The one-pot synthesis of quinolines via Co(iii)-catalyzed C-H activation/carbonylation/cyclization of anilines.

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The one-pot synthesis of quinolines via Co(iii)-catalyzed C-H activation/carbonylation/cyclization of anilines.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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The one-pot synthesis of quinolines via Co

@nl

The one-pot synthesis of quino ...... ation/cyclization of anilines.

@en

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Item

label

The one-pot synthesis of quinolines via Co

@nl

The one-pot synthesis of quino ...... ation/cyclization of anilines.

@en

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The one-pot synthesis of quinolines via Co

@nl

The one-pot synthesis of quino ...... ation/cyclization of anilines.

@en

P1476

The one-pot synthesis of quino ...... ation/cyclization of anilines.

@en

P2093

Wei Yi

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

Xin Chen

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

Xu Zhang

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

Xuefeng Xu

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Yurong Yang

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P2860

On the mechanism of the Skraup-Doebner-Von Miller quinoline synthesis

Cobalt(III)-catalyzed synthesis of indazoles and furans by C-H bond functionalization/addition/cyclization cascades.

Reversed reactivity of anilines with alkynes in the rhodium-catalysed C-H activation/carbonylation tandem

Recent advances in the synthesis of indole and quinoline derivatives through cascade reactions.

A mild and efficient one-step synthesis of quinolines.

Highly Stereoselective Cobalt(III)-Catalyzed Three-Component C-H Bond Addition Cascade

A cationic high-valent Cp*Co(III) complex for the catalytic generation of nucleophilic organometallic species: directed C-H bond activation.

Reductive carbonylation of aryl halides employing a two-chamber reactor: a protocol for the synthesis of aryl aldehydes including 13C- and D-isotope labeling.

Rh(I)-catalyzed CO gas-free cyclohydrocarbonylation of alkynes with formaldehyde to alpha,beta-butenolides.

Pyrroloindolone synthesis via a Cp*Co(III)-catalyzed redox-neutral directed C-H alkenylation/annulation sequence.

P304

9061-9065

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P31

scholarly article

P356

10.1039/C7OB02310C

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P433

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

P478

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

P577

2017-10-23T00:00:00Z

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P698

29058750

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