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Indole Alkaloids from Cephalanceropsis gracilis

https://doi.org/10.1021/np060395l
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inferredcites →https://doi.org/10.1002/cber.19821150111openalex-snapshot
Reaktionen mit Nitrosodisulfonat, 40. Oxidation von Keto‐Enolen
inferredcites →https://doi.org/10.1021/jm030561bopenalex-snapshot
Generation of New Protein Kinase Inhibitors Utilizing Cytochrome P450 Mutant Enzymes for Indigoid Synthesis
inferredcites →https://doi.org/10.1021/jo050257lopenalex-snapshot
Dipeptide-Catalyzed Asymmetric Aldol Condensation of Acetone with (N-Alkylated) Isatins
inferredcites →https://doi.org/10.1039/b516152eopenalex-snapshot
Expedient synthesis and structure–activity relationships of phenanthroindolizidine and phenanthroquinolizidine alkaloids

What points at this work

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

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B(C6f5)3-Catalyzed Regio- and Stereoselective Cyanation of Isatogens and Their Derivatives
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Green Catalysis for Chemical Transformation
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N‐Heterocyclic Carbene‐Catalyzed Umpolung Formal [3+3] Cycloaddition of Enals with Isatogens: Access to Fused Indolin‐3‐ones with a Tetrasubstituted Carbon Stereocenter
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Palladium‐Catalyzed Domino Synthesis of 2,3‐Difunctionalized Indoles via Migratory Insertion of Isocyanides in Batch and Continuous Flow
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Cobalt‐Catalyzed Cascade Reaction of Ynamides and 1,3‐Dicarbonyl Compounds for Selective Synthesis of Differently Sized N‐Heterocycles
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Copper‐Catalyzed Oxidative Intramolecular Cyclization for the Synthesis of 2‐Hydroxy‐Indolin‐3‐Ones
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Ru(II)‐Catalyzed C3‐H Functionalization of Indoles With Isatogens
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Stereoselective Organocatalytic Synthesis of Oxindoles with Adjacent Tetrasubstituted Stereocenters
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Expanding the Promiscuity of a Copper‐Dependent Oxidase for Enantioselective Cross‐Coupling of Indoles
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Stereoselective Organocatalytic Synthesis of Oxindoles with Adjacent Tetrasubstituted Stereocenters
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Expanding the Promiscuity of a Copper‐Dependent Oxidase for Enantioselective Cross‐Coupling of Indoles
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Oxidative Asymmetric Aza‐Friedel–Crafts Alkylation of Indoles with 3‐Indolinone‐2‐carboxylates Catalyzed by a BINOL Phosphoric Acid and Promoted by DDQ
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InCl3‐Mediated Addition of Indole to Isatogens: An Expeditious Synthesis of 13‐deoxy‐Isatisine A
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Photoinduced Ring‐Opening and Phototoxicity of an Indolin‐3‐one Derivative
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Microwave Promoted Tandem Reaction of Free Primary Arylamines with Diazo Compounds Under Metal‐Free Condition in Water: Clean Synthesis of 2,2‐Disubstituted 3‐Oxindoles
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Oxidative Coupling of 3‐Oxindoles with Indoles and Arenes
inferred← citeshttps://doi.org/10.1002/ejoc.201701670openalex-snapshot
Organocatalytic Enantioselective Michael Addition of 3‐Indolinone‐2‐Carboxylates to Maleimides
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Elucidating ‘undecipherable’ chemical structures using computer‐assisted structure elucidation approaches
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Synthesis of Indole‐2‐methylsulfonamides by Domino Sonogashira Coupling and Hydroamination Reaction
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Pd‐Catalyzed One‐Pot Two‐Step Synthesis of 2‐(1 H ‐indol‐3‐yl)‐2‐phenylindolin‐3‐ones from 2‐Alkynyl Arylazides and Indoles
inferred← citeshttps://doi.org/10.1002/slct.202101238openalex-snapshot
Synthesis of Tetracyclic Indolines through Palladium‐Catalyzed Asymmetric Dearomative reaction of Aryl Iodides
inferred← citeshttps://doi.org/10.1007/s10600-022-03872-xopenalex-snapshot
Indole Alkaloids from the Cigar Tobacco-Derived Endophytic Fungus Aspergillus oryzae and Their Antibacterial Activity
inferred← citeshttps://doi.org/10.1016/b978-0-443-27482-4.00009-5openalex-snapshot
Introduction to sonochemistry: Utilizing ultrasound for the synthesis of natural products and biologically relevant heterocycles of medicinal significance
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Pyrroles and their Benzo Derivatives: Applications
inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.06.015openalex-snapshot
Four new minor brominated indole related alkaloids with antibacterial activities from Laurencia similis
inferred← citeshttps://doi.org/10.1016/j.bse.2020.104163openalex-snapshot
Alkaloids from the leaves of Isatis indigotica fortune and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.bse.2022.104488openalex-snapshot
Phytochemical Investigation on Raphanus Sativus L
inferred← citeshttps://doi.org/10.1016/j.bse.2022.104522openalex-snapshot
Chemical constituents from Dendrobium chrysanthum and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.cclet.2015.05.052openalex-snapshot
Antiviral enantiomers of a bisindole alkaloid with a new carbon skeleton from the roots of Isatis indigotica
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.06.003openalex-snapshot
An efficient synthesis and biological evaluation of novel analogues of natural product Cephalandole A: A new class of antimicrobial and antiplatelet agents
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.120718openalex-snapshot
Targeted discovery of anthranilic acid-based alkaloids with neuroprotective and acetylcholinesterase inhibitory effects from natural indigo plant (Persicaria tinctoria) using DeepSAT technology
inferred← citeshttps://doi.org/10.1016/j.jep.2020.112772openalex-snapshot
IL-17A inhibitions of indole alkaloids from traditional Chinese medicine Qing Dai
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.137445openalex-snapshot
‘Cephalandole A’ analogues as a new class of antioxidant agents: Design, microwave-assisted synthesis, bioevaluation, SAR and in silico studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.144519openalex-snapshot
Wang-OSO3H catalyzed sonochemical synthesis of 3-indolylbenzoxazin-2-one derivatives as potential inhibitors of PDE4B
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.02.016openalex-snapshot
Indole alkaloids indigodoles A–C from aerial parts of Strobilanthes cusia in the traditional Chinese medicine Qing Dai have anti-IL-17 properties
inferred← citeshttps://doi.org/10.1016/j.phytol.2025.103013openalex-snapshot
Structurally diverse alkaloids from stems and leaves of Baphicacanthus cusia and their neuraminidase inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.tet.2013.11.026openalex-snapshot
The synthesis of the central tricyclic core of the isatisine A: harmonious orchestration of [metal]-catalyzed reactions in a sequence
inferred← citeshttps://doi.org/10.1016/j.tet.2016.06.046openalex-snapshot
Base-promoted domino reaction for the synthesis of 2,3-disubstituted indoles from 2-aminobenzaldehyde/2-amino aryl ketones, tosylhydrazine, and aromatic aldehydes
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130620openalex-snapshot
BINOL-phosphoric acid catalyzed asymmetric Mannich addition of β-ketoesters to indolenines generated in situ by DDQ
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.03.048openalex-snapshot
“On water” ultrasound-assisted one pot efficient synthesis of functionalized 2-oxo-benzo[1,4]oxazines: First application to the synthesis of anticancer indole alkaloid, Cephalandole A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.07.002openalex-snapshot
Highly diastereo- and enantioselective construction of phthalide-oxindole hybrids bearing vicinal quaternary chiral centers via an organocatalytic allylic alkylation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154184openalex-snapshot
Silver-catalyzed cross-dehydrogenative coupling of benzoxazine-2-ones with resorcinol
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.154909openalex-snapshot
B(C6F5)3-catalyzed regio- and stereoselective cyanation of isatogens and their derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155626openalex-snapshot
Regio- and Stereoselective [3 + 2] cycloaddition of Isatogens with functionalized alkenes and its application to the synthesis of Halichrome A
inferred← citeshttps://doi.org/10.1016/j.xcrp.2021.100577openalex-snapshot
Controllable synthesis of benzoxazinones and 2-hydroxy-3-indolinones by visible-light-promoted 5-endo-dig N-radical cyclization cascade
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α-Keto Acids: Acylating Agents in Organic Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00949openalex-snapshot
Baphicacanthcusines A–E, Bisindole Alkaloids from the Leaves of Baphicacanthus cusia (Nees) Bremek
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01485openalex-snapshot
Synthesis of Hydroxysuccinimide Substituted Indolin-3-ones via One-Pot Cascade Reaction of o-Alkynylnitrobenzenes with Maleimides under Au(III)–Cu(II) Relay/Synergetic Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02644openalex-snapshot
Anodic C(sp3)–H Acyloxylation of Indolin-3-ones Enabled by Oxidant-Free Cross-Dehydrogenative C(sp3)–O Coupling
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01209openalex-snapshot
Palladium-Catalyzed Intramolecular Heck Dearomative Alkenylation of Indoles with N-Tosylhydrazones
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02599openalex-snapshot
Pd-Catalyzed Asymmetric Allylation Reaction of 2-Aryl-3H-indol-3-ones with Allyltrimethylsilane
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02807openalex-snapshot
Enantioselective Synthesis of C2-Quaternary Indolin-3-ones by Pt-Catalyzed Alkynylation of 2-Aryl-3 H -indol-3-one with Alkynylsilanes
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00873openalex-snapshot
Synthesis of 2,2-Disubstituted Indolin-3-ones via Enolonium Species
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01028openalex-snapshot
High Enantioselective and Unprecedented Diastereoselective Synthesis of C2-Quaternary Indolin-3-ones by CPA-Catalyzed Asymmetric Mannich Reaction of 3,3-Difluoro-2-aryl-3H-indoles with Cycloketones
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02847openalex-snapshot
Direct Synthesis of 2-Alkynylindolin-3-ones via Copper-Catalyzed Reductive Alkynylation of 2-Arylisatogens
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02893openalex-snapshot
Oxidative Recyclization of 1H-Indoles for Synthesis of 2-Indolylbenzoxazinones via Cleavage of the C2–C3 Bond with AIBN under Air
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02423openalex-snapshot
TfOH-Catalyzed Reaction between 3-Diazoindolin-2-imines and Electron-Rich Arenes: Access to 3-Aryl-2-aminoindoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01096openalex-snapshot
A Hg(OTf)2-Catalyzed Enolate Umpolung Reaction Enables the Synthesis of Coumaran-3-ones and Indolin-3-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01811openalex-snapshot
Ruthenium(II)-Catalyzed Ortho-C–H Alkylation of Naphthylamines with Diazo Compounds for Synthesis of 2,2-Disubstituted π-Extended 3-Oxindoles in Water
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02323openalex-snapshot
Selective Synthesis of 2-Indolyl-3-oxoindolines or 2-(2-Aminophenyl)quinolines through Cu(II)- or Bi(III)-Catalyzed Tunable Dimerizations of 2-Alkynylanilines
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03150openalex-snapshot
B(C 6 F 5 ) 3 -Catalyzed Highly Chemoselective Reduction of Isatins: Synthesis of Indolin-3-ones and Indolines
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03011openalex-snapshot
Metal-Free Oxidative Dearomatization–Alkoxylation/Acyloxylation of Indoles: Synthesis of 2-Monosubstituted Indolin-3-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03480openalex-snapshot
KI-Catalyzed C(sp3)–H Amination and Acyloxylation of Indolin-3-ones Using Air as the Oxidant
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01720openalex-snapshot
Heteroannulation of Arynes with α-Bromodifluorohydroxamates: An Efficient and General Approach to Access 2,2-Difluoro Indoxyls
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00244openalex-snapshot
Oxidative Dearomatization of Indoles via Pd-Catalyzed C–H Oxygenation: An Entry to C2-Quaternary Indolin-3-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03473openalex-snapshot
Organocatalytic Enantioselective Amination of 2-Substituted Indolin-3-ones: A Strategy for the Synthesis of Chiral α-Hydrazino Esters
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00200openalex-snapshot
Gold/Copper-Co-catalyzed Tandem Reactions of 2-Alkynylanilines: A Synthetic Strategy for the C2-Quaternary Indolin-3-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03213openalex-snapshot
Catalytic Asymmetric Mukaiyama–Mannich Reaction of Cyclic C-Acylimines with Difluoroenoxysilanes: Access to Difluoroalkylated Indolin-3-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03185openalex-snapshot
Cu-Catalyzed Oxidation of C2 and C3 Alkyl-Substituted Indole via Acyl Nitroso Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00740openalex-snapshot
Annulation Cascades of N -Allyl- N -((2-bromoaryl)ethynyl)amides Involving C–H Functionalization
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01965openalex-snapshot
Organocatalytic Asymmetric Dearomative Oxyalkylation of Indoles Enables Access to C2-Quaternary Indolin-3-ones
inferred← citeshttps://doi.org/10.1021/acscatal.6b01969openalex-snapshot
Visible Light Photocatalytic Aerobic Oxygenation of Indoles and pH as a Chemoselective Switch
inferred← citeshttps://doi.org/10.1021/acsomega.8b02132openalex-snapshot
Organocatalytic Enantioselective Mannich Reaction: Direct Access to Chiral β-Amino Esters
inferred← citeshttps://doi.org/10.1021/ja105035ropenalex-snapshot
Assigning Stereochemistry to Single Diastereoisomers by GIAO NMR Calculation: The DP4 Probability
inferred← citeshttps://doi.org/10.1021/jf301570yopenalex-snapshot
Isolation and Identification of Secondary Metabolites of Clitocybe nuda Responsible for Inhibition of Zoospore Germination of Phytophthora capsici
inferred← citeshttps://doi.org/10.1021/np3002833openalex-snapshot
Alkaloids from the Root of Isatis indigotica
inferred← citeshttps://doi.org/10.1021/np5003274openalex-snapshot
Indole Alkaloid Glycosides from the Aerial Parts of Strobilanthes cusia
inferred← citeshttps://doi.org/10.1021/np800334jopenalex-snapshot
Synthetic Studies of Cephalandole Alkaloids and the Revised Structure of Cephalandole A
inferred← citeshttps://doi.org/10.1038/nchem.765openalex-snapshot
Organic structure determination using atomic-resolution scanning probe microscopy
inferred← citeshttps://doi.org/10.1038/nchem.849openalex-snapshot
Molecules under the microscope
inferred← citeshttps://doi.org/10.1039/9781849734578-00366openalex-snapshot
Structural Revisions of Natural Products with the Aid of the Structure Elucidator System
inferred← citeshttps://doi.org/10.1039/9781849734578-00419openalex-snapshot
Comparison of Systematic CASE Systems versus a Traditional Approach
inferred← citeshttps://doi.org/10.1039/b820693gopenalex-snapshot
Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
inferred← citeshttps://doi.org/10.1039/c002332aopenalex-snapshot
Structural revisions of natural products by Computer-Assisted Structure Elucidation (CASE) systems
inferred← citeshttps://doi.org/10.1039/c1cc11404bopenalex-snapshot
Single-molecule chemistry and physics explored by low-temperature scanning probe microscopy
inferred← citeshttps://doi.org/10.1039/c1ob05576copenalex-snapshot
Efficient and simple zinc-mediated synthesis of 3-amidoindoles
inferred← citeshttps://doi.org/10.1039/c1sc00190fopenalex-snapshot
Chiral phosphoric acid-catalysed Friedel–Crafts alkylation reaction of indoles with racemic spiro indolin-3-ones
inferred← citeshttps://doi.org/10.1039/c3cc41348aopenalex-snapshot
Synthesis of pseudo-indoxyl derivatives via sequential Cu-catalyzed SNAr and Smalley cyclization
inferred← citeshttps://doi.org/10.1039/c4cc03565hopenalex-snapshot
Flexible and practical synthesis of 3-oxyindoles through gold-catalyzed intermolecular oxidation of o-ethynylanilines
inferred← citeshttps://doi.org/10.1039/c4cc07743aopenalex-snapshot
Palladium-catalyzed selective aminoamidation and aminocyanation of alkenes using isonitrile as amide and cyanide sources
inferred← citeshttps://doi.org/10.1039/c4ob01039fopenalex-snapshot
Highly enantioselective synthesis of bisoxindoles with two vicinal quaternary stereocenters via Lewis base mediated addition of oxindoles to isatin-derived ketimines
inferred← citeshttps://doi.org/10.1039/c4ob01714eopenalex-snapshot
Fischer indolisation of N -(α-ketoacyl)anthranilic acids into 2-(indol-2-carboxamido)benzoic acids and 2-indolyl-3,1-benzoxazin-4-ones and their NMR study
inferred← citeshttps://doi.org/10.1039/c4ra01605jopenalex-snapshot
Unexpected TFA-catalyzed tandem reaction of benzo[d]oxazoles with 2-oxo-2-arylacetic acids: synthesis of 3-aryl-2H-benzo[b][1,4]oxazin-2-ones and cephalandole A
inferred← citeshttps://doi.org/10.1039/c6qo00698aopenalex-snapshot
Pd( ii )-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones
inferred← citeshttps://doi.org/10.1039/c6ra16877aopenalex-snapshot
Asymmetric Mannich reaction: highly enantioselective synthesis of 3-amino-oxindoles via chiral squaramide based H-bond donor catalysis
inferred← citeshttps://doi.org/10.1039/c7nj02246hopenalex-snapshot
Facile oxidative cyclization to access C2-quaternary 2-hydroxy-indolin-3-ones: synthetic studies towards matemone
inferred← citeshttps://doi.org/10.1039/c7ra10634copenalex-snapshot
Copper-catalyzed direct coupling of benzoxazin-2-ones with indoles for the synthesis of diverse 3-indolylbenzoxazin-2-ones: access to natural cephalandole A
inferred← citeshttps://doi.org/10.1039/c8qo00205copenalex-snapshot
Palladium-catalyzed asymmetric dearomative alkenylation of indoles through a reductive-Heck reaction
inferred← citeshttps://doi.org/10.1039/c9cc02956gopenalex-snapshot
Direct oxidative dearomatization of indoles: access to structurally diverse 2,2-disubstituted indolin-3-ones
inferred← citeshttps://doi.org/10.1039/c9gc04446aopenalex-snapshot
Direct C(sp 3 )–H acyloxylation of indolin-3-ones with carboxylic acids catalysed by KI
inferred← citeshttps://doi.org/10.1039/c9nj03620bopenalex-snapshot
From indoles to 3,3′-biindolin-2-ones: copper-catalyzed oxidative homocoupling of indoles
inferred← citeshttps://doi.org/10.1039/c9ob01870kopenalex-snapshot
Enantioselective construction of 3-substituted 3-amino-2-oxindoles containing an N , N -ketal skeleton via organocatalyzed aza-addition of isatin imines
inferred← citeshttps://doi.org/10.1039/c9ra02204jopenalex-snapshot
A facile approach to 2-alkoxyindolin-3-one and its application to the synthesis of N -benzyl matemone
inferred← citeshttps://doi.org/10.1039/d0cc05432aopenalex-snapshot
Organocatalytic asymmetric synthesis of arylindolyl indolin-3-ones with both axial and central chirality
inferred← citeshttps://doi.org/10.1039/d0ob02247kopenalex-snapshot
Chemoselective Cu-catalyzed synthesis of diverse N -arylindole carboxamides, β-oxo amides and N -arylindole-3-carbonitriles using diaryliodonium salts
inferred← citeshttps://doi.org/10.1039/d1ob01285aopenalex-snapshot
Total synthesis of the pseudoindoxyl class of natural products
inferred← citeshttps://doi.org/10.1039/d2cc02774gopenalex-snapshot
Gold-catalyzed redox cycloisomerization/nucleophilic addition/reduction: direct access to 2-phosphoryl indolin-3-ones
inferred← citeshttps://doi.org/10.1039/d2ob01063aopenalex-snapshot
Dearomative oxyphosphorylation of indoles enables facile access to 2,2-disubstituted indolin-3-ones
inferred← citeshttps://doi.org/10.1039/d2qo00048bopenalex-snapshot
Synthesis of 2-monosubstituted indolin-3-ones by cine -substitution of 3-azido-2-methoxyindolines
inferred← citeshttps://doi.org/10.1039/d3cc01390aopenalex-snapshot
Facile access to 2-hydroxy-2-substituted indole-3-ones via a copper-catalyzed oxidative cyclization of 2-arylethynylanilines
inferred← citeshttps://doi.org/10.1039/d3gc04154aopenalex-snapshot
Enantioselective cross-dehydrogenative coupling enabled by organocatalysis
inferred← citeshttps://doi.org/10.1039/d6nj01151aopenalex-snapshot
PPh 3 -Mediated synthesis of multifunctional indolin-3-one derivatives from 2-(ethynyl)nitrobenzenes and aryl ketones
inferred← citeshttps://doi.org/10.1039/d6nj01905fopenalex-snapshot
Recent advances in cascade cyclization of ortho -alkynyl and alkenyl isocyanides to access heterocyclic scaffolds
inferred← citeshttps://doi.org/10.1055/a-2341-9185openalex-snapshot
Metal-Free Synthesis of 2-Benzylideneindolin-3-ones via a Nucleophilic/Rearrangement/Azide–Alkene Cascade Reaction
inferred← citeshttps://doi.org/10.1055/s-0034-1379943openalex-snapshot
Organocatalytic Asymmetric Domino Michael/Henry Reaction of Indolin-3-ones with o-Formyl-β-nitrostyrenes
inferred← citeshttps://doi.org/10.1080/10286020.2015.1117452openalex-snapshot
Indole alkaloid glucosides from the roots of Isatis indigotica
inferred← citeshttps://doi.org/10.1101/2020.06.25.170639openalex-snapshot
The discovery of potential natural products for targeting SARS-CoV-2 spike protein by virtual screening
inferred← citeshttps://doi.org/10.1126/sciadv.aec9841openalex-snapshot
Photothermal catalysis versus thermal catalysis: A palladium-catalyzed intermolecular three-component C─H 1,3- N , O -difunctionalization
inferred← citeshttps://doi.org/10.1134/s1070428022100037openalex-snapshot
Synthesis of 1-Tosylspiro[3,1-benzoxazine-4,1′-cycloalkan]-2-imines
inferred← citeshttps://doi.org/10.1186/s13321-021-00559-3openalex-snapshot
Classifying natural products from plants, fungi or bacteria using the COCONUT database and machine learning
inferred← citeshttps://doi.org/10.1246/cl.2012.728openalex-snapshot
Isolation and Structure of a Novel Biindole Pigment Substituted with an Ethyl Group from a Metagenomic Library Derived from the Marine Sponge Halichondria okadai
inferred← citeshttps://doi.org/10.1248/cpb.c16-00315openalex-snapshot
Two New Alkaloids from the Roots of Baphicacanthus cusia
inferred← citeshttps://doi.org/10.17344/acsi.2017.3709openalex-snapshot
Microwave-assisted One-pot Efficient Synthesis of Functionalized 2-Oxo-2-phenylethylidenes-linked 2-Oxobenzo[1,4]oxazines and 2-Oxoquino[1,4]oxalines: Synthetic Applications, Antioxidant Activity, SAR and Cytotoxic Studies
inferred← citeshttps://doi.org/10.2174/9789815051995123030012openalex-snapshot
Effective Strategy of Drug Discovery from Marine Ecosystem
inferred← citeshttps://doi.org/10.26434/chemrxiv-2021-gxjgcopenalex-snapshot
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inferred← citeshttps://doi.org/10.33774/chemrxiv-2021-gxjgc-v2openalex-snapshot
Classifying Natural Products from Plants, Fungi or Bacteria using the COCONUT Database and Machine Learning
inferred← citeshttps://doi.org/10.3390/chemistry7020043openalex-snapshot
Molecular Iodine-Catalyzed Synthesis of 3,3-Disubstituted Isatins: Total Synthesis of Indole Alkaloid, 3,3-Dimethoxy-2-oxindole
inferred← citeshttps://doi.org/10.3390/ijms16023980openalex-snapshot
Isolation and Cytotoxicity Evaluation of the Chemical Constituents from Cephalantheropsis gracilis
inferred← citeshttps://doi.org/10.3390/md20010035openalex-snapshot
Saccharobisindole, Neoasterric Methyl Ester, and 7-Chloro-4(1H)-quinolone: Three New Compounds Isolated from the Marine Bacterium Saccharomonospora sp.
inferred← citeshttps://doi.org/10.3390/molecules21111605openalex-snapshot
Chemical Constituents of Phaius mishmensis
inferred← citeshttps://doi.org/10.3390/molecules25020419openalex-snapshot
Oxidative Dearomative Cross-Dehydrogenative Coupling of Indoles with Diverse C-H Nucleophiles: Efficient Approach to 2,2-Disubstituted Indolin-3-ones
inferred← citeshttps://doi.org/10.3390/ph16010105openalex-snapshot
Combining the In Silico and In Vitro Assays to Identify Strobilanthes cusia Kuntze Bioactives against Penicillin-Resistant Streptococcus pneumoniae
inferred← citeshttps://doi.org/10.4155/fmc.11.118openalex-snapshot
Marine Natural Products: A New Wave of Drugs?
inferred← citeshttps://doi.org/10.5897/jmpr10.012openalex-snapshot
Orchids : A review of uses in traditional medicine, its phytochemistry and pharmacology
inferred← citeshttps://doi.org/10.6023/cjoc202506013openalex-snapshot
PPh 3 -Mediated One-Pot Synthesis of Indolin-3-ones from 2-Alkynylnitrobenzenes and Indoles
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