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Organic Superbases in Lewis Pair Catalyzed Hydrogenations of Imines

https://doi.org/10.2139/ssrn.6024727
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9780470740859openalex-snapshot
Superbases for Organic Synthesis
inferredcites →https://doi.org/10.1002/adsc.200404076openalex-snapshot
Functionalization of Alkynes Catalyzed by t‐Bu‐P4 Base
inferredcites →https://doi.org/10.1002/anie.202215899openalex-snapshot
Direct Deprotonative Functionalization of α,α‐Difluoromethyl Ketones using a Catalytic Organosuperbase
inferredcites →https://doi.org/10.1002/anie.202407822openalex-snapshot
Facile Access to Organostibines via Selective Organic Superbase Catalyzed Antimony‐Carbon Protonolysis
inferredcites →https://doi.org/10.1002/anie.202411249openalex-snapshot
An Expedient Route to Bio‐Based Polyacrylate Alternatives with Inherent Post‐Chemical Modification and Degradation Capabilities by Organic Catalysis for Polymerization of Muconate Esters
inferredcites →https://doi.org/10.1002/chem.201804370openalex-snapshot
“Inverse” Frustrated Lewis Pairs: An Inverse FLP Approach to the Catalytic Metal Free Hydrogenation of Ketones
inferredcites →https://doi.org/10.1002/chem.201900498openalex-snapshot
Phosphazene Base tBu‐P4 Catalyzed Methoxy–Alkoxy Exchange Reaction on (Hetero)Arenes
inferredcites →https://doi.org/10.1007/128_2012_392openalex-snapshot
Frustrated Lewis Pair Mediated Hydrogenations
inferredcites →https://doi.org/10.1016/j.jphotochem.2017.02.016openalex-snapshot
Remarkable difference between five- and six- number-membered ring transition states for intramolecular proton transfer in excited state
inferredcites →https://doi.org/10.1021/acs.accounts.1c00297openalex-snapshot
Design of Novel Uncharged Organic Superbases: Merging Basicity and Functionality
inferredcites →https://doi.org/10.1021/acs.accounts.7b00530openalex-snapshot
Frustrated Lewis Pairs Catalyzed Asymmetric Metal-Free Hydrogenations and Hydrosilylations
inferredcites →https://doi.org/10.1021/acs.inorgchem.4c03002openalex-snapshot
Investigation of Phosphazene Superbase Interactions with [PCl2N]3
inferredcites →https://doi.org/10.1021/acs.joc.6b00872openalex-snapshot
Experimental Basicities of Superbasic Phosphonium Ylides and Phosphazenes
inferredcites →https://doi.org/10.1021/acs.jpca.6b01552openalex-snapshot
Experimental Basicities of Phosphazene, Guanidinophosphazene, and Proton Sponge Superbases in the Gas Phase and Solution
inferredcites →https://doi.org/10.1021/acs.macromol.1c01514openalex-snapshot
Organocatalyzed Group Transfer Polymerization of Alkyl Sorbate: Polymer Synthesis, Postpolymerization Modification, and Thermal Properties
inferredcites →https://doi.org/10.1021/acs.organomet.0c00411openalex-snapshot
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes
inferredcites →https://doi.org/10.1021/acs.orglett.0c03507openalex-snapshot
Catalytic C(sp2)–C(sp3) Bond Formation of Methoxyarenes by the Organic Superbase t-Bu-P4
inferredcites →https://doi.org/10.1021/acs.orglett.2c03870openalex-snapshot
Phosphazene Base-Catalyzed Intramolecular Hydroamidation of Alkenes with Amides
inferredcites →https://doi.org/10.1021/acs.orglett.9b02309openalex-snapshot
Catalytic Amination of β-(Hetero)arylethyl Ethers by Phosphazene Base t-Bu-P4
inferredcites →https://doi.org/10.1021/acscatal.0c00753openalex-snapshot
Superbase-Catalyzed Stereo- and Regioselective Glycosylation with 2-Nitroglycals: Facile Access to 2-Amino-2-deoxy-O-glycosides
inferredcites →https://doi.org/10.1021/acscatal.1c01515openalex-snapshot
Unlocking the Catalytic Hydrogenolysis of Chlorosilanes into Hydrosilanes with Superbases
inferredcites →https://doi.org/10.1021/acscatal.2c03901openalex-snapshot
Organosuperbase-Catalyzed 1,1-Diboration of Alkynes
inferredcites →https://doi.org/10.1021/ic200663vopenalex-snapshot
Metal-Free Catalytic Hydrogenation of Polar Substrates by Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1021/ja067961jopenalex-snapshot
Facile Heterolytic Cleavage of Dihydrogen by Phosphines and Boranes
inferredcites →https://doi.org/10.1021/jacs.1c13397openalex-snapshot
Mechanistic Studies Yield Improved Protocols for Base-Catalyzed Anti-Markovnikov Alcohol Addition Reactions
inferredcites →https://doi.org/10.1021/jacs.4c09042openalex-snapshot
Catalytic Concerted S N Ar Reactions of Fluoroarenes by an Organic Superbase
inferredcites →https://doi.org/10.1021/jacs.5b13545openalex-snapshot
“Inverse” Frustrated Lewis Pairs – Activation of Dihydrogen with Organosuperbases and Moderate to Weak Lewis Acids
inferredcites →https://doi.org/10.1021/jacs.5c07849openalex-snapshot
Bifunctional Iminophosphorane Superbases Enable the Highly Enantioselective Sulfa-Michael Addition to Fully Substituted Cyclopropene Carboxylic Acid Derivatives
inferredcites →https://doi.org/10.1021/jacs.8b00766openalex-snapshot
Superbase-Catalyzed anti-Markovnikov Alcohol Addition Reactions to Aryl Alkenes
inferredcites →https://doi.org/10.1021/jo034537hopenalex-snapshot
Acid−Base Equilibria in Nonpolar Media. 4. Extension of the Self-Consistent Basicity Scale in THF Medium. Gas-Phase Basicities of Phosphazenes
inferredcites →https://doi.org/10.1021/jp012168sopenalex-snapshot
Intrinsic Basicities of Phosphorus Imines and Ylides: A Theoretical Study
inferredcites →https://doi.org/10.1021/jp066182mopenalex-snapshot
Experimental Gas-Phase Basicity Scale of Superbasic Phosphazenes
inferredcites →https://doi.org/10.1039/a800453fopenalex-snapshot
Superbase catalysis of oxazolidin-2-one ring formation from carbon dioxide and prop-2-yn-1-amines under homogeneous or heterogenous conditions
inferredcites →https://doi.org/10.1039/b508541aopenalex-snapshot
Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy
inferredcites →https://doi.org/10.1039/b700140aopenalex-snapshot
Nucleophilic aromatic substitution using Et3SiH/cat. t-Bu-P4 as a system for nucleophile activation
inferredcites →https://doi.org/10.1039/b710475hopenalex-snapshot
Rapid intramolecular heterolytic dihydrogen activation by a four-membered heterocyclic phosphane–borane adduct
inferredcites →https://doi.org/10.1039/b814812kopenalex-snapshot
Basicity of organic bases and superbases in acetonitrile by the polarized continuum model and DFT calculations
inferredcites →https://doi.org/10.1039/b913588jopenalex-snapshot
Phosphazene base-catalyzed intramolecular cyclization for efficient synthesis of benzofurans via carbon–carbon bond formation
inferredcites →https://doi.org/10.1039/c0cc03106bopenalex-snapshot
Metal-free deprotonative functionalization of heteroaromatics using organic superbase catalyst
inferredcites →https://doi.org/10.1039/c2dt30427aopenalex-snapshot
Lewis pair polymerization by classical and frustrated Lewis pairs: acid, base and monomer scope and polymerization mechanism
inferredcites →https://doi.org/10.1039/c2ob25339aopenalex-snapshot
“Frustrated Lewis pair” hydrogenations
inferredcites →https://doi.org/10.1039/c3cc46100aopenalex-snapshot
Phosphazene-catalyzed intramolecular cyclization of nitrogen-tethered alkynyl esters
inferredcites →https://doi.org/10.1039/c8cs00277kopenalex-snapshot
FLP catalysis: main group hydrogenations of organic unsaturated substrates
inferredcites →https://doi.org/10.1039/d2sc02827aopenalex-snapshot
A base-catalyzed approach for the anti-Markovnikov hydration of styrene derivatives
inferredcites →https://doi.org/10.1039/d3cc05878fopenalex-snapshot
Hexacoordinated tin complexes catalyse imine hydrogenation with H 2
inferredcites →https://doi.org/10.1039/d4cc05169fopenalex-snapshot
Phosphazene base-catalyzed telescopic three-component reaction involving 1,1-difunctionalization of electron-deficient alkenes
inferredcites →https://doi.org/10.1063/1.464913openalex-snapshot
Density-functional thermochemistry. III. The role of exact exchange
inferredcites →https://doi.org/10.1107/s0021889808042726openalex-snapshot
OLEX2 : a complete structure solution, refinement and analysis program
inferredcites →https://doi.org/10.3998/ark.5550190.0005.912openalex-snapshot
EtN=P(NMe2)N=P(NMe2)3: An efficient non-ionic base catalyst for the isomerization of allylic compounds and methylene-interrupted dienes
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