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Total Syntheses of Lycopodium and Monoterpenoid Indole Alkaloids Based on Biosynthesis-Inspired Strategies
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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/anie.201103550openalex-snapshot
Asymmetric Total Synthesis of a Pentacyclic Lycopodium Alkaloid: Huperzine‐Q
inferredcites →https://doi.org/10.1002/anie.201802610openalex-snapshot
Bioinspired Oxidative Cyclization of the Geissoschizine Skeleton for the Total Synthesis of (−)‐17‐nor‐Excelsinidine
inferredcites →https://doi.org/10.1002/asia.201000538openalex-snapshot
Seven New Monoterpenoid Indole Alkaloids from Gelsemium elegans
inferredcites →https://doi.org/10.1002/chem.201303975openalex-snapshot
Heathcock‐Inspired Strategies for the Synthesis of Fawcettimine‐Type Lycopodium Alkaloids
inferredcites →https://doi.org/10.1002/chin.199816307openalex-snapshot
ChemInform Abstract: Monoterpenoid Indole Alkaloid Syntheses Utilizing Biomimetic Reactions
inferredcites →https://doi.org/10.1007/128_2011_126openalex-snapshot
Lycopodium Alkaloids: Isolation and Asymmetric Synthesis
inferredcites →https://doi.org/10.1007/s11418-009-0334-8openalex-snapshot
Kopsiyunnanines F and isocondylocarpines: new tubotaiwine-type alkaloids from Yunnan Kopsia arborea
inferredcites →https://doi.org/10.1007/s12013-014-0479-2openalex-snapshot
Apoptotic Effect of Koumine on Human Breast Cancer Cells and the Mechanism Involved
inferredcites →https://doi.org/10.1016/b978-0-12-407774-4.00001-7openalex-snapshot
Lycopodium Alkaloids – Synthetic Highlights and Recent Developments
inferredcites →https://doi.org/10.1016/j.jep.2014.01.003openalex-snapshot
Medicinal plants of the genus Gelsemium (Gelsemiaceae, Gentianales)—A review of their phytochemistry, pharmacology, toxicology and traditional use
inferredcites →https://doi.org/10.1016/j.pbb.2012.02.009openalex-snapshot
Effects of koumine, an alkaloid of Gelsemium elegans Benth., on inflammatory and neuropathic pain models and possible mechanism with allopregnanolone
inferredcites →https://doi.org/10.1016/j.tet.2008.12.067openalex-snapshot
A divergent approach for the total syntheses of cernuane-type and quinolizidine-type Lycopodium alkaloids
inferredcites →https://doi.org/10.1016/j.tet.2011.05.026openalex-snapshot
Six new monoterpenoid indole alkaloids from the aerial part of Gelsemium elegans
inferredcites →https://doi.org/10.1016/j.tet.2014.11.038openalex-snapshot
Total synthesis of (±)-lycoposerramine-R, a novel skeletal type of Lycopodium alkaloid
inferredcites →https://doi.org/10.1016/j.tet.2016.08.082openalex-snapshot
Kopsiyunnanines L and M, Strychnos-related monoterpenoid indole alkaloids from Yunnan Kopsia arborea
inferredcites →https://doi.org/10.1016/j.tetlet.2008.07.145openalex-snapshot
Two novel indole alkaloids, Kopsiyunnanines A and B, from a Yunnan Kopsia
inferredcites →https://doi.org/10.1016/j.tetlet.2012.09.078openalex-snapshot
Chemical conversion of strychnine into kopsiyunnanine-I, a new hexacyclic indole alkaloid from Yunnan Kopsia arborea
inferredcites →https://doi.org/10.1016/j.tetlet.2015.12.029openalex-snapshot
Total synthesis of conolidine and apparicine
inferredcites →https://doi.org/10.1016/j.tetlet.2018.04.041openalex-snapshot
Antimicrobial indole alkaloids with adductive C9 aromatic unit from Gelsemium elegans
inferredcites →https://doi.org/10.1016/j.tetlet.2018.12.007openalex-snapshot
Concise asymmetric total synthesis of lycopodine and flabelliformine via cascade cyclization reaction
inferredcites →https://doi.org/10.1016/s0040-4020(01)89296-6openalex-snapshot
A biomimetic synthesis of a new skeletal Gelsemium alkaloid, 11-methoxy-19(R)-hydroxygelselegine
inferredcites →https://doi.org/10.1016/s0040-4039(00)61787-2openalex-snapshot
Geissoschizine revisited - definite proof of its stereostructure.
inferredcites →https://doi.org/10.1016/s0099-9598(08)60015-2openalex-snapshot
Chapter 1 Gelsemium Alkaloids
inferredcites →https://doi.org/10.1016/s1099-4831(05)61001-2openalex-snapshot
The Lycopodium Alkaloids
inferredcites →https://doi.org/10.1016/s1099-4831(08)00201-0openalex-snapshot
Chapter 1 Alkaloids of Kopsia
inferredcites →https://doi.org/10.1016/s1099-4831(08)60049-8openalex-snapshot
Chapter 11 Monoterpenoid Indole Alkaloid Syntheses Utilizing Biomimetic Reactions
inferredcites →https://doi.org/10.1021/acs.joc.9b00586openalex-snapshot
Asymmetric Total Synthesis of Fawcettimine-Type Lycopodium Alkaloid, Lycopoclavamine-A
inferredcites →https://doi.org/10.1021/acs.orglett.6b00661openalex-snapshot
Asymmetric Total Synthesis of Sarpagine-Related Indole Alkaloids Hydroxygardnerine, Hydroxygardnutine, Gardnerine, (E)-16-epi-Normacusine B, and Koumine
inferredcites →https://doi.org/10.1021/acs.orglett.6b01704openalex-snapshot
Asymmetric Total Synthesis of Kopsiyunnanine K, a Monoterpenoid Indole Alkaloid with a Rearranged Skeleton
inferredcites →https://doi.org/10.1021/acs.orglett.7b01076openalex-snapshot
Asymmetric Total Synthesis of Pentacyclic Indole Alkaloid Andranginine and Absolute Configuration of Natural Product Isolated from Kopsia arborea
inferredcites →https://doi.org/10.1021/acs.orglett.9b01084openalex-snapshot
Total Syntheses of Pleiocarpamine, Normavacurine, and C-Mavacurine
inferredcites →https://doi.org/10.1021/acs.orglett.9b02703openalex-snapshot
Total Synthesis of (−)-14-Hydroxygelsenicine and Six Biogenetically Related Gelsemium Alkaloids
inferredcites →https://doi.org/10.1021/ar50029a002openalex-snapshot
Biosynthesis of the indole alkaloids
inferredcites →https://doi.org/10.1021/ja00060a078openalex-snapshot
Biosynthesis of lycopodine: incorporation of acetate via an intermediate with C2v symmetry
inferredcites →https://doi.org/10.1021/ja00184a086openalex-snapshot
Total synthesis of (+)-koumine, (+)-taberpsychine, and (+)-koumidine
inferredcites →https://doi.org/10.1021/ja00368a024openalex-snapshot
Total synthesis of lycopodium alkaloids: (.+-.)-lycopodine, (.+-.)-lycodine, and (.+-.)-lycodoline
inferredcites →https://doi.org/10.1021/ja507016gopenalex-snapshot
Biogenetically Inspired Total Syntheses of Lycopodium Alkaloids, (+)-Flabellidine and (−)-Lycodine
inferredcites →https://doi.org/10.1021/jo0483825openalex-snapshot
Structure Elucidation and Synthesis of Lycoposerramine-B, a Novel Oxime-ContainingLycopodiumAlkaloid fromLycopodium serratumThunb.
inferredcites →https://doi.org/10.1021/jo9018182openalex-snapshot
Asymmetric Total Syntheses of Cyclic Nitrone-Containing Phlegmarine-Type Lycopodium Alkaloids, Lycoposerramines-X and -Z
inferredcites →https://doi.org/10.1021/jo991333lopenalex-snapshot
An Easy Access to 2,6-Dihydroxy-9-azabicyclo[3.3.1]nonane, a Versatile Synthon
inferredcites →https://doi.org/10.1021/np060016oopenalex-snapshot
Isolation of Gelsedine-Type Indole Alkaloids from Gelsemium elegans and Evaluation of the Cytotoxic Activity of Gelsemium Alkaloids for A431 Epidermoid Carcinoma Cells
inferredcites →https://doi.org/10.1021/np800489eopenalex-snapshot
Rhazinilam and Quebrachamine Derivatives from Yunnan Kopsia arborea
inferredcites →https://doi.org/10.1021/ol0344725openalex-snapshot
Structure Reinvestigation of Gelsemoxonine, a Constituent of Gelsemium elegans, Reveals a Novel, Azetidine-Containing Indole Alkaloid
inferredcites →https://doi.org/10.1021/ol061062iopenalex-snapshot
Four Novel Gelsenicine-Related Oxindole Alkaloids from the Leaves of Gelsemium elegans Benth.
inferredcites →https://doi.org/10.1021/ol502265qopenalex-snapshot
Asymmetric Total Synthesis of Novel Pentacyclic Indole Alkaloid, Kopsiyunnanine E, Isolated from Kopsia arborea
inferredcites →https://doi.org/10.1021/ol701871vopenalex-snapshot
Asymmetric Total Syntheses of Two Phlegmarine-Type Alkaloids, Lycoposerramines-V and -W, Newly Isolated fromLycopodium serratum
inferredcites →https://doi.org/10.1021/ol800574vopenalex-snapshot
First Asymmetric Total Syntheses of Cernuane-Type Lycopodium Alkaloids, Cernuine, and Cermizine D
inferredcites →https://doi.org/10.1021/ol902437topenalex-snapshot
First Asymmetric Total Syntheses of Fawcettimine-Type Lycopodium Alkaloids, Lycoposerramine-C and Phlegmariurine-A
inferredcites →https://doi.org/10.1039/a902278copenalex-snapshot
Biomimetic synthesis of alkaloids (1980 to 1999)
inferredcites →https://doi.org/10.1039/b705909bopenalex-snapshot
Recent advances in biomimetic natural product synthesis
inferredcites →https://doi.org/10.1039/b819925fopenalex-snapshot
Biogenetically inspired syntheses of alkaloid natural products
inferredcites →https://doi.org/10.1039/b923918aopenalex-snapshot
Determination of absolute configuration of trimeric indole alkaloid, psychotrimine, by first asymmetric total synthesis
inferredcites →https://doi.org/10.1039/c5ob00827aopenalex-snapshot
The first asymmetric total synthesis of lycoposerramine-R
inferredcites →https://doi.org/10.1055/s-0032-1316680openalex-snapshot
Syntheses of Fawcettimine-Type Lycopodium Alkaloids Utilizing the Pauson-Khand Reaction
inferredcites →https://doi.org/10.1055/s-2007-971416openalex-snapshot
A Plausible Biogenetic Proposal for Koumine
inferredcites →https://doi.org/10.1248/bpb.b13-00843openalex-snapshot
Anti-allodynic and Neuroprotective Effects of Koumine, a Benth Alkaloid, in a Rat Model of Diabetic Neuropathy
inferredcites →https://doi.org/10.1248/cpb.58.961openalex-snapshot
Two New Aspidosperma Indole Alkaloids from Yunnan Kopsia arborea
inferredcites →https://doi.org/10.2183/pjab.74.159openalex-snapshot
A chemical study on "Yakatsu" stored in Shosoin repository. Isolation and characterization of four indole alkaloids from a 1250 year-old sample of the Chinese toxic medicine.
inferredcites →https://doi.org/10.5059/yukigoseikyokaishi.60.350openalex-snapshot
Current Topics in the Biomimetic Alkaloid Syntheses.
inferredcites →https://doi.org/10.5059/yukigoseikyokaishi.68.457openalex-snapshot
Isolation, Structure Elucidation, and Asymmetric Synthesis of Biologically Active New Lycopodium Alkaloids
inferredcites →https://doi.org/10.5059/yukigoseikyokaishi.73.1072openalex-snapshot
Recent Progress in Total Synthesis of Lycopodium Alkaloids
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.2021.113056zenodo-depositor-declared
Serratene triterpenoids from Lycopodium cernuum L. as α-glucosidase inhibitors: Identification, structure–activity relationship and molecular docking studies
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00623openalex-snapshot
Huperserratines A and B, Two Macrocyclic Lycopodium Alkaloids with an Unusual Skeleton from Huperzia serrata
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02672openalex-snapshot
Asymmetric Total Synthesis and Structure Elucidation of Huperzine H
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00133openalex-snapshot
Asymmetric Total Synthesis of Senepodine F
inferred← citeshttps://doi.org/10.1021/jacs.1c00457openalex-snapshot
Bioinspired Diversification Approach Toward the Total Synthesis of Lycodine-Type Alkaloids
inferred← citeshttps://doi.org/10.1039/d4qo01122hopenalex-snapshot
Total synthesis of (–)-deglycocadambine
inferred← citeshttps://doi.org/10.3390/ijms231911860openalex-snapshot
Effects of Dietary Koumine on Growth Performance, Intestinal Morphology, Microbiota, and Intestinal Transcriptional Responses of Cyprinus carpio
inferred← citeshttps://doi.org/10.3390/plants14152395openalex-snapshot
HPLC-ESI-HRMS/MS-Based Metabolite Profiling and Bioactivity Assessment of Catharanthus roseus
inferred← citeshttps://doi.org/10.3987/com-20-14351openalex-snapshot
Elucidation of Absolute Configuration of Ophiorrhiside A by Comparison of ECD Spectra with That of Model Chiral Compound Having a 1,2,3,4-Tetrahydro-β-carbolin-3-one Skeleton
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.79.596openalex-snapshot
What I Learned from Exploratory Research on Alkaloids
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