Suzuki-Miyaura cross-coupling of potassium dioxolanylethyltrifluoroborate and aryl/heteroaryl chlorides.

about

Suzuki-Miyaura cross-coupling of potassium dioxolanylethyltrifluoroborate and aryl/heteroaryl chlorides.

Item

http://www.wikidata.org/entity/Q36874739

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

Suzuki-Miyaura cross-coupling ...... and aryl/heteroaryl chlorides.

@en

type

Item

label

Suzuki-Miyaura cross-coupling ...... and aryl/heteroaryl chlorides.

@en

prefLabel

Suzuki-Miyaura cross-coupling ...... and aryl/heteroaryl chlorides.

@en

P1476

Suzuki-Miyaura cross-coupling ...... and aryl/heteroaryl chlorides.

@en

P2093

Daniel Oehlrich

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

Frederik Rombouts

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

Nicolas Fleury-Brégeot

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

P2860

Organotrifluoroborates: protected boronic acids that expand the versatility of the Suzuki coupling reaction.

Potassium organotrifluoroborates: new perspectives in organic synthesis.

Nickel-catalyzed coupling reactions of alkyl electrophiles, including unactivated tertiary halides, to generate carbon-boron bonds.

Palladium-catalyzed borylation of primary alkyl bromides

Suzuki-Miyaura cross-coupling of potassium alkoxyethyltrifluoroborates: access to aryl/heteroarylethyloxy motifs.

Stereospecific Suzuki cross-coupling of alkyl alpha-cyanohydrin triflates.

Zn-mediated, Pd-catalyzed cross-couplings in water at room temperature without prior formation of organozinc reagents

Highly selective reactions of unbiased alkenyl halides and alkylzinc halides: Negishi-Plus couplings.

Heck alkynylation (copper-free Sonogashira coupling) of aryl and heteroaryl chlorides, using Pd complexes of t-Bu2(p-NMe2C6H4)P: understanding the structure-activity relationships and copper effects.

Diastereoselective synthesis of substituted tetrahydroquinoline-4-carboxylic esters by a tandem reduction-reductive amination reaction.

P304

1536-1539

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

P31

scholarly article

P356

10.1021/OL400320Q

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

Gary A Molander

P577

2013-03-14T00:00:00Z

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

P698

23489071

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

P932

3663905

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