Chemoselective Alkene Hydrosilylation Catalyzed by Nickel Pincer Complexes. - Wikidata - awgldk - TriplyDB

Chemoselective Alkene Hydrosilylation Catalyzed by Nickel Pincer Complexes.

Chemoselective Alkene Hydrosilylation Catalyzed by Nickel Pincer Complexes.

http://www.wikidata.org/entity/Q51700280

about

Control of Selectivity through Synergy between Catalysts, Silanes and Reaction Conditions in Cobalt-Catalyzed Hydrosilylation of Dienes and Terminal Alkenes Silicon-Carbon Bond Formation via Nickel-Catalyzed Cross-Coupling of Silicon Nucleophiles with Unactivated Secondary and Tertiary Alkyl Electrophiles Selective Cobalt-Catalyzed Reduction of Terminal Alkenes and Alkynes Using (EtO)2Si(Me)H as a Stoichiometric Reductant.Asymmetric Copper Hydride-Catalyzed Markovnikov Hydrosilylation of Vinylarenes and Vinyl Heterocycles.Selective hydrosilylation of alkynes and ketones: contrasting reactivity between cationic 3-iminophosphine palladium and nickel complexes.Iron-Catalyzed Intermolecular 1,2-Difunctionalization of Styrenes and Conjugated Alkenes with Silanes and Nucleophiles.Dichotomy of Manganese Catalysis via Organometallic or Radical Mechanism: Stereodivergent Hydrosilylation of Alkynes.Pt nanoparticles immobilized in mesostructured silica: a non-leaching catalyst for 1-octene hydrosilylation.(Aminomethyl)pyridine Complexes for the Cobalt-Catalyzed Anti-Markovnikov Hydrosilylation of Alkoxy- or Siloxy(vinyl)silanes with Alkoxy- or Siloxyhydrosilanes.Ligands with 1,10-phenanthroline scaffold for highly regioselective iron-catalyzed alkene hydrosilylation.The Nickel-Pincer Complex in Lactate Racemase Is an Electron Relay and Sink that acts through Proton-Coupled Electron Transfer.Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction.Enantioselective NiH/Pmrox-Catalyzed 1,2-Reduction of α,β-Unsaturated Ketones.Stereoselective synthesis of vinylsilanes via copper-catalyzed silylation of alkenes with silanes.Conversion of alkanes to linear alkylsilanes using an iridium-iron-catalysed tandem dehydrogenation-isomerization-hydrosilylation.An Easily Accessed Nickel Nanoparticle Catalyst for Alkene Hydrosilylation with Tertiary Silanes.Walking Metals for Remote Functionalization.Regioselective hydrosilylation of epoxides catalysed by nickel(ii) hydrido complexes.Development of Nickel Hydrosilylation Catalysts.Olefin hydrosilylation catalyzed by cationic nickel(ii) allyl complexes: a non-innocent allyl ligand-assisted mechanism.Silylation reactions on nanoporous gold via homolytic Si–H activation of silanes† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8sc01427b.Dichotomy of Manganese Catalysis via Organometallic or Radical Mechanism: Stereodivergent Hydrosilylation of Alkynes Asymmetric remote C-H borylation of internal alkenes via alkene isomerization

P2860

Q33764249-458A2FC3-ABFD-4B6D-82CE-6C55AAC83C46 Q37272984-D5A7D3E5-11ED-45D2-9560-CBA573B2723B Q37574389-1F260968-BA60-497D-99A8-10EF5BC3E1B7 Q37745000-7209F65A-2D4E-4A56-A8DA-C3B490B3FCEA Q47892804-C4EC169A-3935-4E09-8DFE-B2FE023160B0 Q48165406-06FEFC84-F23E-4170-8596-A1E0414320E2 Q48178419-FB4C160A-689E-4803-B244-1123E4D422D8 Q48205416-A5D79E62-2836-46A4-81F9-3A31F644635F Q48224008-CD77ED79-F277-444D-9A63-A2AF6D9843F1 Q48239673-DAB69B79-9399-492D-A4E9-338605732BAD Q48280110-D6DCA415-AC9D-4C07-9035-FACA3A03FACF Q48344038-7356EBAE-4B51-43F3-AE28-EC2D23591D8D Q48350849-F88FC24E-8618-4656-8A35-641D6D6FC0AA Q49122781-4DB40B87-2D52-4977-A330-9C43A2E66746 Q50889393-A1AF5DDA-00F3-439B-A0CE-7980AE1FC8F7 Q51168232-9A5736EC-9C15-4CF2-8426-395B64B4E025 Q52358082-F1A35339-0C57-471B-9004-1FB042EFF57D Q52778697-E5C1FCF3-8764-47E6-BD84-EC4144366923 Q52843593-0B65BE73-C951-4CAB-AED5-583A4E6C6BF7 Q52872782-7E61405C-89CE-4AE3-BC00-F0552C1D5296 Q55080094-73F204B8-2F20-4904-BE33-B38204F2D94C Q57998090-EFB1E55D-7F92-4E29-A1F9-DDCF8503B76B Q58695780-CB2F7B31-DAD1-4780-9859-DC3A672354B7

P2860

Chemoselective Alkene Hydrosilylation Catalyzed by Nickel Pincer Complexes.

http://www.wikidata.org/entity/Q51700280

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh-hant

name

Chemoselective Alkene Hydrosilylation Catalyzed by Nickel Pincer Complexes.

@en

Chemoselective Alkene Hydrosilylation Catalyzed by Nickel Pincer Complexes.

@nl

type

label

Chemoselective Alkene Hydrosilylation Catalyzed by Nickel Pincer Complexes.

@en

Chemoselective Alkene Hydrosilylation Catalyzed by Nickel Pincer Complexes.

@nl

prefLabel

Chemoselective Alkene Hydrosilylation Catalyzed by Nickel Pincer Complexes.

@en

Chemoselective Alkene Hydrosilylation Catalyzed by Nickel Pincer Complexes.

@nl

P1433

Q51700280-BCCC7429-BB0B-4C71-845A-892C7D7D5341

P1476

Q51700280-F97127BF-A35E-4175-8A17-8A332A3C663D

P2093

Q51700280-3563C8A4-C149-44CE-8276-CD936D37AFD5

Q51700280-3F1BEB97-23A4-4447-B58E-325E6D2C91E9

Q51700280-9F756F5C-321B-437F-95CD-A520D330005C

Q51700280-BEE9B929-43DE-4B7D-B14E-29181D7522D8

P2860

Q51700280-0B9F5374-AA5B-456F-9EB1-79396327210D

Q51700280-0C244D55-1FCE-48AF-A690-21F0055A23F4

Q51700280-1F24DA0F-A8ED-4384-950E-E46B361B0D42

Q51700280-35609C80-727D-4F60-801C-E32424A67B70

Q51700280-39301213-7FB4-459D-B162-68E07BEC5057

Q51700280-4E734298-A48F-4810-B2D0-AEC26D61E855

Q51700280-533F3812-0D76-45CD-AF4B-575318033242

Q51700280-5E937A84-D9E5-43F6-959F-39FC2950D018

Q51700280-638A94F4-90E5-4D5A-90EC-8FAEC4D2BEE0

Q51700280-69745452-D22A-4A66-8E28-F4BA8813F6B0

P304

Q51700280-323043E1-A41F-4A2E-BB27-EC86B5CEBEDE

P31

Q51700280-DB7E541A-9DC8-4B2D-BD26-4DA94E9D6769

P356

Q51700280-BBD79496-C90F-42DA-8339-B0E8FC192762

P407

Q51700280-599DB897-AEA8-468E-9FF5-D536DA97D83F

P433

Q51700280-28966E18-9C67-492F-A593-4C4EB3043D86

P478

Q51700280-6DA72993-1AA1-46C2-80D5-49A10A8AB65A

P50

Q51700280-9298926E-634E-4A50-A351-90B303001A16

P577

Q51700280-03EA1B71-B314-4A39-81BC-5DB70E86B298

P698

Q51700280-A6222CF5-9D27-4804-8F47-964971C4A1D2

P921

Q51700280-5115808a-d027-4b58-9688-78b4868a1d6a

P356

P1433

Angewandte Chemie International Edition

P1476

Chemoselective Alkene Hydrosilylation Catalyzed by Nickel Pincer Complexes.

@en

P2093

Ivan Buslov

http://www.w3.org/2001/XMLSchema#string

Jeanne Becouse

http://www.w3.org/2001/XMLSchema#string

Mickael Montandon-Clerc

http://www.w3.org/2001/XMLSchema#string

Simona Mazza

http://www.w3.org/2001/XMLSchema#string

P2860

The Addition of Silicon Hydrides to Olefinic Double Bonds. Part II. The Use of Group VIII Metal Catalysts

Recent advances and actual challenges in late transition metal catalyzed hydrosilylation of olefins from an industrial point of view

Iron catalysts for selective anti-Markovnikov alkene hydrosilylation using tertiary silanes.

General and practical one-pot synthesis of dihydrobenzosiloles from styrenes.

Ni-catalyzed Sonogashira coupling of nonactivated alkyl halides: orthogonal functionalization of alkyl iodides, bromides, and chlorides.

Preparation and molecular and electronic structures of iron(0) dinitrogen and silane complexes and their application to catalytic hydrogenation and hydrosilation.

Functional group tolerant Kumada-Corriu-Tamao coupling of nonactivated alkyl halides with aryl and heteroaryl nucleophiles: catalysis by a nickel pincer complex permits the coupling of functionalized Grignard reagents.

Synthesis and reactivity of a conveniently prepared two-coordinate bis(amido) nickel(II) complex.

Bis(imino)pyridine cobalt-catalyzed alkene isomerization-hydroboration: a strategy for remote hydrofunctionalization with terminal selectivity.

Phosphinite-iminopyridine iron catalysts for chemoselective alkene hydrosilylation.

P304

14523-14526

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/ANIE.201507829

http://www.w3.org/2001/XMLSchema#string

P407

P433

48

http://www.w3.org/2001/XMLSchema#string

P478

54

http://www.w3.org/2001/XMLSchema#string

P50

P577

2015-10-02T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

26428272

http://www.w3.org/2001/XMLSchema#string

P921