Insertion of arynes into N-halo bonds: a direct approach to o-haloaminoarenes.

about

The role of aryne distortions, steric effects, and charges in regioselectivities of aryne reactions Double heteroatom functionalization of arenes using benzyne three-component coupling.Mild synthesis of triarylsulfonium salts with arynes.

P2860

Q34458865-21185DF5-7065-4774-B52E-3D257C69BEBF Q40214252-2E8213FD-7E3F-42C9-856C-999D4BC6FA0A Q54036624-817B80D3-E404-4969-ABFB-37749B6CC137

P2860

Insertion of arynes into N-halo bonds: a direct approach to o-haloaminoarenes.

Item

http://www.wikidata.org/entity/Q38797381

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

2013年论文

@zh

2013年论文

@zh-cn

name

Insertion of arynes into N-halo bonds: a direct approach to o-haloaminoarenes.

@en

type

Item

label

Insertion of arynes into N-halo bonds: a direct approach to o-haloaminoarenes.

@en

prefLabel

Insertion of arynes into N-halo bonds: a direct approach to o-haloaminoarenes.

@en

P1476

Insertion of arynes into N-halo bonds: a direct approach to o-haloaminoarenes.

@en

P2093

Charles E Hendrick

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

Qiu Wang

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

Stacey L McDonald

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

P2860

Design and evaluation of 3,6-di(hetero)aryl imidazo[1,2-a]pyrazines as inhibitors of checkpoint and other kinases

Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides

Indolyne and aryne distortions and nucleophilic regioselectivites

Selective antagonists of mouse trace amine-associated receptor 1 (mTAAR1): discovery of EPPTB (RO5212773).

Cariprazine (RGH-188), a dopamine D(3) receptor-preferring, D(3)/D(2) dopamine receptor antagonist-partial agonist antipsychotic candidate: in vitro and neurochemical profile.

Experimental and theoretical investigations into the unusual regioselectivity of 4,5-, 5,6-, and 6,7-indole aryne cycloadditions

One century of aryne chemistry.

Arynes and cyclohexyne in natural product synthesis.

Palladium-catalyzed coupling reactions of aryl chlorides.

Structure-functional selectivity relationship studies of β-arrestin-biased dopamine D₂ receptor agonists.

P304

3444-3447

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

P31

scholarly article

P356

10.1021/OL401518C

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

P577

2013-06-24T00:00:00Z

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

P698

23796022

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

P932

4779594

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

Insertion of arynes into N-halo bonds: a direct approach to o-haloaminoarenes.

about

P2860

P2860

Insertion of arynes into N-halo bonds: a direct approach to o-haloaminoarenes.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932