Synthesis of 2-Indolyltetrahydroquinolines by Zinc(II)-Catalyzed Intramolecular Hydroarylation-Redox Cross-Dehydrogenative Coupling of N -Propargylanilines with Indoles

about

Synthesis of 2-Indolyltetrahydroquinolines by Zinc(II)-Catalyzed Intramolecular Hydroarylation-Redox Cross-Dehydrogenative Coupling of N -Propargylanilines with Indoles

Item

http://www.wikidata.org/entity/Q58615087

description

scientific article published on 21 April 2016

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована у квітні 2016

@uk

name

Synthesis of 2-Indolyltetrahydroquinolines by Zinc

@nl

Synthesis of 2-Indolyltetrahyd ...... Propargylanilines with Indoles

@en

type

Item

label

Synthesis of 2-Indolyltetrahydroquinolines by Zinc

@nl

Synthesis of 2-Indolyltetrahyd ...... Propargylanilines with Indoles

@en

prefLabel

Synthesis of 2-Indolyltetrahydroquinolines by Zinc

@nl

Synthesis of 2-Indolyltetrahyd ...... Propargylanilines with Indoles

@en

P1476

Synthesis of 2-Indolyltetrahyd ...... Propargylanilines with Indoles

@en

P2093

Guangzhe Li

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

P2860

Chemistry and biology of the tetrahydroisoquinoline antitumor antibiotics.

Cu-catalyzed cross-dehydrogenative coupling: a versatile strategy for C-C bond formations via the oxidative activation of sp(3) C-H bonds.

Ruthenium catalyzed biomimetic oxidation in organic synthesis inspired by cytochrome P-450.

Advances in the chemistry of tetrahydroquinolines.

The cross-dehydrogenative coupling of C(sp3)-H bonds: a versatile strategy for C-C bond formations.

Ecteinascidins. A review of the chemistry, biology and clinical utility of potent tetrahydroisoquinoline antitumor antibiotics.

Direct functionalization of (un)protected tetrahydroisoquinoline and isochroman under iron and copper catalysis: two metals, two mechanisms.

Facile, solvent and ligand free iron catalyzed direct functionalization of N-protected tetrahydroisoquinolines and isochroman.

Rhodium-catalyzed intramolecular hydroarylation of 1-halo-1-alkynes: regioselective synthesis of semihydrogenated aromatic heterocycles.

Gold-catalyzed intramolecular allylic amination of 2-tosylaminophenylprop-1-en-3-ols. A concise synthesis of (+/-)-angustureine.

P304

6758-6761

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

P31

scholarly article

P356

10.1002/ANIE.201602416

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

Hiroyuki Nakamura

Guangzhe Li

P577

2016-04-21T00:00:00Z

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

P698

27097846

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

P921

catalysis

general chemistry