L. var. asiaticum

inferred← citeshttps://doi.org/10.1016/j.tet.2006.03.091openalex-snapshot

Pseudoguaiane-type sesquiterpenes and inhibitors on nitric oxide production from Dichrocephala integrifolia

inferred← citeshttps://doi.org/10.1016/j.tet.2006.07.027openalex-snapshot

A general approach to crinine-type Amaryllidaceae alkaloids: total syntheses of (±)-haemanthidine, (±)-pretazettine, (±)-tazettine, and (±)-crinamine

inferred← citeshttps://doi.org/10.1016/j.tet.2007.05.041openalex-snapshot

Total synthesis of Amaryllidaceae alkaloids, (+)-vittatine and (+)-haemanthamine, starting from d-glucose

inferred← citeshttps://doi.org/10.1016/j.tet.2010.03.096openalex-snapshot

‘Aromatic ring umpolung’, a rapid access to the main core of several natural products

inferred← citeshttps://doi.org/10.1016/j.tet.2014.05.039openalex-snapshot

Synthesis of phenanthridin-6-yldiphenylphosphine oxides by oxidative cyclization of 2-isocyanobiphenyls with diarylphosphine oxides

inferred← citeshttps://doi.org/10.1016/j.tet.2015.05.064openalex-snapshot

Synthesis and characterization of oxadisilole-fused phenanthridines and dioxatrisilole-fused phenanthridines from benzyne

inferred← citeshttps://doi.org/10.1016/j.tet.2016.11.010openalex-snapshot

Synthesis of 6-aroyl phenanthridines by Fe-catalyzed oxidative radical cyclization of 2-isocyanobiphenyls with benzylic alcohols

inferred← citeshttps://doi.org/10.1016/j.tet.2017.10.074openalex-snapshot

Metal-free photocatalyzed cross coupling of aryl (heteroaryl) bromides with isonitriles

inferred← citeshttps://doi.org/10.1016/j.tet.2019.05.011openalex-snapshot

Palladium catalyzed annulation of benzylamines and arynes via C–H activation to construct 5,6-dihydrophenanthridine derivatives

inferred← citeshttps://doi.org/10.1016/j.tet.2020.131503openalex-snapshot

Preparation of phenanthridines from N-(o-arylbenzyl)trifluoromethanesulfonamides with 1,3-diiodo-5,5-dimethylhydantoin

inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.07.037openalex-snapshot

Synthesis of 5,6-dihydrophenanthridines via N,O-acetal TMS ethers

inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.07.049openalex-snapshot

Synthesis of 6-carboxylated phenanthridines by oxidative alkoxycarbonylation–cyclization of 2-isocyanobiphenyls with carbazates

inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.04.067openalex-snapshot

Metal-free oxidative cascade cyclization of isocyanides with thiols: a new pathway for constructing 6-aryl(alkyl)thiophenanthridines

inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.07.024openalex-snapshot

Direct synthesis of 6-sulfonylated phenanthridines via silver-catalyzed radical sulfonylation-cyclization of 2-isocyanobiphenyls

inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.152908openalex-snapshot

Synthesis of imidazo[1,2-f]phenanthridine derivatives under a metal- and base-free condition and their anticancer activity

inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155557openalex-snapshot

Synthesis of Phenanthridine derivatives from Arynes and Ketimines via aza-Diels-Alder/decarboxylation reactions

inferred← citeshttps://doi.org/10.1016/s1099-4831(06)63003-4openalex-snapshot

Chapter 3 Chemical and Biological Aspects of Narcissus Alkaloids

inferred← citeshttps://doi.org/10.1021/acs.joc.0c00816openalex-snapshot

Visible-Light-Driven Difluoromethylation of Isocyanides with S -(Difluoromethyl)diarylsulfonium Salt: Access to a Wide Variety of Difluoromethylated Phenanthridines and Isoquinolines

inferred← citeshttps://doi.org/10.1021/acs.joc.0c01390openalex-snapshot

Synthesis of Phenanthridines through Iodine-Supported Intramolecular C–H Amination and Oxidation under Visible Light

inferred← citeshttps://doi.org/10.1021/acs.joc.3c00056openalex-snapshot

Difluoromethylborates and Muonium for the Study of Isonitrile Insertion Affording Phenanthridines via Imidoyl Radicals

inferred← citeshttps://doi.org/10.1021/acs.joc.5b01518openalex-snapshot

Transition Metal-Free Oxidative Radical Decarboxylation/Cyclization for the Construction of 6-Alkyl/Aryl Phenanthridines

inferred← citeshttps://doi.org/10.1021/acs.joc.5b02903openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/acs.joc.5c01891openalex-snapshot

Visible-Light-Induced Cascade Cyclization of Isocyanobiaryls with Hydrosilanes for the Synthesis of 6-Silylated Phenanthridines

inferred← citeshttps://doi.org/10.1021/acs.joc.5c02890openalex-snapshot

Photocatalytic Silylation/Germylation and Cascade Cyclization of N -( o -Cyanobiaryl)acrylamides: Access to Silylated and Germylated Phenanthridines

inferred← citeshttps://doi.org/10.1021/acs.joc.6b00885openalex-snapshot

Synthesis of 6-Trichloromethylphenanthridines by Transition Metal-Free Radical Cyclization of 2-Isocyanobiphenyls

inferred← citeshttps://doi.org/10.1021/acs.joc.6c00246openalex-snapshot

Photochemical, Pd-Catalyzed Activation of Alkyl Bromides and Chlorides for Alkylative Cascade Cyclization of O -Cyano Acrylamides

inferred← citeshttps://doi.org/10.1021/acs.joc.7b00343openalex-snapshot

Synthesis of Cyano-Containing Phenanthridine Derivatives via Catalyst-, Base-, and Oxidant-Free Direct Cyanoalkylarylation of Isocyanides

inferred← citeshttps://doi.org/10.1021/acs.joc.8b00924openalex-snapshot

Metal-Catalyzed Domino Synthesis of Benzophenanthridines and 6H-Naphtho[2,3-c]-chromenes

inferred← citeshttps://doi.org/10.1021/acs.joc.8b01688openalex-snapshot

Preparation of Phenanthridines from o-Cyanobiaryls via Addition of Organic Lithiums to Nitriles and Imino Radical Cyclization with Iodine

inferred← citeshttps://doi.org/10.1021/acs.joc.9b00018openalex-snapshot

Application of Electrocyclic Ring-Opening and Desymmetrizing Nucleophilic Trappings of meso-6,6-Dibromobicyclo[3.1.0]hexanes to Total Syntheses of Crinine and Haemanthamine Alkaloids

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03013openalex-snapshot

Radical (Phenylsulfonyl)difluoromethylation of Isocyanides with PhSO2CF2H under Transition-Metal-Free Conditions

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01771openalex-snapshot

Silver-Catalyzed Tandem C≡C Bond Hydroazidation/Radical Addition/Cyclization of Biphenyl Acetylene: One-Pot Synthesis of 6-Methyl Sulfonylated Phenanthridines

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00171openalex-snapshot

Photo-Driven Synthesis of C6-Polyfunctionalized Phenanthridines from Three-Component Reactions of Isocyanides, Alkynes, and Sulfinic Acids by Electron Donor–Acceptor Complex

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01510openalex-snapshot

Synthesis of Chloro(phenyl)trifluoromethyliodane and Catalyst-Free Electrophilic Trifluoromethylations

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02588openalex-snapshot

Expeditious Synthesis of 6-Fluoroalkyl-Phenanthridines via Palladium-Catalyzed Norbornene-Mediated Dehydrogenative Annulation

inferred← citeshttps://doi.org/10.1021/acscatal.9b04274openalex-snapshot

Ir-Catalyzed Cascade C–H Fusion of Aldoxime Ethers and Heteroarenes: Scope and Mechanisms

inferred← citeshttps://doi.org/10.1021/jo3027033openalex-snapshot

Synthesis of Phenanthridine Derivatives by Microwave-Mediated Cyclization of o -Furyl(allylamino)arenes

inferred← citeshttps://doi.org/10.1021/jo500842eopenalex-snapshot

Radical Arylalkoxycarbonylation of 2-Isocyanobiphenyl with Carbazates: Dual C–C Bond Formation toward Phenanthridine-6-carboxylates

inferred← citeshttps://doi.org/10.1021/jo501910qopenalex-snapshot

Palladium-Catalyzed Regiocontrolled Domino Synthesis of N-Sulfonyl Dihydrophenanthridines and Dihydrodibenzo[c,e]azepines: Control over the Formation of Biaryl Sultams in the Intramolecular Direct Arylation

inferred← citeshttps://doi.org/10.1021/jo801761fopenalex-snapshot

Suzuki Cross-Coupling/Reductive Debenzyloxycarbonylation Sequence for the Syntheses of [c]Annulated Isoquinolines: Application for the Syntheses of Pancratistatin-like Isoquinolines

inferred← citeshttps://doi.org/10.1021/jo9025918openalex-snapshot

Electron-Transfer-Mediated Synthesis of Phenanthridines by Intramolecular Arylation of Anions from N-(ortho-Halobenzyl)arylamines: Regiochemical and Mechanistic Analysis

inferred← citeshttps://doi.org/10.1021/np0702077openalex-snapshot

Benzylphenethylamine Alkaloids from Hosta plantaginea with Inhibitory Activity against Tobacco Mosaic Virus and Acetylcholinesterase

inferred← citeshttps://doi.org/10.1021/np3005425openalex-snapshot

Cytotoxic Alkaloids from the Whole Plants of Zephyranthes candida

inferred← citeshttps://doi.org/10.1021/ol403147vopenalex-snapshot

6-Aroylated Phenanthridines via Base Promoted Homolytic Aromatic Substitution (BHAS)

inferred← citeshttps://doi.org/10.1021/ol403256eopenalex-snapshot

6-Phosphorylated Phenanthridines from 2-Isocyanobiphenyls via Radical C–P and C–C Bond Formation

inferred← citeshttps://doi.org/10.1021/ol500277uopenalex-snapshot

The Benzoyl Peroxide Promoted Dual C–C Bond Formation via Dual C–H Bond Cleavage: α-Phenanthridinylation of Ether by Isocyanide

inferred← citeshttps://doi.org/10.1021/ol500286xopenalex-snapshot

Co(acac)2/O2-Mediated Oxidative Isocyanide Insertion with 2-Aryl Anilines: Efficient Synthesis of 6-Amino Phenanthridine Derivatives

inferred← citeshttps://doi.org/10.1021/ol500314xopenalex-snapshot

One-Pot Cascade Approach to Phenanthridine-Fused Quinazoliniminiums from Heteroenyne-Allenes

inferred← citeshttps://doi.org/10.1021/ol503335kopenalex-snapshot

Synthesis of Isoxazoline-Functionalized Phenanthridines via Iminoxyl Radical-Participated Cascade Sequence

inferred← citeshttps://doi.org/10.1021/ol902000jopenalex-snapshot

An Unprecedented Oxidative Wagner−Meerwein Transposition

inferred← citeshttps://doi.org/10.1038/s41467-023-40891-wopenalex-snapshot

Catalytic asymmetric dearomatization of phenols via divergent intermolecular (3 + 2) and alkylation reactions

inferred← citeshttps://doi.org/10.1039/b502163bopenalex-snapshot

Amaryllidaceae and Sceletium alkaloids

inferred← citeshttps://doi.org/10.1039/b716519fopenalex-snapshot

Phenanthridine synthesis via [2+2+2] cyclotrimerization reactions

inferred← citeshttps://doi.org/10.1039/c3np70005dopenalex-snapshot

Amaryllidaceae and Sceletium alkaloids

inferred← citeshttps://doi.org/10.1039/c4cc00743copenalex-snapshot

tert-Butyl peroxybenzoate (TBPB)-mediated 2-isocyanobiaryl insertion with 1,4-dioxane: efficient synthesis of 6-alkyl phenanthridines via C(sp3)–H/C(sp2)–H bond functionalization

inferred← citeshttps://doi.org/10.1039/c4cc01487aopenalex-snapshot

Transition-metal-free, visible-light induced cyclization of arylsulfonyl chlorides with 2-isocyanobiphenyls to produce phenanthridines

inferred← citeshttps://doi.org/10.1039/c4cc03304copenalex-snapshot

The benzoyl peroxide-promoted functionalization of simple alkanes with 2-aryl phenyl isonitrile

inferred← citeshttps://doi.org/10.1039/c4cc04773gopenalex-snapshot

TBHP-promoted sequential radical silylation and aromatisation of aryl isonitriles with silanes

inferred← citeshttps://doi.org/10.1039/c4ob01256aopenalex-snapshot

A cascade alkylarylation reaction of 2-isocyanobiphenyls with simple alkanes for 6-alkyl phenanthridines via dual C(sp 3 )–H/C(sp 2 )–H functionalizations

inferred← citeshttps://doi.org/10.1039/c4ob01850hopenalex-snapshot

TBHP-promoted sequential carboxamidation and aromatisation of aryl isonitriles with formamides

inferred← citeshttps://doi.org/10.1039/c4ra02381aopenalex-snapshot

Synthesis of 6-aminophenanthridines via palladium-catalyzed insertion of isocyanides into N-sulfonyl-2-aminobiaryls

inferred← citeshttps://doi.org/10.1039/c4ra06159dopenalex-snapshot

PhI(OAc) 2 –BF 3 –OEt 2 mediated domino imine activation, intramolecular C–C bond formation and β-elimination: new approach for the synthesis of fluorenones, xanthones and phenanthridines

inferred← citeshttps://doi.org/10.1039/c5cc08872kopenalex-snapshot

Radical C–H functionalization to construct heterocyclic compounds

inferred← citeshttps://doi.org/10.1039/c5cc09179aopenalex-snapshot

Silver-catalyzed oxidative decarboxylation of difluoroacetates: efficient access to C–CF 2 bond formation

inferred← citeshttps://doi.org/10.1039/c5cs00083aopenalex-snapshot

Recent advances in the synthesis of nitrogen heterocycles via radical cascade reactions using isonitriles as radical acceptors

inferred← citeshttps://doi.org/10.1039/c5ra16645dopenalex-snapshot

Light triggered addition/annulation of 2-isocyanobiphenyls toward 6-trifluoromethyl-phenanthridines under photocatalyst-free conditions

inferred← citeshttps://doi.org/10.1039/c6ob00087hopenalex-snapshot

Recent progress in imidoyl radical-involved reactions

inferred← citeshttps://doi.org/10.1039/c6ob02103dopenalex-snapshot

A radical addition/cyclization of diverse ethers to 2-isocyanobiaryls under mildly basic aqueous conditions

inferred← citeshttps://doi.org/10.1039/c7cc01813dopenalex-snapshot

Visible-light-mediated radical insertion/cyclization cascade reaction: synthesis of phenanthridines and isoquinolines from isocyanides

inferred← citeshttps://doi.org/10.1039/c7cc05411dopenalex-snapshot

Silver-mediated oxidative C–H difluoromethylation of phenanthridines and 1,10-phenanthrolines

inferred← citeshttps://doi.org/10.1039/c7qo00473gopenalex-snapshot

Transition-metal-free radical fluoroalkylation of isocyanides for the synthesis of tri-/di-/monofluoromethylated phenanthridines

inferred← citeshttps://doi.org/10.1039/c7qo00790fopenalex-snapshot

Visible-light-induced sulfonylation/cyclization of vinyl azides: one-pot construction of 6-(sulfonylmethyl)phenanthridines

inferred← citeshttps://doi.org/10.1039/c7ra12318copenalex-snapshot

Use of unprotected amino acids in metal-free tandem radical cyclization reactions: divergent synthesis of 6-alkyl/acyl phenanthridines

inferred← citeshttps://doi.org/10.1039/c8cc03556copenalex-snapshot

Rapid synthesis of polysubstituted phenanthridines from simple aliphatic/aromatic nitriles and iodo arenes via Pd( ii ) catalyzed domino C–C/C–C/C–N bond formation

inferred← citeshttps://doi.org/10.1039/c8ob02462fopenalex-snapshot

Iron-catalyzed cascade addition/cyclization of 2-biphenyl isocyanides with toluenes: a highly efficient approach to 6-benzylated phenanthridines

inferred← citeshttps://doi.org/10.1039/c8ob02786bopenalex-snapshot

Radical alkylation of isocyanides with amino acid-/peptide-derived Katritzky salts via photoredox catalysis

inferred← citeshttps://doi.org/10.1039/c8qo00679bopenalex-snapshot

Synthesis of 6-(sulfonylmethyl)phenanthridines through a reaction of aryldiazonium tetrafluoroborates, sulfur dioxide, and vinyl azides

inferred← citeshttps://doi.org/10.1039/d0ob00136hopenalex-snapshot

Photocatalytic xanthate-based radical addition/cyclization reaction sequence toward 2-biphenyl isocyanides: synthesis of 6-alkylated phenanthridines

inferred← citeshttps://doi.org/10.1039/d0ra03211eopenalex-snapshot

PPh 3 /NaI driven photocatalytic decarboxylative radical cascade alkylarylation reaction of 2-isocyanobiaryls

inferred← citeshttps://doi.org/10.1039/d1gc02670dopenalex-snapshot

Selective C(sp 3 )–H activation of simple alkanes: visible light-induced metal-free synthesis of phenanthridines with H 2 O 2 as a sustainable oxidant

inferred← citeshttps://doi.org/10.1039/d2nj00579dopenalex-snapshot

Synthesis of indenophenanthridine via a [4+2] annulation strategy: a “turn-off’’ Fe 3+ ion sensor, practical application in live cell imaging and reversible acidochromism studies

inferred← citeshttps://doi.org/10.1039/d3ob00239jopenalex-snapshot

Electrochemical trifluoromethylation of 2-isocyanobiaryls using CF 3 SO 2 Na: synthesis of 6-(trifluoromethyl)phenanthridines

inferred← citeshttps://doi.org/10.1039/d3ob00588gopenalex-snapshot

Visible light-assisted chemistry of vinyl azides and its applications in organic synthesis

inferred← citeshttps://doi.org/10.1039/d3qo00780dopenalex-snapshot

Synthesis of ester-containing phenanthridines via photoredox-catalyzed radical cascade cyclization of N -arylacrylamides with alkyloxalyl chlorides

inferred← citeshttps://doi.org/10.1039/d4ob02085eopenalex-snapshot

Bromide-promoted cascade annulation of isocyanobiaryls with aldehydes through photoredox catalysis

inferred← citeshttps://doi.org/10.1039/d5ob00530bopenalex-snapshot

Photoinduced N-heterocyclic nitrenium-catalyzed single electron reduction of α-chloro esters for phenanthridine synthesis

inferred← citeshttps://doi.org/10.1039/d5qo01301aopenalex-snapshot

A unified strategy to access N-heterocycles enabled by hypervalent iodine( iii ) reagent-mediated imidate radical cyclization

inferred← citeshttps://doi.org/10.1055/a-1380-1888openalex-snapshot

Cytotoxic Agents in the Minor Alkaloid Groups of the Amaryllidaceae

inferred← citeshttps://doi.org/10.1055/a-1782-7150openalex-snapshot

Potassium tert-Butoxide Promoted Intramolecular Mizoroki–Heck-Type Radical Cyclization: Photoluminescence Properties and Application in Live Cancer-Cell Imaging

inferred← citeshttps://doi.org/10.1055/a-2369-8104openalex-snapshot

Anti-inflammatory Principles of the Plant Family Amaryllidaceae

inferred← citeshttps://doi.org/10.1055/a-2788-6538openalex-snapshot

Synthesis of (+)-Dehydrobulbispermine Analogs

inferred← citeshttps://doi.org/10.1055/s-0036-1588929openalex-snapshot

Radical Cyclopropanol Ring Opening Initiated Tandem Cyclizations for Efficient Synthesis of Phenanthridines and Oxindoles

inferred← citeshttps://doi.org/10.1070/rcr4525openalex-snapshot

Phosphorylation of C–H bonds of aromatic compounds using metals and metal complexes

inferred← citeshttps://doi.org/10.1074/jbc.m116.717827openalex-snapshot

Identification of a Noroxomaritidine Reductase with Amaryllidaceae Alkaloid Biosynthesis Related Activities

inferred← citeshttps://doi.org/10.1080/07391102.2023.2238065openalex-snapshot

Investigation of bio-active Amaryllidaceae alkaloidal small molecules as putative SARS-CoV-2 main protease and host TMPRSS2 inhibitors: interpretation by in-silico simulation study

inferred← citeshttps://doi.org/10.1080/10286020.2016.1198332openalex-snapshot

Phytochemical and biological investigations of Amaryllidaceae alkaloids: a review

inferred← citeshttps://doi.org/10.1080/14786419.2026.2690079openalex-snapshot

An undescribed alkaloid from Crinum latifolium L.: structural elucidation and evaluation of its biological activity

inferred← citeshttps://doi.org/10.1155/2020/2529730openalex-snapshot

Antiproliferative Effects of Alkaloids from the Bulbs of Crinum abyscinicum Hochst. ExA. Rich

inferred← citeshttps://doi.org/10.1177/1934578x1400900834openalex-snapshot

Cytotoxicity Studies of Lycorine Alkaloids of the Amaryllidaceae

inferred← citeshttps://doi.org/10.1177/1934578x1501000138openalex-snapshot

Mechanistic Insights to the Cytotoxicity of Amaryllidaceae Alkaloids

inferred← citeshttps://doi.org/10.1201/b13867-16openalex-snapshot

Plant Metabolites: Inhibitors of NO Production

inferred← citeshttps://doi.org/10.1246/cl.180009openalex-snapshot

Silver(I)-mediated Reaction of 2-Isocyanobiaryl with Alkyl Trifluoroborates: Efficient Synthesis of 6-Alkylated Phenanthridines

inferred← citeshttps://doi.org/10.1248/bpb.29.2140openalex-snapshot

Crinamine from Crinum asiaticum var. japonicum Inhibits Hypoxia Inducible Factor-1 Activity But Not Activity of Hypoxia Inducible Factor-2

inferred← citeshttps://doi.org/10.1248/bpb.32.147openalex-snapshot

Bioactive Constituents from Chinese Natural Medicines. XXXIII. Inhibitors from the Seeds of Psoralea corylifolia on Production of Nitric Oxide in Lipopolysaccharide-Activated Macrophages

inferred← citeshttps://doi.org/10.1248/cpb.53.387openalex-snapshot

Inhibitors of Nitric Oxide Production from the Flowers of Angelica furcijuga: Structures of Hyuganosides IV and V

inferred← citeshttps://doi.org/10.1248/cpb.53.625openalex-snapshot

Inhibitors of Nitric Oxide Production from the Rhizomes of Alpinia galanga: Structures of New 8-9' Linked Neolignans and Sesquineolignan

inferred← citeshttps://doi.org/10.1248/cpb.54.1530openalex-snapshot

Structures of New Flavonoids, Erycibenins D, E, and F, and NO Production Inhibitors from Erycibe expansa Originating in Thailand

inferred← citeshttps://doi.org/10.1248/cpb.55.428openalex-snapshot

Bioactive Saponins and Glycosides. XXVII. Structures of New Cucurbitane-Type Triterpene Glycosides and Antiallergic Constituents from Citrullus colocynthis

inferred← citeshttps://doi.org/10.1248/cpb.57.957openalex-snapshot

Absolute Stereostructures of Olibanumols A, B, C, H, I, and J from Olibanum, Gum-Resin of Boswellia carterii, and Inhibitors of Nitric Oxide Production in Lipopolysaccharide-Activated Mouse Peritoneal Macrophages

inferred← citeshttps://doi.org/10.1248/cpb.58.1379openalex-snapshot

Structures of Novel Norstilbene Dimer, Longusone A, and Three New Stilbene Dimers, Longusols A, B, and C, with Antiallergic and Radical Scavenging Activities from Egyptian Natural Medicine Cyperus longus

inferred← citeshttps://doi.org/10.1248/cpb.58.1541openalex-snapshot

Four New Ursane-Type Triterpenes, Olibanumols K, L, M, and N, from Traditional Egyptian Medicine Olibanum, the Gum-Resin of Boswellia carterii

inferred← citeshttps://doi.org/10.1248/cpb.58.747openalex-snapshot

Cucurbitane-Type Triterpenes with Anti-proliferative Effects on U937 Cells from an Egyptian Natural Medicine, Bryonia cretica: Structures of New Triterpene Glycosides, Bryoniaosides A and B

inferred← citeshttps://doi.org/10.2174/0115701786430407251203102234openalex-snapshot

Recent Advances in Catalytic Synthetic Routes for Quinazolino [3, 2-f] Phenanthridin-14-one Derivatives Derived From 2-Arylquinazolinones: A Review

inferred← citeshttps://doi.org/10.3390/biom9090494openalex-snapshot

Crinamine Induces Apoptosis and Inhibits Proliferation, Migration, and Angiogenesis in Cervical Cancer SiHa Cells

inferred← citeshttps://doi.org/10.3390/catal12111446openalex-snapshot

Photoredox-Catalyzed Acylation/Cyclization of 2-Isocyanobiaryls with Oxime Esters for the Synthesis of 6-Acyl Phenanthridines

inferred← citeshttps://doi.org/10.3390/ijms21165868openalex-snapshot

Oxidative Photocyclization of Aromatic Schiff Bases in Synthesis of Phenanthridines and Other Aza-PAHs

inferred← citeshttps://doi.org/10.3390/molecules21050660openalex-snapshot

Synthetic Strategies for 5- and 6-Membered Ring Azaheterocycles Facilitated by Iminyl Radicals

inferred← citeshttps://doi.org/10.3390/molecules27144475openalex-snapshot

The Phytochemistry and Pharmacology of Tulbaghia, Allium, Crinum and Cyrtanthus: ‘Talented’ Taxa from the Amaryllidaceae

inferred← citeshttps://doi.org/10.3390/molecules28062498openalex-snapshot

Synthesis of 5,6-Dihydrophenanthridines via Palladium-Catalyzed Intramolecular Dehydrogenative Coupling of Two Aryl C−H Bonds

inferred← citeshttps://doi.org/10.3390/plants15081186openalex-snapshot

Alkaloids from In Vitro Cultured Rhodophiala pratensis Display Neuroprotective Effects in Murine Microglial Cell Models of Inflammation

inferred← citeshttps://doi.org/10.3987/com-17-13754openalex-snapshot

Synthesis of Highly Substituted 5,6-Dihydrobenzo[j]phenanthridine Derivatives via Domino Reaction

inferred← citeshttps://doi.org/10.48130/mpb-0025-0038openalex-snapshot

Biosynthesis, total synthesis, and pharmacological activities of galanthamine and its analogues

inferred← citeshttps://doi.org/10.5487/tr.2008.24.1.029openalex-snapshot

The Effects of Crinum asiaticum on the Apoptosis Induction and the Reversal of Multidrug Resistance in HL-60/MX2

inferred← citeshttps://doi.org/10.6023/cjoc202102025openalex-snapshot

t-BuOK-Mediated Reductive Desulfonylation/Dehydrogenation for the Synthesis of 2-Substituted 1,3-Dienes and Their [4+2] Cycloaddition Reactions

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