Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes.

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Catalytic Carbo- and Aminoboration of Alkenyl Carbonyl Compounds via 5- and 6-Membered Palladacycles.Transition Metal-Free 1,2-Carboboration of Unactivated Alkenes.

P2860

Q48135177-EB9BEBB0-2957-449D-BC7F-A20BF2EDE479 Q55288423-CE58BB8F-3168-461E-8166-92D4C6AB4590

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Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes.

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http://www.wikidata.org/entity/Q48357236

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes.

@en

Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes.

@nl

type

Item

label

Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes.

@en

Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes.

@nl

prefLabel

Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes.

@en

Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes.

@nl

P1476

Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes

@en

P2093

Kaitlyn M Logan

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

Sean D White

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

Stephen R Sardini

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

P2860

Recent advances in homogeneous nickel catalysis

Configurationally Stable, Enantioenriched Organometallic Nucleophiles in Stereospecific Pd-Catalyzed Cross-Coupling Reactions: An Alternative Approach to Asymmetric Synthesis

Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners

Enantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents To Construct C-C Bonds

Nickel-catalyzed coupling reactions of alkyl electrophiles, including unactivated tertiary halides, to generate carbon-boron bonds.

Practical carbon-carbon bond formation from olefins through nickel-catalyzed reductive olefin hydrocarbonation.

Catalytic Enantioselective Functionalization of Unactivated Terminal Alkenes

Asymmetric synthesis from terminal alkenes by cascades of diboration and cross-coupling

Transition-metal-catalyzed laboratory-scale carbon-carbon bond-forming reactions of ethylene

Stereospecific functionalizations and transformations of secondary and tertiary boronic esters.

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159-162

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

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scholarly article

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10.1021/JACS.7B12160

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

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English

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

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140

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

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M Kevin Brown

P577

2017-12-22T00:00:00Z

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

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29271650

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

P921

Iztāctepoztli

stereoselectivity

P932

5778876

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

Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes.

about

P2860

P2860

Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932