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Total Synthesis of (+)-Condylocarpine, (+)-Isocondylocarpine, and (+)-Tubotaiwine

https://doi.org/10.1021/ol102709s
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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/hlca.19610440725openalex-snapshot
Alkaloide aus Diplorrhynchus condylocarpon (M UELL . A RG .) P ICHON ssp. mossambicensis (B ENTH .) D UVIGN
inferredcites →https://doi.org/10.1002/hlca.19630460616openalex-snapshot
Chemische Korrelation von Condylocarpin mit Akuammicin
inferredcites →https://doi.org/10.1002/hlca.19720550304openalex-snapshot
Über die Indolalkaloide von Pleiocarpa talbotii Wernham. 145. Mitteilung über Alkaloide
inferredcites →https://doi.org/10.1002/hlca.19720550830openalex-snapshot
Tubotaiwin‐N‐oxid aus der Wurzelrinde von Conopharyngia johnstoni Stapf. 148. Mitteilung über Alkaloide
inferredcites →https://doi.org/10.1002/jhet.5570390212openalex-snapshot
Synthesis of the azocino[4,3‐b]indole core structure for the synthesis of strychnos alkaloids
inferredcites →https://doi.org/10.1002/jhet.5570430310openalex-snapshot
A new approach to the total synthesis of (±)‐20‐ epidasycarpidone
inferredcites →https://doi.org/10.1007/978-3-7091-8888-0_2openalex-snapshot
The Condylocarpine Group of Indole Alkaloids
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/10.1016/0040-4020(81)85060-0openalex-snapshot
Syntheses in the ellipticine-olivacine series
inferredcites →https://doi.org/10.1016/0040-4039(95)00047-gopenalex-snapshot
Synthetic applications of 2-(1,3-Dithian-2-yl)indoles V.1 asymmetric synthesis of dasycarpidone-type indole alkaloids
inferredcites →https://doi.org/10.1016/s0040-4020(01)87370-1openalex-snapshot
Studies on the synthesis of indole alkaloids of condylocarpine type. C-4 alkylation of the 1-alkyl-3-(hydrazono)-2-piperidone system
inferredcites →https://doi.org/10.1016/s0040-4020(01)88234-xopenalex-snapshot
Studies on the nucleophilic addition to 3,5-disubstituted pyridinium salts
inferredcites →https://doi.org/10.1016/s0040-4020(01)88607-5openalex-snapshot
2-Cyano Δ3 piperideines—IX
inferredcites →https://doi.org/10.1016/s0040-4039(00)95539-4openalex-snapshot
An enantioselective access to the (−)-tubotaiwine skeleton
inferredcites →https://doi.org/10.1021/ja00352a038openalex-snapshot
Pentacyclic systems of indole alkaloids. Formation of the C11-C12 bond. Two syntheses of (.+-.)-aspidospermidine
inferredcites →https://doi.org/10.1021/ja00411a058openalex-snapshot
Dimethylmethylthiosulfonium fluoroborate. A chemoselective initiator for thionium ion induced cyclizations
inferredcites →https://doi.org/10.1021/ja00739a022openalex-snapshot
Stereospecific syntheses of uleine and epiuleine
inferredcites →https://doi.org/10.1021/ja01096a055openalex-snapshot
Dimethyl Sulfoxide-Acid Anhydride Mixtures. New Reagents for Oxidation of Alcohols1
inferredcites →https://doi.org/10.1021/ja0399021openalex-snapshot
Enantioselective Synthesis of (−)-Gilbertine via a Cationic Cascade Cyclization
inferredcites →https://doi.org/10.1021/ja100178uopenalex-snapshot
Total Synthesis of (±)- and (−)-Actinophyllic Acid
inferredcites →https://doi.org/10.1021/ja803158yopenalex-snapshot
Total Synthesis of (±)-Actinophyllic Acid
inferredcites →https://doi.org/10.1021/jo00008a024openalex-snapshot
Total syntheses of tubotaiwine and 19,20-dihydro-20-epi-akuammicine
inferredcites →https://doi.org/10.1021/jo00027a016openalex-snapshot
Studies on the synthesis of Strychnos alkaloids. A new entry into the azocino[4,3-b]indole core structure and related studies
inferredcites →https://doi.org/10.1021/jo00047a047openalex-snapshot
Studies on the synthesis of pentacyclic Strychnos indole alkaloids. Closure of the E ring by Pummerer cyclization
inferredcites →https://doi.org/10.1021/jo00093a028openalex-snapshot
Total Synthesis of Uleine-Type and Strychnos Alkaloids through a Common Intermediate
inferredcites →https://doi.org/10.1021/jo00111a053openalex-snapshot
Syntheses of Strychnos- and Aspidospermatan-Type Alkaloids. 7. Total Syntheses of Lagunamine, Isolagunamine, Condylocarpine, and Isocondylocarpine
inferredcites →https://doi.org/10.1021/jo00313a017openalex-snapshot
A new synthetic entry to pentacyclic Strychnos alkaloids. Total synthesis of (.+-.)-tubifolidine, (.+-.)-tubifoline, and (.+-.)-19,20-dihydroakuammicine
inferredcites →https://doi.org/10.1021/jo801998hopenalex-snapshot
A New Acyl Radical-based Route to the 1,5-Methanoazocino[4,3-b]indole Framework of Uleine and Strychnos Alkaloids
inferredcites →https://doi.org/10.1021/jo962169uopenalex-snapshot
Palladium(0)-Catalyzed Heteroarylation of 2- and 3-Indolylzinc Derivatives. An Efficient General Method for the Preparation of (2-Pyridyl)indoles and Their Application to Indole Alkaloid Synthesis
inferredcites →https://doi.org/10.1039/a700856bopenalex-snapshot
First enantiocontrolled syntheses of (+)-uleine and (+)-dasycarpidone
inferredcites →https://doi.org/10.1039/c2969000665bopenalex-snapshot
Total synthesis of (±)-tubotaiwine (dihydrocondylocarpine)
inferredcites →https://doi.org/10.1039/c39910000614openalex-snapshot
Total synthesis of the Strychnos alkaloid tubotaiwine
inferredcites →https://doi.org/10.1039/j39690002738openalex-snapshot
The syntheses of (±)-dasycarpidone, (±)-3-epi-dasycarpidone, (±)-uleine and (±)-3-epi-uleine
inferredcites →https://doi.org/10.1055/s-1995-3950openalex-snapshot
Domino Reactions - New Concepts in the Synthesis of Indole Alkaloids and Other Polycyclic Indole Derivatives
inferredcites →https://doi.org/10.1139/v83-426openalex-snapshot
Enamines of 2,2-bis(ethylthio)ethanal: a convenient route to γ-keto crotonate derivatives
inferredcites →https://doi.org/10.1351/pac197541010167openalex-snapshot
Synthetic studies in the strychnos-type alkaloid field
inferredcites →https://doi.org/10.3987/com-05-s(k)12openalex-snapshot
Studies on the Preparation of 1,5-Methanoazocinoindole Based on Indolylborate

What points at this work

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

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New Synthesis of Β-Aryl-Gaba Drugs
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Protection for the Amino Group
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Rhodium‐Catalyzed C−H Functionalization of Indoles with Diazo Compounds: Synthesis of Structurally Diverse 2,3‐Fused Indoles
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A Synthesis of Novel Tetracyclic Azocino[4,3‐b]Indole Framework: Combined Spectroscopic, DFT, Molecular Docking, and ADMET Analysis
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Indole Synthesis via Allenyl Ester; Enantioselective Total Synthesis of Geissoschizoline
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Structure Determination and Total Synthesis of (+)‐16‐Hydroxy‐16,22‐dihydroapparicine
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Synthetic Studies on the Initially Proposed Structure of Protoaculeine B: Discovery of Neuronally Active Heterotricyclic Amino Acids
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Synthesis and stereochemical determination of an antiparasitic pseudo-aminal type monoterpene indole alkaloid
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Structural, electronic, and spectroscopic study on 1,5-methanoazocino[4,3-b]indole synthesized by TFB-based route
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Monoterpene indole alkaloids from Vinca minor L. (Apocynaceae): Identification of new structural scaffold for treatment of Alzheimer's disease
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Concise total synthesis of (±)-actinophyllic acid
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Advances in dearomatization strategies of indoles
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New synthesis of β-aryl-GABA drugs
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The first total synthesis and reassignment of the relative stereochemistry of 16-hydroxy-16,22-dihydroapparicine
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Halogen-Bonding-Promoted C–H Malonylation of Indoles under Visible-Light Irradiation
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02717openalex-snapshot
Synthesis of Trifluoroacetamidoketones by Acylation of Ferrocene with In Situ Protected Amino Acids
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Palladium-Catalyzed Ullmann Cross-Coupling/Tandem Reductive Cyclization Route to Key Members of the Uleine Alkaloid Family
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General Approach toward Aspidospermatan-Type Alkaloids Using One-Pot Vilsmeier–Haack Cyclization and Azomethine Ylide Cycloaddition
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Rh-Catalyzed [3 + 2] Cycloaddition of 1-Sulfonyl-1,2,3-triazoles: Access to the Framework of Aspidosperma and Kopsia Indole Alkaloids
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Total Synthesis of (+)-epi-Condyfoline
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[RhCp*Cl 2 ] 2 -Catalyzed Indole Functionalization: Synthesis of Bioinspired Indole-Fused Polycycles
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Synthesis of (±)-Actinophyllic Acid and Analogs: Applications of Cascade Reactions and Diverted Total Synthesis
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A Raney-Cobalt-Mediated Tandem Reductive Cyclization Route to the 1,5-Methanoazocino[4,3-b]indole Framework of the Uleine and Strychnos Alkaloids
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Formal Synthesis of (±)-Cycloclavine
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Synthetic Study toward the Misassigned (±)-Tronoharine
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Synthesis of Structurally Diverse 2,3-Fused Indoles via Microwave-Assisted AgSbF6-Catalysed Intramolecular Difunctionalization of o-Alkynylanilines
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Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
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2-Methoxyphenyl isocyanate: a chemoselective multitasking reagent for an amine protection/deprotection sequence
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A de novo synthesis of the bisindole alkaloid geissolosimine: collective synthesis of geissoschizoline, akuammicine, (16 S )-deshydroxymethylstemmadenine and Aspidospermatan alkaloids
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Concise Total Synthesis of 20-Deethyl-4-demethyldasycarpidone
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A New Approach to the Total Synthesis of 20-Deethyltubifolidine and an Entry to the Azocino[4,3-b]indoles
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Missing enzymes in the biosynthesis of the anticancer drug vinblastine in Madagascar periwinkle
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Advances in the synthesis of cycloalka[b]indoles
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An Improved Approach to the Synthesis of Tetracyclic 20-Deethyl-4-demethyldasycarpidone and 20-Deethyldasycarpidone
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Désaromatisation radicalaire d'indoles pour la synthèse de spiroindolines trifluorométhylées ou phosphorées
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