Synthesis and Reactivity of Fluoroalkyl Copper Complexes by the Oxycupration of Tetrafluoroethylene.

about

Fluorinated Vinylsilanes from the Copper-Catalyzed Defluorosilylation of Fluoroalkene Feedstocks.Practical tetrafluoroethylene fragment installation through a coupling reaction of (1,1,2,2-tetrafluorobut-3-en-1-yl)zinc bromide with various electrophiles

P2860

Q46262802-EFBB2BBB-91A7-45ED-9137-59D530582EDD Q58750258-6AD49FFE-7264-47A1-810F-B7C497B4B8B0

P2860

Synthesis and Reactivity of Fluoroalkyl Copper Complexes by the Oxycupration of Tetrafluoroethylene.

Item

http://www.wikidata.org/entity/Q48322781

description

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

Synthesis and Reactivity of Fl ...... ration of Tetrafluoroethylene.

@en

Synthesis and Reactivity of Fl ...... ration of Tetrafluoroethylene.

@nl

type

Item

label

Synthesis and Reactivity of Fl ...... ration of Tetrafluoroethylene.

@en

Synthesis and Reactivity of Fl ...... ration of Tetrafluoroethylene.

@nl

prefLabel

Synthesis and Reactivity of Fl ...... ration of Tetrafluoroethylene.

@en

Synthesis and Reactivity of Fl ...... ration of Tetrafluoroethylene.

@nl

P1476

Synthesis and Reactivity of Fl ...... ration of Tetrafluoroethylene.

@en

P2093

Masato Ohashi

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

Naoyoshi Ishida

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

Takuya Adachi

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

P2860

Late-Stage Fluorination: From Fundamentals to Application

Direct cupration of fluoroform.

Enantioselective copper-catalyzed carboetherification of unactivated alkenes.

Copper(I) phenoxide complexes in the etherification of aryl halides.

Copper-catalyzed intramolecular alkene carboetherification: synthesis of fused-ring and bridged-ring tetrahydrofurans.

Fluorine in pharmaceutical industry: fluorine-containing drugs introduced to the market in the last decade (2001-2011).

Synthesis and laboratory evaluation of 1-(2,6-disubstituted benzoyl)-3-phenylureas, a new class of insecticides. I. 1-(2,6-Dichlorobenzoyl)-3-phenylureas.

Copper-mediated perfluoroalkylation of heteroaryl bromides with (phen)CuRF.

Synthetic Approaches to Trifluoromethoxy-Substituted Compounds.

A broadly applicable copper reagent for trifluoromethylations and perfluoroalkylations of aryl iodides and bromides

P304

11911-11915

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

P31

scholarly article

P356

10.1002/ANIE.201703923

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

P407

English

P433

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

P478

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

P50

Kotaro Kikushima

Sensuke Ogoshi

P577

2017-06-06T00:00:00Z

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

P698

28585741

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

Synthesis and Reactivity of Fluoroalkyl Copper Complexes by the Oxycupration of Tetrafluoroethylene.

about

P2860

P2860

Synthesis and Reactivity of Fluoroalkyl Copper Complexes by the Oxycupration of Tetrafluoroethylene.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698