Arenium ions are not obligatory intermediates in electrophilic aromatic substitution. - Wikidata - awgldk - TriplyDB

Arenium ions are not obligatory intermediates in electrophilic aromatic substitution.

Arenium ions are not obligatory intermediates in electrophilic aromatic substitution.

http://www.wikidata.org/entity/Q33925915

about

Aromatic sulfonation with sulfur trioxide: mechanism and kinetic model.Noncatalytic bromination of benzene: A combined computational and experimental study.Electrophilic aromatic substitution over zeolites generates Wheland-type reaction intermediates

P2860

Q38815714-8F888513-3FAD-465C-AE70-44E0F890D78F Q52931132-9697B165-E196-4616-9541-5349A86A4EB0 Q57560681-526F8F0C-08BA-4C91-80CC-CF68655E6390

P2860

Arenium ions are not obligatory intermediates in electrophilic aromatic substitution.

http://www.wikidata.org/entity/Q33925915

description

2014 nî lūn-bûn

@nan

2014 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Arenium ions are not obligatory intermediates in electrophilic aromatic substitution.

@ast

Arenium ions are not obligatory intermediates in electrophilic aromatic substitution.

@en

type

label

Arenium ions are not obligatory intermediates in electrophilic aromatic substitution.

@ast

Arenium ions are not obligatory intermediates in electrophilic aromatic substitution.

@en

prefLabel

Arenium ions are not obligatory intermediates in electrophilic aromatic substitution.

@ast

Arenium ions are not obligatory intermediates in electrophilic aromatic substitution.

@en

P1433

Q33925915-718931F8-34EB-4B67-B225-BF3629B706C3

P1476

Q33925915-8F3161AD-B338-4944-A8B7-709CABE5AFDA

P2093

Q33925915-169E1E6E-E27D-45D8-A488-A6979DBFFB9A

Q33925915-2C973F3A-5AA4-48BC-912B-E2C9646B31DE

Q33925915-7EE79EE5-B262-4CDF-99F3-93E93E8800ED

Q33925915-820B34C4-A30F-4660-982C-425949A144AB

Q33925915-843C2C26-B871-415F-9E35-FB7F39205396

Q33925915-F09F3C3A-19A2-4941-A8E5-2A2C3BCDB972

P2860

Q33925915-05811006-04D3-4093-B603-CFA9E84D3F2F

Q33925915-0BFD576F-4B71-4B8B-AD70-CF71285FD89D

Q33925915-0F8BC7AE-E6B1-46A0-945D-F69595408F43

Q33925915-16DB7E11-400F-4DEC-A3AF-CC9995BD4394

Q33925915-223A511F-12DF-457F-872A-2C63588DC6F0

Q33925915-2A543EBF-4342-48E8-91C1-B8E4C53DDBB7

Q33925915-396C2171-3E6B-40BD-A70C-BF6AF6586933

Q33925915-72A9550F-9904-40CD-AB03-54F7E1B0FE6D

Q33925915-7D2FE855-0456-4653-A655-C15C57B435A0

Q33925915-8C6C395D-6269-4D55-8AC9-8FB33F7E1AAE

P304

Q33925915-DCF863C7-3357-4FB0-9C9F-E8C2BB72CF01

P31

Q33925915-47AA8324-65E9-49F8-A46B-35F6E3C230D7

P356

Q33925915-1519D11A-D6ED-4B94-AB1B-D54964886FCF

P407

Q33925915-9C7991D0-1C93-485B-98BD-70A4D3FF0C1C

P433

Q33925915-AD8DEA39-7168-4E5E-8B65-478FC78C3CD9

P478

Q33925915-182340A0-32D2-4905-9F60-1B46357FA3D7

P577

Q33925915-6224E1E3-1AB6-4ECE-A5C3-53E67337AC07

P5875

Q33925915-CCD836F5-E12B-423A-AEF8-72F35AFAB282

P698

Q33925915-7810478B-42EF-4D45-8836-7D2EE9BEE8DB

P932

Q33925915-5116892C-0F10-4B7F-9661-3E34FE579294

P356

PNAS.1405065111

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Arenium ions are not obligatory intermediates in electrophilic aromatic substitution.

@en

P2093

Boriana Hadjieva

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

Boris Galabov

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

Gergana Koleva

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

Henry F Schaefer

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

Paul von Ragué Schleyer

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

Svetlana Simova

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

P2860

Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density

Density-functional thermochemistry. III. The role of exact exchange

Generalized Gradient Approximation Made Simple

Tryptophan 7-halogenase (PrnA) structure suggests a mechanism for regioselective chlorination.

Semiempirical hybrid density functional with perturbative second-order correlation.

Electrophilic aromatic nitration: understanding its mechanism and substituent effects.

A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu.

Electrophile affinity: a reactivity measure for aromatic substitution.

A meta-selective copper-catalyzed C-H bond arylation.

Charge-transfer mechanism for electrophilic aromatic nitration and nitrosation via the convergence of (ab initio) molecular-orbital and Marcus-Hush theories with experiments.

P304

10067-10072

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

P31

scholarly article

P356

10.1073/PNAS.1405065111

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

P407

P433

28

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

P478

111

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

P577

2014-06-27T00:00:00Z

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

P5875

264635982

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

P698

24972792

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

P932

4104905

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