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13C nuclear magnetic resonance spectra of amaryllidaceae alkaloids

https://doi.org/10.1039/p29730001180
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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/10.1002/chin.197333062openalex-snapshot
ChemInform Abstract: (13)C NUCLEAR MAGNETIC RESONANCE SPECTRA OF AMARYLLIDACEAE ALKALOIDS
inferred← citeshttps://doi.org/10.1002/ejoc.201500265openalex-snapshot
Total Synthesis of (±)‐8‐Oxo‐erythrinine, (±)‐8‐Oxo‐erythraline, and (±)‐Clivonine
inferred← citeshttps://doi.org/10.1002/mrc.1260231004openalex-snapshot
13C nuclear magnetic resonance spectra of amaryllidaceae alkaloids. I—alkaloids with the crinane skeleton
inferred← citeshttps://doi.org/10.1007/978-1-4757-2085-3_7openalex-snapshot
G
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The Use of Carbon-13 Nuclear Magnetic Resonance Spectroscopy in Natural Products Chemistry
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Lanthanide shift reagents in the chemistry of heterocyclic compounds. A review
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NMR investigation of alkaloids I.13C NMR spectra and stereochemistry of pentacyclic oxindole alkaloids of the heteroyohimbine group of the epiallo and allo series
inferred← citeshttps://doi.org/10.1016/0022-2313(91)90138-lopenalex-snapshot
Fluorescence properties of heterocyclic aromatic diether derivatives and their polymers
inferred← citeshttps://doi.org/10.1016/0031-9422(81)84053-8openalex-snapshot
Alkaloids of Crinum pratense
inferred← citeshttps://doi.org/10.1016/0031-9422(88)80457-6openalex-snapshot
Isocraugsodine, an n-arylidenephenethylamine from Crinum asiaticum and its e-z isomerism
inferred← citeshttps://doi.org/10.1016/0031-9422(89)80322-xopenalex-snapshot
2-O-acetyl chlidanthine; An alkaloid from Haemanthus multiflorus
inferred← citeshttps://doi.org/10.1016/0031-9422(91)83751-6openalex-snapshot
Alkaloid N-oxides from Lycoris sanguinea
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00375-hopenalex-snapshot
Further alkaloids from Brunsvigia josephinae
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104567openalex-snapshot
Alkaloids of Zephyranthes citrina (Amaryllidaceae) and their implication to Alzheimer's disease: Isolation, structural elucidation and biological activity
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.10.061openalex-snapshot
New lycorine-type alkaloid from Lycoris traubii and evaluation of antitrypanosomal and antimalarial activities of lycorine derivatives
inferred← citeshttps://doi.org/10.1016/j.phymed.2007.12.001openalex-snapshot
Screening for cytotoxic activity of extracts and isolated alkaloids from bulbs of Hippeastrum vittatum
inferred← citeshttps://doi.org/10.1016/j.sajb.2021.09.034openalex-snapshot
Chemical profile and biological activity of Crinum americanum L. (Amaryllidaceae)
inferred← citeshttps://doi.org/10.1016/j.tet.2010.04.132openalex-snapshot
An oxidative coupling for the synthesis of arylated quaternary stereocentres and its application in the total synthesis of powelline and buphanidrine
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)98566-2openalex-snapshot
Relative configuration of the alkaloid augustine
inferred← citeshttps://doi.org/10.1016/s0031-9422(97)01024-8openalex-snapshot
Biosynthesis of the amaryllidaceae alkaloid Galanthaminefn2fn2Dedicatedto Prof. T. Hartmann, Braunschweig, on the occasion of his 60th birthday.
inferred← citeshttps://doi.org/10.1016/s0099-9598(08)60208-4openalex-snapshot
Chapter 3 The Amaryllidaceae Alkaloids
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/10.1016/s1572-5995(97)80034-8openalex-snapshot
Narcissus alkaloids
inferred← citeshttps://doi.org/10.1016/s1876-0813(08)60275-4openalex-snapshot
Chapter 3 The Amaryllidaceae Alkaloids
inferred← citeshttps://doi.org/10.1021/ja910184jopenalex-snapshot
Total Synthesis of the Lycorenine-Type Amaryllidaceae Alkaloid (±)-Clivonine via a Biomimetic Ring-Switch from a Lycorine-Type Progenitor
inferred← citeshttps://doi.org/10.1021/ol1000654openalex-snapshot
Total Synthesis of (±)-Powelline and (±)-Buphanidrine
inferred← citeshttps://doi.org/10.1039/c0ob00895hopenalex-snapshot
Total synthesis of the Amaryllidaceae alkaloid clivonine
inferred← citeshttps://doi.org/10.1039/c9ob00166bopenalex-snapshot
Selective synthesis of spirooxindoles via a two-step reaction of N -phenacylpyridinium bromide, 1,3-indanedione and N -alkylisations
inferred← citeshttps://doi.org/10.1076/phbi.34.3.194.13207openalex-snapshot
Alkaloids of Sternbergia clusiana and their Analgesic Effects
inferred← citeshttps://doi.org/10.1111/irv.12035openalex-snapshot
Amaryllidaceae alkaloids inhibit nuclear‐to‐cytoplasmic export of ribonucleoprotein (RNP) complex of highly pathogenic avian influenza virus H5N1
inferred← citeshttps://doi.org/10.1177/1934578x1100600208openalex-snapshot
Chemical Constituents of Lycoris albiflora and their Cytotoxic Activities
inferred← citeshttps://doi.org/10.3987/com-08-s(f)92openalex-snapshot
Two New Alkaloids from Bulbs of Lycoris squamigera
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