Nickel-catalyzed ring-opening of α-hydroxycyclobutenones with a remarkable ligand effect.

about

Nickel-catalyzed ring-opening of α-hydroxycyclobutenones with a remarkable ligand effect.

Item

http://www.wikidata.org/entity/Q50169916

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

Nickel-catalyzed ring-opening of α-hydroxycyclobutenones with a remarkable ligand effect.

@en

Nickel-catalyzed ring-opening of α-hydroxycyclobutenones with a remarkable ligand effect.

@nl

type

Item

label

Nickel-catalyzed ring-opening of α-hydroxycyclobutenones with a remarkable ligand effect.

@en

Nickel-catalyzed ring-opening of α-hydroxycyclobutenones with a remarkable ligand effect.

@nl

prefLabel

Nickel-catalyzed ring-opening of α-hydroxycyclobutenones with a remarkable ligand effect.

@en

Nickel-catalyzed ring-opening of α-hydroxycyclobutenones with a remarkable ligand effect.

@nl

P1476

Nickel-catalyzed ring-opening of α-hydroxycyclobutenones with a remarkable ligand effect

@en

P2093

Songsong Gao

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

P2860

Carbon-carbon bond activation of cyclobutenones enabled by the addition of chiral organocatalyst to ketone

3-Acylated tetramic and tetronic acids as natural metal binders: myth or reality?

Tetramic and tetronic acids: an update on new derivatives and biological aspects.

Thermodynamic control of the electrocyclic ring opening of cyclobutenes: C=X substituents at C-3 mask the kinetic torquoselectivity.

Total synthesis of cribrostatin 6.

Cyclobutenones and Benzocyclobutenones: Versatile Synthons in Organic Synthesis.

Cyclobutenone as a highly reactive dienophile: expanding upon Diels-Alder paradigms.

Computational Study of Rh-Catalyzed Carboacylation of Olefins: Ligand-Promoted Rhodacycle Isomerization Enables Regioselective C-C Bond Functionalization of Benzocyclobutenones.

Highly efficient synthesis of 3-amino-/alkylthio-cyclobut-2-en-1-ones based on the cyclization of acyl ketene dithioacetals.

Substituent effect of group 14 elements on the ring-opening reaction of cyclobutene.

P304

10540-10543

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

P31

scholarly article

P356

10.1039/C7CC03340K

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

Xiangdong Hu

P577

2017-09-01T00:00:00Z

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

P698

28890958

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

P921

Iztāctepoztli