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Palladium-catalyzed coupling of tetraorganotin compounds with aryl and benzyl halides. Synthetic utility and mechanism

https://doi.org/10.1021/ja00511a032
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Total synthesis studies on macrocyclic pipecolic acid natural products: FK506, the antascomicins and rapamycin
inferred← citeshttps://doi.org/10.1007/978-981-10-3193-9_8openalex-snapshot
Palladium-Catalyzed Decarboxylative Benzylation of α-Cyano Aliphatic Carboxylate Salts with Benzyl Electrophiles
inferred← citeshttps://doi.org/10.1007/978-981-92-0108-2_10openalex-snapshot
Synthesis and Electronic Properties of π-Conjugated Polymers
inferred← citeshttps://doi.org/10.1007/bf00954359openalex-snapshot
Coupling reaction of organomercury compounds with aryl halides catalyzed by palladium complexes
inferred← citeshttps://doi.org/10.1007/bf01557731openalex-snapshot
Organometallic compounds in synthesis and catalysis
inferred← citeshttps://doi.org/10.1007/s00214-015-1726-3openalex-snapshot
Dissecting the bond-formation process of d 10-metal–ethene complexes with multireference approaches
inferred← citeshttps://doi.org/10.1007/s00706-012-0746-0openalex-snapshot
Recent advances in application of intramolecular Suzuki cross-coupling in cyclization and heterocyclization
inferred← citeshttps://doi.org/10.1007/s00706-012-0838-xopenalex-snapshot
Recent advances in Kumada-Tamao-Corriu cross-coupling reaction catalyzed by different ligands
inferred← citeshttps://doi.org/10.1007/s00706-019-2364-6openalex-snapshot
Advances in Kumada–Tamao–Corriu cross-coupling reaction: an update
inferred← citeshttps://doi.org/10.1007/s00706-023-03148-2openalex-snapshot
Recent advances on palladium incorporated clay-based heterogeneous catalyst for carbon–carbon coupling reactions
inferred← citeshttps://doi.org/10.1007/s00894-015-2802-2openalex-snapshot
DFT studies on the palladium-catalyzed dearomatization reaction between naphthalene allyl chloride and allyltributylstannane
inferred← citeshttps://doi.org/10.1007/s10562-015-1614-4openalex-snapshot
Pd- and Ni-Pyridyl Complexes Deposited as Films for Suzuki–Miyaura and Mizoroki–Heck Cross Coupling Reactions
inferred← citeshttps://doi.org/10.1016/0020-1693(95)04799-9openalex-snapshot
Synthesis and characterisation of a heterodinuclear ruthenium(II)palladium(II) complex with two different cyclometallating sites
inferred← citeshttps://doi.org/10.1016/0022-328x(83)85077-3openalex-snapshot
The cross-coupling reactions of organic halides with organic derivatives of tin, mercury and copper catalyzed by palladium
inferred← citeshttps://doi.org/10.1016/0022-328x(85)80208-4openalex-snapshot
Palladium- and nickel-catalyzed aryl- and acyl-demetallation of organometallic compounds
inferred← citeshttps://doi.org/10.1016/0022-328x(85)87365-4openalex-snapshot
Regio- and stereo-selective synthesis of vinylstannanes. Transition-metal catalyzed stannylmetalation of acetylenes and conversion of enol triflates and vinyl iodides into vinylstannanes
inferred← citeshttps://doi.org/10.1016/0022-328x(87)80020-7openalex-snapshot
Synthèse et thermolyse éclair d'esters α-tributylstanniques
inferred← citeshttps://doi.org/10.1016/0022-328x(87)80048-7openalex-snapshot
Palladium-catalyzed or -promoted reductive carbon-carbon coupling. Effects of phosphines and carbon ligands
inferred← citeshttps://doi.org/10.1016/0022-328x(88)87019-0openalex-snapshot
Palladium-(II) and -(IV) complexes as intermediates in catalytic CC bond-forming reactions
inferred← citeshttps://doi.org/10.1016/0022-328x(89)87037-8openalex-snapshot
Palladium-catalyzed acyldemetallation and carbonylation reactions of organomercurials for the synthesis of unsymmetrical ketones
inferred← citeshttps://doi.org/10.1016/0022-328x(89)87065-2openalex-snapshot
Studies of oxidative addition-reductive elimination reactions, and the crystal structure of the palladium(IV) complex Me2(p-BrC6H4CH2)Pd(phen)Br
inferred← citeshttps://doi.org/10.1016/0022-328x(91)86321-gopenalex-snapshot
Changing selectivity in palladiu-catalyzed reactioins involving oxidation state IV. A new synthesis from iodobenzene and norbornene
inferred← citeshttps://doi.org/10.1016/0022-328x(93)80486-uopenalex-snapshot
Regioselective ring opening of a palladium(IV) alkylaromatic metallacycle by benzyl group migration from palladium to the aromatic carbon and X-ray structure of the resulting palladium(II) complex
inferred← citeshttps://doi.org/10.1016/0040-4020(89)80004-3openalex-snapshot
Et3B induced radical addition of Ph3SnH to acetylenes and its application to cyclization reaction
inferred← citeshttps://doi.org/10.1016/0040-4020(89)80010-9openalex-snapshot
Palladium catalyzed coupling of organostannanes with vinyl epoxides
inferred← citeshttps://doi.org/10.1016/0304-5102(90)85256-hopenalex-snapshot
Syntheses of new chiral ferrocenylamine sulfide and selenide complexes of group X metals and their application to enantioselective cross-coupling reactions and selective hydrogenation
inferred← citeshttps://doi.org/10.1016/0304-5102(93)80018-popenalex-snapshot
Palladium-catalyzed carbon—carbon bond formation from (η6-chloroarene)Cr(CO)3 complexes an example of bimetallic activation in homogeneous catalysis
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00022-2openalex-snapshot
Ions, Radicals, Carbenes, and Other Monocoordinated Systems
inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/00233-8openalex-snapshot
Ions, Radicals, Carbenes and Other Monocoordinated Systems
inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/00237-5openalex-snapshot
One or More CC Bond(s) Formed by Substitution or Addition
inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/09009-9openalex-snapshot
References to Volume 1
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00103-5openalex-snapshot
Palladium–Carbon σ-Bonded Complexes
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00013-5openalex-snapshot
Nucleophilic Addition to Carboxylic Acid Derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00069-xopenalex-snapshot
Coupling Reactions Between sp3 and sp2 Carbon Centers
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00070-6openalex-snapshot
Coupling Reactions Between sp2 Carbon Centers
inferred← citeshttps://doi.org/10.1016/b978-0-08-092493-9.50010-4openalex-snapshot
Asymmetric Coupling Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-08-096701-1.00243-3openalex-snapshot
Coupling Reactions in Polymer Synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00312-8openalex-snapshot
3.08 Coupling Reactions Between sp3 and sp2 Carbon Centers
inferred← citeshttps://doi.org/10.1016/b978-0-12-811292-2.00002-7openalex-snapshot
Stille Cross-Coupling Reaction: Early Years to the Current State of the Art
inferred← citeshttps://doi.org/10.1016/b978-0-12-811292-2.00005-2openalex-snapshot
Application of Heck Alkenylation Reaction in Modified Nucleoside Synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00070-3openalex-snapshot
Coupling Reactions Between sp3 and sp2 Carbon Centers
inferred← citeshttps://doi.org/10.1016/b978-0-408-01435-9.50016-xopenalex-snapshot
Access to carbon–carbon bonds
inferred← citeshttps://doi.org/10.1016/b978-0-443-16166-7.00021-9openalex-snapshot
Green metal catalyzed reactions under sustainable conditions toward medicinally potent biomolecules
inferred← citeshttps://doi.org/10.1016/b978-0-89232-948-9.50007-1openalex-snapshot
Transition Metal Catalyzed Silylmetalation of Acetylenes and ET3B-Induced Radical Addition of PH3SNH to Acetylenes
inferred← citeshttps://doi.org/10.1016/b978-008044412-3/50005-1openalex-snapshot
Cross-coupling reactions of arylmetallic reagents with aryl halides and sulfonates
inferred← citeshttps://doi.org/10.1016/b978-008046519-7.00080-0openalex-snapshot
Palladium Carbon σ-Bonded Complexes
inferred← citeshttps://doi.org/10.1016/b978-008046519-7.00111-8openalex-snapshot
Transition Metal Alkyl Complexes: Oxidative Addition and Transmetallation
inferred← citeshttps://doi.org/10.1016/b978-044453138-4/50010-6openalex-snapshot
The chemistry of PCP pincer phosphinite transition metal complexes
inferred← citeshttps://doi.org/10.1016/bs.apoc.2023.08.001openalex-snapshot
Nickel and palladium catalysed cross-coupling: Factors effecting the oxidative addition step
inferred← citeshttps://doi.org/10.1016/j.apcata.2011.09.014openalex-snapshot
Heck reactions catalyzed by Pd(0)-PVP nanoparticles under conventional and microwave heating
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.06.098openalex-snapshot
Synthesis and biological evaluation of tetracyclic fluoroquinolones as antibacterial and anticancer agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.03.018openalex-snapshot
Synthesis and biological evaluation of tetracyclic thienopyridones as antibacterial and antitumor agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.05.025openalex-snapshot
Discovery of novel prostaglandin analogs of PGE2 as potent and selective EP2 and EP4 receptor agonists
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.05.009openalex-snapshot
The role of CuI in the siloxane-mediated Pd-catalyzed cross-coupling reactions of aryl iodides with aryl lithium reagents
inferred← citeshttps://doi.org/10.1016/j.ccr.2011.11.007openalex-snapshot
Secondary phosphine oxides: Versatile ligands in transition metal-catalyzed cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.ccr.2015.01.011openalex-snapshot
Microwave-assisted synthesis – Catalytic applications in aqueous media
inferred← citeshttps://doi.org/10.1016/j.ccr.2025.216431openalex-snapshot
Greener media for nano catalysts in Suzuki Miyaura reaction
inferred← citeshttps://doi.org/10.1016/j.heliyon.2026.e45172openalex-snapshot
From scope to strategy: Recent advances in Suzuki cross-coupling for efficient total synthesis and molecule editing
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