IF5 affects the final stage of the Cl-F exchange fluorination in the synthesis of pentafluoro-λ6-sulfanyl-pyridines, pyrimidines and benzenes with electron-withdrawing substituents.

about

Silver-induced self-immolative Cl-F exchange fluorination of arylsulfur chlorotetrafluorides: synthesis of arylsulfur pentafluorides.An eccentric rod-like linear connection of two heterocycles: synthesis of pyridine trans-tetrafluoro-λ6-sulfanyl triazoles.

P2860

Q48629344-3F7A42E7-458F-4F9D-A375-FCC2C1B68A47 Q55399917-A0C54229-AA00-4105-8F85-DAA0915D79CB

P2860

IF5 affects the final stage of the Cl-F exchange fluorination in the synthesis of pentafluoro-λ6-sulfanyl-pyridines, pyrimidines and benzenes with electron-withdrawing substituents.

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http://www.wikidata.org/entity/Q52770217

description

2017 nî lūn-bûn

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2017年の論文

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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

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2017年學術文章

@yue

2017年學術文章

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name

IF5 affects the final stage of ...... tron-withdrawing substituents.

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IF5 affects the final stage of ...... tron-withdrawing substituents.

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type

Item

label

IF5 affects the final stage of ...... tron-withdrawing substituents.

@en

IF5 affects the final stage of ...... tron-withdrawing substituents.

@nl

prefLabel

IF5 affects the final stage of ...... tron-withdrawing substituents.

@en

IF5 affects the final stage of ...... tron-withdrawing substituents.

@nl

P1476

IF5 affects the final stage of ...... tron-withdrawing substituents.

@en

P2093

Benqiang Cui

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

Etsuko Tokunaga

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

Kohei Matsuzaki

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

Mikhail Kosobokov

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

P2860

The Halogen Bond

Halogen bonding: a paradigm in supramolecular chemistry

The synthesis and biological activity of pentafluorosulfanyl analogs of fluoxetine, fenfluramine, and norfenfluramine.

Polyfluorinated groups in medicinal chemistry.

Evaluation of tert-butyl isosteres: case studies of physicochemical and pharmacokinetic properties, efficacies, and activities.

Synthesis of Phthalocyanines with a Pentafluorosulfanyl Substituent at Peripheral Positions.

Discovery of practical production processes for arylsulfur pentafluorides and their higher homologues, bis- and tris(sulfur pentafluorides): Beginning of a new era of "super-trifluoromethyl" arene chemistry and its industry.

A specific and direct comparison of the trifluoromethyl and pentafluoro sulfanyl groups on the selective dopamine D(3) antagonist 3-(3-{[4-methyl-5-(4-methyl-1,3-oxazol-5-yl)-4H-1,2,4-triazol-3-yl]thio}propyl)-1-phenyl-3-azabicyclo[3.1.0]hexane temp

How to Twist, Split and Warp a σ-Hole with Hypervalent Halogens.

Formation of α-SF5-Enolate Enables Preparation of 3-SF5-Quinolin-2-ones, 3-SF5-Quinolines, and 3-SF5-Pyridin-2-ones: Evaluation of their Physicochemical Properties.

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5997-6000

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scholarly article

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10.1039/C7CC02802D

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English

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

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

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Norio Shibata

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2017-05-17T00:00:00Z

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28513647

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IF5 affects the final stage of the Cl-F exchange fluorination in the synthesis of pentafluoro-λ6-sulfanyl-pyridines, pyrimidines and benzenes with electron-withdrawing substituents.

about

P2860

P2860

IF5 affects the final stage of the Cl-F exchange fluorination in the synthesis of pentafluoro-λ6-sulfanyl-pyridines, pyrimidines and benzenes with electron-withdrawing substituents.

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