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Pictet–Spengler reactions in multiphasic supercritical carbon dioxide/CO2-expanded liquid media. In situ generation of carbamates as a strategy for reactions of amines in supercritical carbon dioxide

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

inferredcites →https://doi.org/10.1002/1521-3765(20011105)7:21<4584::aid-chem4584>3.0.co;2-popenalex-snapshot
Supercritical Carbon Dioxide as Solvent and Temporary Protecting Group for Rhodium-Catalyzed Hydroaminomethylation
inferredcites →https://doi.org/10.1007/3-540-48664-x_5openalex-snapshot
Reactions in Supercritical Carbon Dioxide (scCO2)
inferredcites →https://doi.org/10.1016/j.tet.2004.05.065openalex-snapshot
Lithium heptadecafluorooctanesulfonate catalyzed Mannich-type and aza-Diels–Alder reactions in supercritical carbon dioxide
inferredcites →https://doi.org/10.1016/s0040-4020(01)80894-2openalex-snapshot
Mechanistic studies on the role of carbon dioxide in the synthesis of methylcarbamates from amines and dimethylcarbonate in the Presence of CO2.
inferredcites →https://doi.org/10.1016/s0040-4039(01)02390-5openalex-snapshot
The synthesis of alkyl carbamates from primary aliphatic amines and dialkyl carbonates in supercritical carbon dioxide
inferredcites →https://doi.org/10.1016/s0896-8446(02)00087-6openalex-snapshot
Fluid phase equilibria of the reacting mixture in the dimethyl carbonate synthesis from supercritical CO2
inferredcites →https://doi.org/10.1021/ac020527popenalex-snapshot
Reaction Monitoring of Aliphatic Amines in Supercritical Carbon Dioxide by Proton Nuclear Magnetic Resonance Spectroscopy and Implications for Supercritical Fluid Chromatography
inferredcites →https://doi.org/10.1021/ar010076fopenalex-snapshot
The Chemistry of Dimethyl Carbonate
inferredcites →https://doi.org/10.1021/cr00038a004openalex-snapshot
The Pictet-Spengler condensation: a new direction for an old reaction
inferredcites →https://doi.org/10.1021/cr0306182openalex-snapshot
Cyclizations of N -Acyliminium Ions
inferredcites →https://doi.org/10.1021/cr940266mopenalex-snapshot
Converting Carbon Dioxide into Carbamato Derivatives
inferredcites →https://doi.org/10.1021/ja010952kopenalex-snapshot
Olefin Metathesis in Supercritical Carbon Dioxide
inferredcites →https://doi.org/10.1021/ja953097bopenalex-snapshot
Homogeneous Catalysis in Supercritical Fluids: Hydrogenation of Supercritical Carbon Dioxide to Formic Acid, Alkyl Formates, and Formamides
inferredcites →https://doi.org/10.1021/ja984309iopenalex-snapshot
Iridium-Catalyzed Enantioselective Hydrogenation of Imines in Supercritical Carbon Dioxide
inferredcites →https://doi.org/10.1021/je034089aopenalex-snapshot
Vapor−Liquid Equilibria of Binary Carbon Dioxide + Alkyl Carbonate Mixture Systems
inferredcites →https://doi.org/10.1021/jo0477796openalex-snapshot
Synthesis of Methyl Carbamates from Primary Aliphatic Amines and Dimethyl Carbonate in Supercritical CO2: Effects of Pressure and Cosolvents and Chemoselectivity
inferredcites →https://doi.org/10.1021/jo9704523openalex-snapshot
Concerning the Regiochemical Course of the Diels−Alder Reaction in Supercritical Carbon Dioxide
inferredcites →https://doi.org/10.1021/jp960180sopenalex-snapshot
Kinetic Correlation of Diels−Alder Reactions in Supercritical Carbon Dioxide
inferredcites →https://doi.org/10.1021/jp984227gopenalex-snapshot
Silica-Promoted Diels−Alder Reactions in Carbon Dioxide from Gaseous to Supercritical Conditions
inferredcites →https://doi.org/10.1039/a908819iopenalex-snapshot
Catalytic production of urethanes from amines and alkyl halides in supercritical carbon dioxide
inferredcites →https://doi.org/10.1039/b101219nopenalex-snapshot
The use of supercritical fluids in synthetic organic chemistry
inferredcites →https://doi.org/10.1039/b404564popenalex-snapshot
Organic synthesis using enzymes in supercritical carbon dioxide
inferredcites →https://doi.org/10.1039/b406868hopenalex-snapshot
Palladium catalysed cross-coupling reactions of silylamines
inferredcites →https://doi.org/10.1039/b411561aopenalex-snapshot
Nitrile oxide cycloadditions in supercritical carbon dioxide
inferredcites →https://doi.org/10.2174/1385272053369330openalex-snapshot
Selective Catalytic Oxidations in Supercritical Carbon Dioxide

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4521724openalex-extracted
Supercritical Carbon Dioxide Fluid-Assisted Green Production and Dyeing of N,4-Dialkyl-Substituted 1,8-Naphthalimide Derivatives
inferred← citeshttps://doi.org/10.1002/9781118686263.ch10openalex-snapshot
Tetrahydroisoquinolines
inferred← citeshttps://doi.org/10.1002/9783527628698.hgc037openalex-snapshot
Expanded Liquid Phases in Catalysis: Gas‐expanded Liquids and Liquid–Supercritical Fluid Biphasic Systems
inferred← citeshttps://doi.org/10.1002/ange.201008071openalex-snapshot
Die Pictet‐Spengler‐Reaktion in der Natur und der organischen Chemie
inferred← citeshttps://doi.org/10.1002/anie.201008071openalex-snapshot
The Pictet–Spengler Reaction in Nature and in Organic Chemistry
inferred← citeshttps://doi.org/10.1002/chin.200602146openalex-snapshot
Pictet—Spengler Reactions in Multiphasic Supercritical Carbon Dioxide/CO2‐Expanded Liquid Media. In situ Generation of Carbamates as a Strategy for Reactions of Amines in Supercritical Carbon Dioxide.
inferred← citeshttps://doi.org/10.1002/ejoc.201600313openalex-snapshot
First Synthesis of (R)‐ and (S)‐1,2,3,4‐Tetrahydroisoquinoline‐3‐phosphonic Acid (TicP) Using a Pictet–Spengler Reaction
inferred← citeshttps://doi.org/10.1002/slct.201900524openalex-snapshot
Synthesis of Functionalised Indoline and Isoquinoline Derivatives through a Silylcarbocyclisation/Desilylation Sequence
inferred← citeshttps://doi.org/10.1007/978-1-4939-2493-6_1002-1openalex-snapshot
Replacement of Toxic Feedstocks in Chemical Synthesis
inferred← citeshttps://doi.org/10.1007/978-1-4939-9060-3_1002openalex-snapshot
Replacement of Toxic Feedstocks in Chemical Synthesis
inferred← citeshttps://doi.org/10.1007/s11426-010-0073-4openalex-snapshot
Pictet-Spengler condensation reactions catalyzed by a recyclable H+-montmorillonite as a heterogeneous Brønsted acid
inferred← citeshttps://doi.org/10.1007/s11426-010-4026-8openalex-snapshot
Co(acac)3/BMMImCl as a base-free catalyst system for clean syntheses of N,N′-disubstituted ureas from amines and CO2
inferred← citeshttps://doi.org/10.1016/j.supflu.2005.12.011openalex-snapshot
Catalytic chain transfer polymerisation of CO2-expanded methyl methacrylate
inferred← citeshttps://doi.org/10.1016/j.supflu.2007.11.014openalex-snapshot
Novel CO2-soluble pyridine derivatives and the extraction of heavy metals into Sc-CO2
inferred← citeshttps://doi.org/10.1016/j.supflu.2023.106085openalex-snapshot
Supercritical carbon dioxide fluid-assisted green production and dyeing of N,4-dialkyl-substituted 1,8-naphthalimide derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2007.02.123openalex-snapshot
Synthesis of tetrahydroisoquinolines and isochromans via Pictet–Spengler reactions catalyzed by Brønsted acid–surfactant-combined catalyst in aqueous media
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.11.147openalex-snapshot
Pictet–Spengler reactions catalyzed by Brønsted acid-surfactant-combined catalyst in water or aqueous media
inferred← citeshttps://doi.org/10.1016/s0959-6380(07)80016-xopenalex-snapshot
Six-membered ring systems: pyridines and benzo derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00710openalex-snapshot
The Formation of Seven-Membered Heterocycles under Mild Pictet–Spengler Conditions: A Route to Pyrazolo[3,4]benzodiazepines
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00928openalex-snapshot
Transition-Metal-Free Oxidative Cross-Coupling of Triorganoindium Reagents with Tetrahydroisoquinolines
inferred← citeshttps://doi.org/10.1021/acs.langmuir.7b02881openalex-snapshot
Novelty of Dynamic Process in the Synthesis of Biocompatible Silica Nanotubes by Biomimetic Glycyldodecylamide as a Soft Template
inferred← citeshttps://doi.org/10.1021/cr040199oopenalex-snapshot
Gas-Expanded Liquids
inferred← citeshttps://doi.org/10.1021/cr068435dopenalex-snapshot
Alternative Synthetic Methods through New Developments in Catalysis by Gold
inferred← citeshttps://doi.org/10.1021/ie071453gopenalex-snapshot
Influence of Compressed Carbon Dioxide on Hydrogenation Reactions in Cyclohexane with a Pd/C Catalyst
inferred← citeshttps://doi.org/10.1021/je900948nopenalex-snapshot
Vapor−Liquid Equilibrium Data and Predictive Correlations for the Carbon Dioxide−Dimethyl Carbonate Binary Mixture
inferred← citeshttps://doi.org/10.1021/jo0619783openalex-snapshot
Acid-Promoted Cyclization Reactions of Tetrahydroindolinones. Model Studies for Possible Application in a Synthesis of Selaginoidine
inferred← citeshttps://doi.org/10.1021/jo9021875openalex-snapshot
Synthesis of Amides and Lactams in Supercritical Carbon Dioxide
inferred← citeshttps://doi.org/10.1039/b904097hopenalex-snapshot
A critical look at reactions in class I and II gas-expanded liquids using CO2 and other gases
inferred← citeshttps://doi.org/10.1039/c4ob01446dopenalex-snapshot
Diversity-oriented synthesis of medicinally important 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) derivatives and higher analogs
inferred← citeshttps://doi.org/10.1039/d0qo00722fopenalex-snapshot
Pictet–Spengler reaction based on in situ generated α-amino iminium ions through the Heyns rearrangement
inferred← citeshttps://doi.org/10.1055/sos-sd-115-00651openalex-snapshot
15.5.4 Isoquinolines (Update 2019)
inferred← citeshttps://doi.org/10.1070/rcr4628openalex-snapshot
The progress in the chemistry of N-acyliminium ions and their use in stereoselective organic synthesis
inferred← citeshttps://doi.org/10.1080/00304940609356447openalex-snapshot
THE PICTET-SPENGLER REACTION: EFFICIENT CARBON-CARBON BOND FORMING REACTION IN HETEROCYCLIC SYNTHESIS
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Ag-mediated synthesis of six-membered N-heterocycles
inferred← citeshttps://doi.org/10.1515/psr-2021-0027openalex-snapshot
Bronsted acidic surfactants: efficient organocatalysts for diverse organic transformations
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Direct and Efficient C(sp3)–H Functionalization of N-Acyl/Sulfonyl Tetrahydroisoquinolines (THIQs) With Electron-Rich Nucleophiles via 2,3-Dichloro-5,6-Dicyano-1,4-Benzoquinone (DDQ) Oxidation
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