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Lycopodatines A−C, C16N Alkaloids fromLycopodiuminundatum
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3773(20020517)41:10<1783::aid-anie1783>3.0.co;2-iopenalex-snapshot
A Short Synthesis of (±)-13-Deoxyserratine
inferredcites →https://doi.org/10.1002/1521-3773(20021104)41:21<4093::aid-anie4093>3.0.co;2-iopenalex-snapshot
Highly Selective Disaccharide Recognition by a Tricyclic Octaamide Cage
inferredcites →https://doi.org/10.1002/bscb.19710800110openalex-snapshot
Some Constituents of Lycopodium Inundatum L
inferredcites →https://doi.org/10.1002/cjce.5450640519openalex-snapshot
Correlations for prediction of diffusion in liquids
inferredcites →https://doi.org/10.1016/j.tet.2003.09.106openalex-snapshot
New phlegmarane-type, cernuane-type, and quinolizidine alkaloids from two species of Lycopodium
inferredcites →https://doi.org/10.1016/s0040-4020(02)00520-3openalex-snapshot
Lyconesidines A–C, new alkaloids from Lycopodium chinense
inferredcites →https://doi.org/10.1016/s0040-4020(03)00545-3openalex-snapshot
Senepodines B–E, new C22N2 alkaloids from Lycopodium chinense
inferredcites →https://doi.org/10.1016/s1099-4831(05)61001-2openalex-snapshot
The Lycopodium Alkaloids
inferredcites →https://doi.org/10.1021/ar9800892openalex-snapshot
Chemistry, Pharmacology, and Clinical Efficacy of the Chinese Nootropic Agent Huperzine A
inferredcites →https://doi.org/10.1021/ja00060a064openalex-snapshot
First total synthesis of Lycopodium alkaloids of the magellanane group. Enantioselective total syntheses of (-)-magellanine and (+)-magellaninone
inferredcites →https://doi.org/10.1021/ja953735qopenalex-snapshot
A Classical Paradigm of Alkaloid Biogenesis Revisited: Acetonedicarboxylic Acid as a Biosynthetic Precursor of Lycopodine
inferredcites →https://doi.org/10.1021/jo034294topenalex-snapshot
Himeradine A, a Novel C27N3-Type Alkaloid from Lycopodium chinense
inferredcites →https://doi.org/10.1021/ol035560sopenalex-snapshot
Sieboldine A, a Novel Tetracyclic Alkaloid from Lycopodium sieboldii, Inhibiting Acetylcholinesterase
inferredcites →https://doi.org/10.1021/ol048621aopenalex-snapshot
Nankakurine A, a Novel C16N2-Type Alkaloid from Lycopodium hamiltonii
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.2022.113553zenodo-depositor-declared
Phlegcarines A-C, three Lycopodium alkaloids from Phlegmariurus carinatus (Desv. ex Poir.) Ching
inferred← citeshttps://doi.org/10.1002/chem.201702428openalex-snapshot
α‐Quaternary Mannich Bases through Copper‐Catalyzed Amination‐Induced 1,2‐Rearrangement of Allylic Alcohols
inferred← citeshttps://doi.org/10.1002/hlca.201400015openalex-snapshot
Lycopodium Alkaloids from Huperzia serrata
inferred← citeshttps://doi.org/10.1007/978-3-030-97415-2_10-1openalex-snapshot
Bioactive Compounds of Pteridophytes
inferred← citeshttps://doi.org/10.1007/978-3-031-23243-5_10openalex-snapshot
Bioactive Compounds of Pteridophytes
inferred← citeshttps://doi.org/10.1007/s11101-021-09746-4openalex-snapshot
The traditional uses, secondary metabolites, and pharmacology of Lycopodium species
inferred← citeshttps://doi.org/10.1007/s13659-013-0015-xopenalex-snapshot
New Lycopodium alkaloids from Lycopodium obscurum
inferred← citeshttps://doi.org/10.1007/s13659-014-0030-6openalex-snapshot
Carinatines A and B, Lycopodium Alkaloids from Phlegmariurus carinatus
inferred← citeshttps://doi.org/10.1016/j.bmc.2006.12.005openalex-snapshot
Carinatumins A–C, new alkaloids from Lycopodium carinatum inhibiting acetylcholinesterase
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.04.044openalex-snapshot
Lycoparins A–C, new alkaloids from Lycopodium casuarinoides inhibiting acetylcholinesterase
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.07.003openalex-snapshot
Annotinolide F and lycoannotines A–I, further Lycopodium alkaloids from Lycopodium annotinum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.09.001openalex-snapshot
Three Lycopodium alkaloids from Thai club mosses
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00815openalex-snapshot
Lycosquarrines A–R, Lycopodium Alkaloids from Phlegmariurus squarrosus
inferred← citeshttps://doi.org/10.1021/ol802005nopenalex-snapshot
Tandem Aziridination/Rearrangement Reaction of Allylic Alcohols: An Efficient Approach to 2-Quaternary Mannich Bases
inferred← citeshttps://doi.org/10.1134/s1234567813040101openalex-snapshot
LYCOPODIELLA INUNDATA И SELAGINELLA SELAGINOIDES В ВОЛОГОДСКОЙ ОБЛАСТИ, "БОТАНИЧЕСКИЙ ЖУРНАЛ"
inferred← citeshttps://doi.org/10.3184/174751912x13249872110014openalex-snapshot
A New Lycopodine Alkaloid from Huperzia Serrata
inferred← citeshttps://doi.org/10.3987/com-06-10868openalex-snapshot
Nankakurine B, a New Alkaloid from Lycopodium hamiltonii and Revised Stereostructure of Nankakurine A
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