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Lycopodium Alkaloids: Isolation and Asymmetric Synthesis

https://doi.org/10.1007/128_2011_126
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What this work says

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

inferredcites →https://doi.org/10.1002/0471264180.os079.22openalex-snapshot
Preparation of Secondary Amines From Primary Amines Via 2‐Nitrobenzenesulfonamides: N‐(4‐Methoxybenzyl)‐3‐Phenylpropylamine
inferredcites →https://doi.org/10.1002/1521-3773(20020517)41:10<1790::aid-anie1790>3.0.co;2-yopenalex-snapshot
Direct Organo-Catalytic Asymmetricα-Amination of Aldehydes—A Simple Approach to Optically Activeα-Amino Aldehydes,α-Amino Alcohols, andα-Amino Acids
inferredcites →https://doi.org/10.1002/anie.200702695openalex-snapshot
Total Synthesis of (+)‐Fawcettimine
inferredcites →https://doi.org/10.1002/anie.200800522openalex-snapshot
Total Synthesis of (+)‐Fawcettidine
inferredcites →https://doi.org/10.1002/anie.200907248openalex-snapshot
Total Synthesis of (+)‐Clavolonine, (−)‐Deacetylfawcettiine, and (+)‐Acetylfawcettiine
inferredcites →https://doi.org/10.1002/chin.199205061openalex-snapshot
ChemInform Abstract: Investigations on 1,2‐, 1,3‐, and 1,4‐Asymmetric Induction in Intramolecular Reformatsky Reactions Promoted by Samarium(II) Iodide.
inferredcites →https://doi.org/10.1002/ejoc.201000667openalex-snapshot
Concise Total Synthesis of (±)‐Lycodine
inferredcites →https://doi.org/10.1002/hlca.200800327openalex-snapshot
A New Lycopodium Alkaloid, Lycoposerramine‐R, with a Novel Skeleton and Three New Fawcettimine‐Related Alkaloids from Lycopodium serratum
inferredcites →https://doi.org/10.1002/jlac.18812080308openalex-snapshot
Lycopodin, das erste Alkaloïd der Gefässkryptogamen
inferredcites →https://doi.org/10.1016/0022-328x(88)89064-8openalex-snapshot
Chiral synthesis via organoboranes
inferredcites →https://doi.org/10.1016/0040-4039(95)01316-aopenalex-snapshot
2- and 4-Nitrobenzenesulfonamides: Exceptionally versatile means for preparation of secondary amines and protection of amines
inferredcites →https://doi.org/10.1016/j.bmc.2006.05.028openalex-snapshot
Lycopladines B–D and lyconadin B, new alkaloids from Lycopodium complanatum
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/j.tet.2005.01.011openalex-snapshot
Complanadine B, obscurumines A and B, new alkaloids from two species of Lycopodium
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/s0040-4039(00)75730-3openalex-snapshot
Serratinine: A novel skeletal lycopodium alkaloid
inferredcites →https://doi.org/10.1016/s0040-4039(00)94494-0openalex-snapshot
Preparation and rearrangement of 2-allyloxyethyl aryl sulfoxides; a mercury-free claisen sequence
inferredcites →https://doi.org/10.1016/s0040-4039(01)97681-6openalex-snapshot
The crystal structure of 13-acetyl-8-p-bromo-benzoyl serratinine: the revised configuration of C4-N bond of serratinine
inferredcites →https://doi.org/10.1016/s0040-4039(02)02026-9openalex-snapshot
Seven new Lycopodium alkaloids, lycoposerramines-C, -D, -E, -P, -Q, -S, and -U, from Lycopodium serratum Thunb.
inferredcites →https://doi.org/10.1016/s0099-9598(08)60196-0openalex-snapshot
Chapter 5 Lycopodium Alkaloids
inferredcites →https://doi.org/10.1016/s1876-0813(08)60017-2openalex-snapshot
Chapter 23 The Lycopodium Alkaloids
inferredcites →https://doi.org/10.1016/s1876-0813(08)60090-1openalex-snapshot
Chapter 47 The Lycopodium Alkaloids
inferredcites →https://doi.org/10.1021/acs.orglett.7b01633openalex-snapshot
Total Synthesis of Huperzine Q
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/cr00039a007openalex-snapshot
Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
inferredcites →https://doi.org/10.1021/cr950019yopenalex-snapshot
Sequencing Reactions with Samarium(II) Iodide
inferredcites →https://doi.org/10.1021/ja00021a033openalex-snapshot
Investigations on 1,2-, 1,3-, and 1,4-asymmetric induction in intramolecular Reformatskii reactions promoted by samarium(II) iodide
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/ja00276a062openalex-snapshot
Total synthesis of (.+-.)-fawcettimine (Burnell's base A)
inferredcites →https://doi.org/10.1021/ja00452a040openalex-snapshot
Hydroboration. 46. The regio- and stereochemistry of the hydroboration of representative cyclic olefins with 9-borabicyclo[3.3.1]nonane
inferredcites →https://doi.org/10.1021/ja021111wopenalex-snapshot
Acetylcholinesterase Complexed with Bivalent Ligands Related to Huperzine A: Experimental Evidence for Species-Dependent Protein−Ligand Complementarity
inferredcites →https://doi.org/10.1021/ja0261325openalex-snapshot
Direct Catalytic Asymmetric α-Amination of Aldehydes
inferredcites →https://doi.org/10.1021/ja026412kopenalex-snapshot
Direct l -Proline-Catalyzed Asymmetric α-Amination of Ketones
inferredcites →https://doi.org/10.1021/ja064106ropenalex-snapshot
Enantioselective Transfer Aminoallylation: Synthesis of Optically Active Homoallylic Primary Amines
inferredcites →https://doi.org/10.1021/ja070336+openalex-snapshot
Total Syntheses of (+)-Lyconadin A and (−)-Lyconadin B
inferredcites →https://doi.org/10.1021/ja101893bopenalex-snapshot
Total Synthesis of (+)-Complanadine A Using an Iridium-Catalyzed Pyridine C−H Functionalization
inferredcites →https://doi.org/10.1021/ja101956xopenalex-snapshot
Synthesis of (+)-Complanadine A, an Inducer of Neurotrophic Factor Excretion
inferredcites →https://doi.org/10.1021/ja103666nopenalex-snapshot
Total Synthesis of (+)-Sieboldine A
inferredcites →https://doi.org/10.1021/ja104575hopenalex-snapshot
Total Synthesis of (+)-Fastigiatine
inferredcites →https://doi.org/10.1021/ja107533mopenalex-snapshot
Synthesis of the Lycopodium Alkaloid (+)-Lycoflexine
inferredcites →https://doi.org/10.1021/ja109516fopenalex-snapshot
Concise Total Synthesis of (+)-Lyconadin A
inferredcites →https://doi.org/10.1021/ja8028069openalex-snapshot
Unified Strategy for the Synthesis of the “Miscellaneous” Lycopodium Alkaloids: Total Synthesis of (±)-Lyconadin A
inferredcites →https://doi.org/10.1021/ja803613wopenalex-snapshot
Enantioselective Total Synthesis of Lycopodine
inferredcites →https://doi.org/10.1021/ja804624uopenalex-snapshot
Enantioselective Total Syntheses of Nankakurines A and B: Confirmation of Structure and Establishment of Absolute Configuration
inferredcites →https://doi.org/10.1021/ja900536dopenalex-snapshot
Total Synthesis of the Lycopodium Alkaloid (+)-Serratezomine A
inferredcites →https://doi.org/10.1021/jo00195a052openalex-snapshot
B-Allyldiisocaranylborane: a new, remarkable enantioselective allylborating agent for prochiral aldehydes. Synthesis of homoallylic alcohols approaching 100% enantiomeric purities
inferredcites →https://doi.org/10.1021/jo00268a015openalex-snapshot
Total synthesis of (.+-.)-fawcettimine
inferredcites →https://doi.org/10.1021/jo00354a003openalex-snapshot
Chiral synthesis via organoboranes. 6. Asymmetric allylboration via chiral allyldialkylboranes. Synthesis of homoallylic alcohols with exceptionally high enantiomeric excess
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/jo062067wopenalex-snapshot
Total Synthesis of (−)-Senepodine G and (−)-Cermizine C
inferredcites →https://doi.org/10.1021/jo100916xopenalex-snapshot
Development of an Enantioselective Route toward the Lycopodium Alkaloids: Total Synthesis of Lycopodine
inferredcites →https://doi.org/10.1021/jo101619dopenalex-snapshot
Total Synthesis of (+)-Nankakurines A and B and (±)-5-epi-Nankakurine A
inferredcites →https://doi.org/10.1021/jo702136bopenalex-snapshot
Stereoselective Total Syntheses of Three Lycopodium Alkaloids, (−)-Magellanine, (+)-Magellaninone, and (+)-Paniculatine, Based on Two Pauson−Khand Reactions
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/jo982059iopenalex-snapshot
Synthesis of Enantiomerically Pure N-tert-Butanesulfinyl Imines (tert-Butanesulfinimines) by the Direct Condensation of tert-Butanesulfinamide with Aldehydes and Ketones
inferredcites →https://doi.org/10.1021/ol0167762openalex-snapshot
A New Type of Lycopodium Alkaloid, Lycoposerramine-A, fromLycopodiumserratumThunb
inferredcites →https://doi.org/10.1021/ol100273popenalex-snapshot
Concise Total Synthesis of (±)-Lycopladine A
inferredcites →https://doi.org/10.1021/ol100823topenalex-snapshot
Methoxypyridines in the Synthesis of Lycopodium Alkaloids: Total Synthesis of (±)-Lycoposerramine R
inferredcites →https://doi.org/10.1021/ol1012444openalex-snapshot
Total Synthesis of (−)-8-Deoxyserratinine via an Efficient Helquist Annulation and Double N-Alkylation Reaction
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/ol9022408openalex-snapshot
Total Synthesis of (−)-Huperzine A
inferredcites →https://doi.org/10.1021/ol902389eopenalex-snapshot
Total Synthesis of (−)-Lycoperine A
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/10.1021/ol902455yopenalex-snapshot
Concise Total Syntheses of the Lycopodium Alkaloids (±)-Nankakurines A and B via Luciduline
inferredcites →https://doi.org/10.1039/b311203aopenalex-snapshot
Ns strategies: a highly versatile synthetic method for amines
inferredcites →https://doi.org/10.1039/b409720nopenalex-snapshot
The Lycopodium alkaloids
inferredcites →https://doi.org/10.1039/c2971000036aopenalex-snapshot
A cobalt induced cleavage reaction and a new series of arenecobalt carbonyl complexes
inferredcites →https://doi.org/10.1039/np9910800455openalex-snapshot
The lycopodium alkaloids
inferredcites →https://doi.org/10.1139/cjr48b-001openalex-snapshot
THE ALKALOIDS OF LYCOPODIUM SPECIES: X. LYCOPODIUM CERNUUM L.
inferredcites →https://doi.org/10.1139/v67-077openalex-snapshot
The alkaloids of Lycopodium cernuum L. I. The structures of cernuine and lycocernuine
inferredcites →https://doi.org/10.1139/v86-137openalex-snapshot
The structures of huperzine A and B, two new alkaloids exhibiting marked anticholinesterase activity
inferredcites →https://doi.org/10.1248/cpb.16.82openalex-snapshot
Serratinine ; A Novel Skeletal Lycopodium Alkaloid
inferredcites →https://doi.org/10.1248/cpb.23.1511openalex-snapshot
Total synthesis of the lycopodium alkaloid dl-serratinine.
inferredcites →https://doi.org/10.15227/orgsyn.079.0186openalex-snapshot
PREPARATION OF SECONDARY AMINES FROM PRIMARY AMINES VIA 2-NITROBENZENESULFONAMIDES: N-(4-METHOXYBENZYL)-3-PHENYLPROPYLAMINE
inferredcites →https://doi.org/10.3987/com-06-s(o)16openalex-snapshot
Three New Phlegmarine-Type Lycopodium Alkaloids, Lycoposerramines-X, -Y and -Z, Having a Nitrone Residue, from Lycopodium serratum
inferredcites →https://doi.org/10.3987/rev-08-sr(f)6openalex-snapshot
The Lycopodium Alkaloids
inferredcites →https://doi.org/10.5059/yukigoseikyokaishi.61.1166openalex-snapshot
Pauson-Khand Reaction of Enynes Bearing exo-Olefin and Its Application to Total Synthesis of Lycopodium Alkaloid, Magellanine

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/10.1016/j.phytochem.2022.113553zenodo-depositor-declared
Phlegcarines A-C, three Lycopodium alkaloids from Phlegmariurus carinatus (Desv. ex Poir.) Ching
inferred← citeshttps://doi.org/10.1002/9781118754085.ch11openalex-snapshot
Ornithine and Lysine Alkaloids
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A Concise Total Synthesis of (+)‐Paniculatine
inferred← citeshttps://doi.org/10.1002/ajoc.201900262openalex-snapshot
Progress towards the Total Syntheses of Lycopodium Alkaloid, Lycopladine A
inferred← citeshttps://doi.org/10.1002/ange.201103550openalex-snapshot
Asymmetric Total Synthesis of a Pentacyclic Lycopodium Alkaloid: Huperzine‐Q
inferred← citeshttps://doi.org/10.1002/ange.201106753openalex-snapshot
Total Syntheses of Lycopodium Alkaloids (+)‐Fawcettimine, (+)‐Fawcettidine, and (−)‐8‐Deoxyserratinine
inferred← citeshttps://doi.org/10.1002/ange.201205711openalex-snapshot
Potentially Biomimetic Total Synthesis and Relative Stereochemical Assignment of (±)‐Gracilamine
inferred← citeshttps://doi.org/10.1002/ange.201405418openalex-snapshot
Total Synthesis of Gracilamine
inferred← citeshttps://doi.org/10.1002/ange.201409503openalex-snapshot
Total Syntheses of (−)‐Huperzine Q and (+)‐Lycopladines B and C
inferred← citeshttps://doi.org/10.1002/ange.201509602openalex-snapshot
Expedient Synthesis of (+)‐Lycopalhine A
inferred← citeshttps://doi.org/10.1002/ange.201700433openalex-snapshot
Enantioselective Iridium‐Catalyzed Allylic Substitution with 2‐Methylpyridines
inferred← citeshttps://doi.org/10.1002/anie.201103550openalex-snapshot
Asymmetric Total Synthesis of a Pentacyclic Lycopodium Alkaloid: Huperzine‐Q
inferred← citeshttps://doi.org/10.1002/anie.201106753openalex-snapshot
Total Syntheses of Lycopodium Alkaloids (+)‐Fawcettimine, (+)‐Fawcettidine, and (−)‐8‐Deoxyserratinine
inferred← citeshttps://doi.org/10.1002/anie.201205711openalex-snapshot
Potentially Biomimetic Total Synthesis and Relative Stereochemical Assignment of (±)‐Gracilamine
inferred← citeshttps://doi.org/10.1002/anie.201405418openalex-snapshot
Total Synthesis of Gracilamine
inferred← citeshttps://doi.org/10.1002/anie.201409503openalex-snapshot
Total Syntheses of (−)‐Huperzine Q and (+)‐Lycopladines B and C
inferred← citeshttps://doi.org/10.1002/anie.201509602openalex-snapshot
Expedient Synthesis of (+)‐Lycopalhine A
inferred← citeshttps://doi.org/10.1002/anie.201700433openalex-snapshot
Enantioselective Iridium‐Catalyzed Allylic Substitution with 2‐Methylpyridines
inferred← citeshttps://doi.org/10.1002/aoc.4210openalex-snapshot
Current Applications of Suzuki–Miyaura Coupling Reaction in The Total Synthesis of Natural Products: An update
inferred← citeshttps://doi.org/10.1002/asia.201101029openalex-snapshot
Formal Synthesis of (−)‐Cephalotaxine Based on a Tandem Hydroamination/Semipinacol Rearrangement Reaction
inferred← citeshttps://doi.org/10.1002/asia.201402614openalex-snapshot
Total Syntheses of Lycoposerramine‐V and 5‐epi‐Lycoposerramine‐V
inferred← citeshttps://doi.org/10.1002/asia.201700364openalex-snapshot
Divergent Total Syntheses of (−)‐Huperzine Q, (+)‐Lycopladine B, (+)‐Lycopladine C, and (−)‐4‐epi‐Lycopladine D
inferred← citeshttps://doi.org/10.1002/chem.201301715openalex-snapshot
Synthetic and DFT Studies Towards a Unified Approach to Phlegmarine Alkaloids: Aza‐Michael Intramolecular Processes Leading to 5‐Oxodecahydroquinolines
inferred← citeshttps://doi.org/10.1002/chem.201403163openalex-snapshot
Redox Divergent Synthesis of Fawcettimine‐Type Lycopodium Alkaloids
inferred← citeshttps://doi.org/10.1002/chem.202003741openalex-snapshot
The Total Synthesis of Diquinane‐Containing Natural Products
inferred← citeshttps://doi.org/10.1002/ece3.9617openalex-snapshot
Early land plants: Plentiful but neglected nutritional resources for herbivores?
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Fawcettimine‐Type Lycopodium Alkaloids as a Driving Force for Discoveries in Organic Synthesis
inferred← citeshttps://doi.org/10.1007/s11101-014-9384-yopenalex-snapshot
Huperzine A from Huperzia serrata: a review of its sources, chemistry, pharmacology and toxicology
inferred← citeshttps://doi.org/10.1007/s13659-012-0084-2openalex-snapshot
One-step synthesis of Lycopodium alkaloid (-)-huperzine W via Suzuki-Miyaura coupling
inferred← citeshttps://doi.org/10.1007/s13659-014-0030-6openalex-snapshot
Carinatines A and B, Lycopodium Alkaloids from Phlegmariurus carinatus
inferred← citeshttps://doi.org/10.1007/s13659-016-0111-9openalex-snapshot
Lyconadins G and H, Two Rare Lyconadin-Type Lycopodium Alkaloids from Lycopodium complanatum
inferred← citeshttps://doi.org/10.1007/s13659-017-0140-zopenalex-snapshot
Lycodine-Type Lycopodium Alkaloids from the Whole Plants of Huperzia serrata
inferred← citeshttps://doi.org/10.1016/b978-0-12-407774-4.00001-7openalex-snapshot
Lycopodium Alkaloids – Synthetic Highlights and Recent Developments
inferred← citeshttps://doi.org/10.1016/bs.aihch.2015.04.002openalex-snapshot
The Literature of Heterocyclic Chemistry, Part XIII, 2012–2013
inferred← citeshttps://doi.org/10.1016/bs.alkal.2014.12.001openalex-snapshot
Simple Indolizidine and Quinolizidine Alkaloids
inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.04.019openalex-snapshot
Serralongamines B–D, three new Lycopodium alkaloids from Lycopodium serratum var. longipetiolatum, and their inhibitory effects on foam cell formation in macrophages
inferred← citeshttps://doi.org/10.1016/j.cbi.2015.07.008openalex-snapshot
Kinetics and molecular docking studies of cholinesterase inhibitors derived from water layer of Lycopodiella cernua (L.) Pic. Serm. (II)
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Five new fawcettimine-related alkaloids from Lycopodium japonicum Thunb
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104181openalex-snapshot
Serratene triterpenoids and their biological activities from Lycopodiaceae plants
inferred← citeshttps://doi.org/10.1016/j.phymed.2014.12.007openalex-snapshot
Dendritic cells matured in the presence of the lycopodium alkaloid annotine direct T cell responses toward a Th2/Treg phenotype
inferred← citeshttps://doi.org/10.1016/j.phytochem.2016.12.022openalex-snapshot
Identification and characterization of L-lysine decarboxylase from Huperzia serrata and its role in the metabolic pathway of lycopodium alkaloid
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.09.001openalex-snapshot
Three Lycopodium alkaloids from Thai club mosses
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113250openalex-snapshot
Naming of new natural products: Standard, pitfalls and tips-and-tricks
inferred← citeshttps://doi.org/10.1016/j.phytol.2018.11.010openalex-snapshot
Phlenumdines D and E, new Lycopodium alkaloids from Phlegmariurus nummulariifolius, and their regulatory effects on macrophage differentiation during tumor development
inferred← citeshttps://doi.org/10.1016/j.tet.2011.05.107openalex-snapshot
Ten new fawcettimine-related alkaloids from three species of Lycopodium
inferred← citeshttps://doi.org/10.1016/j.tet.2013.05.028openalex-snapshot
Nine new lycopodine-type alkaloids from Lycopodium japonicum Thunb.
inferred← citeshttps://doi.org/10.1016/j.tet.2016.06.043openalex-snapshot
Synthesis of quinolizidine-containing lycopodium alkaloids and related natural products
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.03.097openalex-snapshot
Asymmetric total synthesis of Lycopodium alkaloid (+)-lycopladine A
inferred← citeshttps://doi.org/10.1016/s1875-5364(24)60579-0openalex-snapshot
Carbonic anhydrase-like enzymes in the formation of Lycopodium alkaloid
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00627openalex-snapshot
Identification of Lycopodium Alkaloids Produced by an Ultraviolet-Irradiated Strain of Paraboeremia, an Endophytic Fungus from Lycopodium serratum var. longipetiolatum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00754openalex-snapshot
Lycopodium Alkaloids: Lycoplatyrine A, an Unusual Lycodine–Piperidine Adduct from Lycopodium platyrhizoma and the Absolute Configurations of Lycoplanine D and Lycogladine H
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01660openalex-snapshot
Total Synthesis of Sieboldine A
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02723openalex-snapshot
Enantioselective Total Synthesis of Lycoposerramine-Z Using Chiral Phosphoric Acid Catalyzed Intramolecular Michael Addition
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00608openalex-snapshot
Formal Synthesis of Gracilamine Using Rh(I)-Catalyzed [3 + 2 + 1] Cycloaddition of 1-Yne–Vinylcyclopropanes and CO
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00900openalex-snapshot
Unified Synthesis of 10-Oxygenated Lycopodium Alkaloids: Impact of C10-Stereochemistry on Reactivity
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01719openalex-snapshot
Toward a Synthesis of Fawcettimine-Type Lycopodium Alkaloids: Stereocontrolled Synthesis of a Functionalized Azaspirocycle Precursor
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00961openalex-snapshot
Total Synthesis of Fawcettimine-Type Alkaloid, Lycojaponicumin A
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03339openalex-snapshot
Deciphering the Biosynthetic Mechanism of Pelletierine in Lycopodium Alkaloid Biosynthesis
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02737openalex-snapshot
Enantioselective Total Synthesis of (+)-Sieboldine A and Analogues Thereof
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00338openalex-snapshot
Total Synthesis of Lycopalhine A
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02065openalex-snapshot
Phleghenrines A–D and Neophleghenrine A, Bioactive and Structurally Rigid Lycopodium Alkaloids from Phlegmariurus henryi
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02072openalex-snapshot
Protecting-Group-Free Total Synthesis of (−)-Lycopodine via Phosphoric Acid Promoted Alkyne Aza-Prins Cyclization
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02322openalex-snapshot
Asymmetric Total Synthesis of (−)-Lycospidine A
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01633openalex-snapshot
Total Synthesis of Huperzine Q
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03555openalex-snapshot
Total Synthesis of Huperzine R
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00152openalex-snapshot
Hupercumines A and B, Lycopodium Alkaloids from Huperzia cunninghamioides, Inhibiting Acetylcholinesterase
inferred← citeshttps://doi.org/10.1021/jacs.7b03280openalex-snapshot
Total Synthesis of (±)-Lycojaponicumin D and Lycodoline-Type Lycopodium Alkaloids
inferred← citeshttps://doi.org/10.1021/jo301545yopenalex-snapshot
Total Syntheses of (+)-Alopecuridine, (+)-Sieboldine A, and (−)-Lycojapodine A
inferred← citeshttps://doi.org/10.1021/jo3017555openalex-snapshot
Collective Synthesis of Lycopodium Alkaloids and Tautomer Locking Strategy for the Total Synthesis of (−)-Lycojapodine A
inferred← citeshttps://doi.org/10.1021/jo400324topenalex-snapshot
Enantioselective Approach to Quinolizidines: Total Synthesis of Cermizine D and Formal Syntheses of Senepodine G and Cermizine C
inferred← citeshttps://doi.org/10.1021/ol3007138openalex-snapshot
Tandem Oxidative Dearomatization/Intramolecular Diels–Alder Reaction for Construction of the Tricyclic Core of Palhinine A
inferred← citeshttps://doi.org/10.1021/ol301534ropenalex-snapshot
Toward the Total Synthesis of Palhinine A: Expedient Assembly of Multifunctionalized Isotwistane Ring System with Contiguous Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1021/ol302701yopenalex-snapshot
Lycojaponicumins D and E: Two New Alkaloids from Lycopodium japonicum
inferred← citeshttps://doi.org/10.1021/ol303272wopenalex-snapshot
Toward a Unified Approach for the Lycopodines: Synthesis of 10-Hydroxylycopodine, Deacetylpaniculine, and Paniculine
inferred← citeshttps://doi.org/10.1021/ol400628hopenalex-snapshot
Syntheses of (±)-Serratine, (±)-Lycoposerramine T, and (±)-Lycopoclavamine B
inferred← citeshttps://doi.org/10.1021/ol401411mopenalex-snapshot
Isopalhinine A, a Unique Pentacyclic Lycopodium Alkaloid from Palhinhaea cernua
inferred← citeshttps://doi.org/10.1021/ol500978kopenalex-snapshot
Isolation and Complete Structural Assignment of Lycopodium Alkaloid Cernupalhine A: Theoretical Prediction and Total Synthesis Validation
inferred← citeshttps://doi.org/10.1021/ol502679vopenalex-snapshot
Collective Total Synthesis of Tetracyclic DiquinaneLycopodiumAlkaloids (+)-Paniculatine, (−)-Magellanine, (+)-Magellaninone and Analogues Thereof
inferred← citeshttps://doi.org/10.1021/ol503571aopenalex-snapshot
Synthesis of the Tetracyclic Skeleton of the Lycopodium Alkaloid Lycopladine H via a Pivotal Double Hydroformylation/Intramolecular Reductive Amination Sequence
inferred← citeshttps://doi.org/10.1038/s41586-023-06716-yopenalex-snapshot
Plant carbonic anhydrase-like enzymes in neuroactive alkaloid biosynthesis
inferred← citeshttps://doi.org/10.1039/c2cc35032gopenalex-snapshot
In situ formation of β-glycosyl imidinium triflate from participating thioglycosyl donors: elaboration to disarmed–armed iterative glycosylation
inferred← citeshttps://doi.org/10.1039/c5sc03262hopenalex-snapshot
Concise synthesis of (+)-fastigiatine
inferred← citeshttps://doi.org/10.1039/c7cc06367aopenalex-snapshot
Effect of protic additives in Cu-catalysed asymmetric Diels–Alder cycloadditions of doubly activated dienophiles: towards the synthesis of magellanine-type Lycopodium alkaloids
inferred← citeshttps://doi.org/10.1039/c7qo00262aopenalex-snapshot
Stereoselective strategies for the construction of polysubstituted piperidinic compounds and their applications in natural products’ synthesis
inferred← citeshttps://doi.org/10.1039/c8cc07799aopenalex-snapshot
Recent advances in the total synthesis of gracilamine
inferred← citeshttps://doi.org/10.1039/d0ob02399jopenalex-snapshot
Synthesis of an isomer of lycoplanine A via cascade cyclization to construct the spiro-N,O-acetal moiety
inferred← citeshttps://doi.org/10.1039/d1qo00087jopenalex-snapshot
Construction of the tetracyclic core of the Lycopodium alkaloid annotinolide C
inferred← citeshttps://doi.org/10.1039/d1ra08163bopenalex-snapshot
Samarium( ii ) iodide-mediated reactions applied to natural product total synthesis
inferred← citeshttps://doi.org/10.1055/s-0040-1705953openalex-snapshot
Synthesis of Cyclohexane-Angularly-Fused Triquinanes
inferred← citeshttps://doi.org/10.1101/2022.11.01.514683openalex-snapshot
Neofunctionalized carbonic anhydrases in the biosynthesis of neuroactive plant alkaloids
inferred← citeshttps://doi.org/10.1186/s12864-017-3615-8openalex-snapshot
Global transcriptome analysis of Huperzia serrata and identification of critical genes involved in the biosynthesis of huperzine A
inferred← citeshttps://doi.org/10.1248/cpb.c16-00171openalex-snapshot
New Lycopodine-Type Alkaloids from Lycopodium carinatum
inferred← citeshttps://doi.org/10.1248/cpb.c19-00872openalex-snapshot
Total Syntheses of Lycopodium and Monoterpenoid Indole Alkaloids Based on Biosynthesis-Inspired Strategies
inferred← citeshttps://doi.org/10.15625/2615-9023/v40n4.10848openalex-snapshot
Evaluation of the genetic diversity of Huperzia serrate by rapd markers
inferred← citeshttps://doi.org/10.17989/encsr973msropenalex-snapshot
ENCSR973MSR
inferred← citeshttps://doi.org/10.18006/2022.10(1).64.72openalex-snapshot
Differentiation Effect of Two Alkaloid Fractions from Vietnamese Lycopodiaceae on Mouse Neural Stem Cells
inferred← citeshttps://doi.org/10.32657/10356/72446openalex-snapshot
Studies towards the synthesis of bioactive natural products and development of new synthetic methods
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.73.1072openalex-snapshot
Recent Progress in Total Synthesis of Lycopodium Alkaloids
inferred← citeshttps://doi.org/10.53023/p.rasayan-20210526openalex-snapshot
Lycopodium Alkaloids from Thai Club Mosses
inferred← citeshttps://doi.org/10.70675/df877f77z5ffaz4bfcz9e52z3bb0e678aba9openalex-snapshot
Studies towards the synthesis of bioactive natural products and development of new synthetic methods
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