Reductive coupling of benzyl oxalates with highly functionalized alkyl bromides by nickel catalysis.

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Reductive coupling of benzyl oxalates with highly functionalized alkyl bromides by nickel catalysis.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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name

Reductive coupling of benzyl o ...... bromides by nickel catalysis.

@en

Reductive coupling of benzyl o ...... bromides by nickel catalysis.

@nl

type

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label

Reductive coupling of benzyl o ...... bromides by nickel catalysis.

@en

Reductive coupling of benzyl o ...... bromides by nickel catalysis.

@nl

prefLabel

Reductive coupling of benzyl o ...... bromides by nickel catalysis.

@en

Reductive coupling of benzyl o ...... bromides by nickel catalysis.

@nl

P1476

Reductive coupling of benzyl o ...... l bromides by nickel catalysis

@en

P2093

Chun-Ling Li

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

Peng Guo

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Wen-Jie Jin

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Xiao-Biao Yan

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P2860

Nickel-catalyzed asymmetric reductive cross-coupling between vinyl and benzyl electrophiles.

Dialkyl Ether Formation by Nickel-Catalyzed Cross-Coupling of Acetals and Aryl Iodides.

Nickel-catalyzed cross-couplings involving carbon-oxygen bonds

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

New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles.

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.

Selective cross-coupling of organic halides with allylic acetates.

Activation and functionalization of benzylic derivatives by palladium catalysts.

Stereospecific nickel-catalyzed cross-coupling reactions of alkyl Grignard reagents and identification of selective anti-breast-cancer agents.

P304

4529-4534

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P31

scholarly article

P356

10.1039/C8SC00609A

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P433

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

P478

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

P50

Xing-zhong Shu

P577

2018-04-20T00:00:00Z

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P698

29896396

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P932

5961445

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