Tandem trifluoromethylthiolation/aryl migration of aryl alkynoates to trifluoromethylthiolated alkenes.

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Tandem trifluoromethylthiolation/aryl migration of aryl alkynoates to trifluoromethylthiolated alkenes.

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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-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

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2017年學術文章

@zh-hant

name

Tandem trifluoromethylthiolati ...... fluoromethylthiolated alkenes.

@en

Tandem trifluoromethylthiolati ...... fluoromethylthiolated alkenes.

@nl

type

Item

label

Tandem trifluoromethylthiolati ...... fluoromethylthiolated alkenes.

@en

Tandem trifluoromethylthiolati ...... fluoromethylthiolated alkenes.

@nl

prefLabel

Tandem trifluoromethylthiolati ...... fluoromethylthiolated alkenes.

@en

Tandem trifluoromethylthiolati ...... fluoromethylthiolated alkenes.

@nl

P1476

Tandem trifluoromethylthiolati ...... ifluoromethylthiolated alkenes

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P2093

Feng-Ling Qing

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

Huan Li

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

Shuai Liu

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Xiu-Hua Xu

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P2860

A survey of Hammett substituent constants and resonance and field parameters

Structural reevaluation of the electrophilic hypervalent iodine reagent for trifluoromethylthiolation supported by the crystalline sponge method for X-ray analysis

Alpha-fluorinated ethers, thioethers, and amines: anomerically biased species.

Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions.

Copper-promoted sulfenylation of sp2 C-H bonds.

Difluorocarbene-Derived Trifluoromethylthiolation and [(18)F]Trifluoromethylthiolation of Aliphatic Electrophiles

Oxidative trifluoromethylation and trifluoromethylthiolation reactions using (trifluoromethyl)trimethylsilane as a nucleophilic CF3 source.

Synthetic methods for compounds having CF3-S units on carbon by trifluoromethylation, trifluoromethylthiolation, triflylation, and related reactions.

Late stage trifluoromethylthiolation strategies for organic compounds.

Trifluoromethylthiolation of aryl iodides and bromides enabled by a bench-stable and easy-to-recover dinuclear palladium(i) catalyst.

P304

10136-10139

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P31

scholarly article

P356

10.1039/C7CC06232J

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P407

English

P433

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

P478

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

P50

Yangen Huang

P577

2017-09-01T00:00:00Z

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P698

28848946

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