About: Transition-Metal (Pd, Ni, Mn)-Catalyzed C-C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks

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About: Transition-Metal (Pd, Ni, Mn)-Catalyzed C-C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks Goto Sponge NotDistinct Permalink

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scientific article published on 25 March 2019

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rdf:type	Item
description	wetenschappelijk artikel (nl) artículu científicu espublizáu en marzu de 2019 (ast) scientific article published on 25 March 2019 (en) наукова стаття, опублікована 25 березня 2019 (uk)
publication date	wds:Q92595457-F71F6DB1-8B59-40D9-BB9E-D07BD48EBC10
publication date	2019-03-25 00:00:00Z (xsd:dateTime)
cites work	wds:Q92595457-088EF79B-CE9D-47CF-84E9-5EA1DA735680 wds:Q92595457-1B57DB2B-1D62-46A7-94D1-EBE94C5544BA wds:Q92595457-29A015E0-82E5-4D3D-A3B1-86131DEFBA38 wds:Q92595457-2F2872B1-BE93-4094-A14E-B0D0A6B0F60D wds:Q92595457-448D6D81-7551-4E65-8849-091F7F77A56C wds:Q92595457-4A272A8A-3A75-4B5E-81B7-F8FCAF91F3EA wds:Q92595457-5DBF03FD-DD3B-4469-9D4C-AEF2C32EB42C wds:Q92595457-6B59F2ED-8B93-4AC7-A37E-C9975840DB88 wds:Q92595457-723C50F9-A911-4338-A365-15EE822E19ED wds:Q92595457-728F8E64-4979-4DF2-8907-95E7DB0EF16C wds:Q92595457-785D6791-9448-4BA6-B9A5-BFCFCA8F8FF3 wds:Q92595457-7A6B57AD-588F-4F96-820F-6A3CDBC07006 wds:Q92595457-7B07C05E-58B0-4FF7-A582-5E1342DD2FD2 wds:Q92595457-7E735DF0-0E4E-49FB-A41A-E6D2D15810B9 wds:Q92595457-7F423852-F00E-431F-BD14-9EF0516582FA wds:Q92595457-84F98F62-D8BD-429E-AC5A-DDA385DAF5B5 wds:Q92595457-863B8E19-891C-4B18-A67A-506F91F52452 wds:Q92595457-884EA51E-801B-413F-B615-BA62951709F9 wds:Q92595457-92E5E435-A590-4D68-BA94-7D596686388E wds:Q92595457-95D5FD1F-2CA2-4F65-A776-C0002B248CAA wds:Q92595457-965EC785-DB3B-4465-91E6-97B81B574530 wds:Q92595457-9AD3DF39-03ED-4966-BC46-7361CDBDF023 wds:Q92595457-A7454117-7F08-4F16-A71F-FF970E81541F wds:Q92595457-B1C05843-47A3-4BE1-88E1-ABDD6520CDDC wds:Q92595457-B469523A-AC43-4E4E-9AD1-C3A5FA54CF70 wds:Q92595457-C05C05C1-02EC-4A24-9377-37EE0BCB74F1 wds:Q92595457-C2DD18C6-C244-432E-A998-C1CDDD3ADD00 wds:Q92595457-D4668228-CD99-4DF0-9DCC-280C7DE38F49 wds:Q92595457-DB40F642-B11B-49F3-B771-5178F13A2D7A wds:Q92595457-DD3A0C5E-5313-4742-9B6E-EB7223EE4045 wds:Q92595457-E654EE74-FAC2-4966-A3ED-37F13437714A wds:Q92595457-E91B2E29-86DC-49DC-833C-9D19E329380A wds:Q92595457-EA22F084-97EB-4202-BE41-C1178F8FA836 wds:Q92595457-F3E8BE2F-0CBF-4AE4-BFBB-B4F896F0FFB9 wds:Q92595457-F5557D4E-2016-4AD5-B9D5-1C6677135777
cites work	Catalysts for Cross-Coupling Reactions with Non-activated Alkyl Halides Recent advances in homogeneous nickel catalysis Pd-catalyzed cross-coupling reactions of alkyl halides Room-temperature alkyl-alkyl Suzuki cross-coupling of alkyl bromides that possess beta hydrogens Palladium-Catalyzed Cross-Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize Transition Metal-Catalyzed Activation of Aliphatic C−X Bonds in Carbon−Carbon Bond Formation Palladium-catalyzed carbonylation reactions of aryl halides and related compounds Boronic acids: new coupling partners in room-temperature Suzuki reactions of alkyl bromides. Crystallographic characterization of an oxidative-addition adduct generated under remarkably mild conditions Toward an improved understanding of the unusual reactivity of Pd0/trialkylphosphane catalysts in cross-couplings of alkyl electrophiles: quantifying the factors that determine the rate of oxidative addition. Intramolecular Heck reactions of unactivated alkyl halides Palladium-catalyzed Heck-type reactions of alkyl iodides Palladium-catalyzed carbonylative Heck-type reactions of alkyl iodides Palladium-catalyzed Heck-type cross-couplings of unactivated alkyl iodides Nickel-catalyzed Heck-type alkenylation of secondary and tertiary α-carbonyl alkyl bromides Auto-tandem catalysis: a single catalyst activating mechanistically distinct reactions in a single reactor. A review of new developments in the Friedel-Crafts alkylation - From green chemistry to asymmetric catalysis Manganese-Catalyzed Carboacylations of Alkenes with Alkyl Iodides. Synthesis using aromatic homolytic substitution--recent advances Mechanism of thermal decomposition of trans-diethylbis(tertiary phosphine)palladium(II). Steric effects of tertiary phosphine ligands on the stability of diethylpalladium complexes Radicals in transition metal catalyzed reactions? transition metal catalyzed radical reactions?: a fruitful interplay anyway: part 3: catalysis by group 10 and 11 elements and bimetallic catalysis Carbonylation reactions of alkyl iodides through the interplay of carbon radicals and Pd catalysts. Palladium-catalyzed, ring-forming aromatic C-H alkylations with unactivated alkyl halides Transition Metal-Catalyzed Dicarbofunctionalization of Unactivated Olefins. Palladium-Catalyzed Alkoxycarbonylation of Unactivated Secondary Alkyl Bromides at Low Pressure Cobalt-catalyzed trimethylsilylmethylmagnesium-promoted radical alkenylation of alkyl halides: a complement to the Heck reaction. Cobalt-catalyzed Heck-type reaction of alkyl halides with styrenes Palladium-Catalyzed Carbocyclizations of Unactivated Alkyl Bromides with Alkenes Involving Auto-tandem Catalysis. Nickel-Catalyzed Mizoroki-Heck-Type Reactions of Unactivated Alkyl Bromides Water control over the chemoselectivity of a Ti/Ni multimetallic system: Heck- or reductive-type cyclization reactions of alkyl iodides An efficient generation of a functionalized tertiary-alkyl radical for copper-catalyzed tertiary-alkylative Mizoroki-Heck type reaction Room-Temperature Hiyama Cross-Couplings of Arylsilanes with Alkyl Bromides and Iodides Atom-transfer cyclization. A novel isomerization of hex-5-ynyl iodides to iodomethylene cyclopentanes Cascade radical reactions catalyzed by a Pd/light system: cyclizative multiple carbonylation of 4-alkenyl iodides Effective acceleration of atom transfer carbonylation of alkyl iodides by metal complexes. Application to the synthesis of the hinokinin precursor and dihydrocapsaicin Nickel-catalysed novel β,γ-unsaturated nitrile synthesis
author name string	wds:Q92595457-40D2FB34-1D61-403A-8773-78BA4DA2EA11
author name string	Megan R Kwiatkowski
rdfs:label	Transition-Metal (Pd, Ni, Mn)-Catalyzed C-C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks (en) Transition-Metal (Pd, Ni, Mn)-Catalyzed C-C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks (nl)
skos:prefLabel	Transition-Metal (Pd, Ni, Mn)-Catalyzed C-C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks (en) Transition-Metal (Pd, Ni, Mn)-Catalyzed C-C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks (nl)
name	Transition-Metal (Pd, Ni, Mn)-Catalyzed C-C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks (en) Transition-Metal (Pd, Ni, Mn)-Catalyzed C-C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks (nl)
author	wds:Q92595457-12352C4B-13D4-4F96-A8D7-1EA789AFC2CE
author	Erik J Alexanian
title	wds:Q92595457-74CDD756-4EB6-4B01-ADCF-7792340AFE4D
title	Transition-Metal (Pd, Ni, Mn)-Catalyzed C-C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks (en)
page(s)	wds:Q92595457-A9F64B2C-2C8F-4FB9-AB8C-D96BF794BA5B
page(s)	1134-1144
instance of	wds:Q92595457-57C368A7-34DF-4CF4-8327-B4A78B7C58BD
instance of	scholarly article
PubMed ID	wds:Q92595457-8AEC1EC5-1CA9-4F2F-A1AB-0C29B3E3F738
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30908013
PubMed ID	30908013
published in	wds:Q92595457-EE5BA29D-DC3E-4641-BE9C-5F52C2AE1140
published in	Accounts of Chemical Research
issue	wds:Q92595457-9128298A-533A-421F-B2C9-2BB0D05F01B4
volume	wds:Q92595457-66AD55A8-FBC5-4B09-BACB-B49207AF4564

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