scholarly article | Q13442814 |
P356 | DOI | 10.1002/ANIE.201409104 |
P698 | PubMed publication ID | 25404258 |
P50 | author | Koji Hirano | Q43283445 |
Tetsuya Satoh | Q51063869 | ||
P2093 | author name string | Masahiro Miura | |
Ryosuke Sakae | |||
P2860 | cites work | Electrophilic amination of carbanions | Q29396247 |
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Copper-catalyzed intermolecular regioselective hydroamination of styrenes with polymethylhydrosiloxane and hydroxylamines | Q34371348 | ||
A simple, modular synthesis of substituted pyridines | Q37148230 | ||
Direct stereospecific amination of alkyl and aryl pinacol boronates | Q42401891 | ||
Efficient boron-copper additions to aryl-substituted alkenes promoted by NHC-based catalysts. enantioselective Cu-catalyzed hydroboration reactions | Q43153955 | ||
Copper(I)-catalyzed asymmetric monoborylation of 1,3-dienes: synthesis of enantioenriched cyclic homoallyl- and allylboronates. | Q43197804 | ||
Copper-catalyzed borylation of α-alkoxy allenes with bis(pinacolato)diboron: efficient synthesis of 2-boryl 1,3-butadienes | Q43826323 | ||
Cross [2 + 2] cycloaddition of bicyclic alkenes with alkynes mediated by cobalt complexes: a facile synthesis of cyclobutene derivatives | Q43827648 | ||
Et3B-induced radical addition of N,N-dichlorosulfonamide to alkenes and pyrrolidine formation via radical annulation | Q44399332 | ||
C-H activation/borylation/oxidation: a one-pot unified route to meta-substituted phenols bearing ortho-/para-directing groups | Q44488743 | ||
Scope of palladium-catalyzed alkylative ring opening | Q44753462 | ||
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Umpolung amination: nickel-catalyzed coupling reactions of N,N-dialkyl-N-chloroamines with diorganozinc reagents | Q46119450 | ||
Regioselective and stereospecific copper-catalyzed aminoboration of styrenes with bis(pinacolato)diboron and O-benzoyl-N,N-dialkylhydroxylamines. | Q46316712 | ||
Intermolecular, catalytic asymmetric hydroamination of bicyclic alkenes and dienes in high yield and enantioselectivity | Q46420791 | ||
Efficient homogeneous catalysis in the reduction of CO2 to CO. | Q46838850 | ||
Boron-masking strategy for the selective synthesis of oligoarenes via iterative Suzuki-Miyaura coupling. | Q51081567 | ||
Arylboration of alkenes by cooperative palladium/copper catalysis. | Q53555943 | ||
A masked diboron in Cu-catalysed borylation reaction: highly regioselective formal hydroboration of alkynes for synthesis of branched alkenylborons. | Q53575592 | ||
Copper-catalyzed enantioselective formal hydroamination of oxa- and azabicyclic alkenes with hydrosilanes and hydroxylamines. | Q53616988 | ||
Highly stereoselective synthesis of (borylmethyl)cyclopropylamines by copper-catalyzed aminoboration of methylenecyclopropanes. | Q53627331 | ||
Alcohol elimination chemistry of tetrakis(tert-butoxocopper) | Q57365498 | ||
Cuprous tert-butoxide. New and useful metalation reagent | Q57533329 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | stereoselectivity | Q903429 |
P304 | page(s) | 613-617 | |
P577 | publication date | 2014-11-17 | |
P1433 | published in | Angewandte Chemie International Edition | Q62023953 |
P1476 | title | Copper-catalyzed stereoselective aminoboration of bicyclic alkenes. | |
P478 | volume | 54 |
Q88918259 | A Modified System for the Synthesis of Enantioenriched N-Arylamines through Copper-Catalyzed Hydroamination |
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Q27300830 | An Umpolung Strategy for the Synthesis of β-Aminoketones via Copper-Catalyzed Electrophilic Amination of Cyclopropanols. |
Q92930331 | B(MIDA)-Containing Diborons |
Q98159727 | Beyond Carbon: Enantioselective and Enantiospecific Reactions with Catalytically Generated Boryl- and Silylcopper Intermediates |
Q36664169 | Copper Hydride Catalyzed Hydroamination of Alkenes and Alkynes |
Q50124413 | Enantioselective Synthesis of Trisubstituted Allenyl-B(pin) Compounds by Phosphine-Cu-Catalyzed 1,3-Enyne Hydroboration. Insights Regarding Stereochemical Integrity of Cu-Allenyl Intermediates |
Q64077239 | Unsymmetrical Diboron Reagents: Application in Borylation Reactions of Unsaturated Bonds |
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