Visible-light induced di- and trifluoromethylation of N-benzamides with fluorinated sulfones for the synthesis of CF2H/CF3-containing isoquinolinediones.

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Visible-light induced di- and trifluoromethylation of N-benzamides with fluorinated sulfones for the synthesis of CF2H/CF3-containing isoquinolinediones.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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name

Visible-light induced di- and ...... containing isoquinolinediones.

@en

Visible-light induced di- and ...... containing isoquinolinediones.

@nl

type

Item

label

Visible-light induced di- and ...... containing isoquinolinediones.

@en

Visible-light induced di- and ...... containing isoquinolinediones.

@nl

prefLabel

Visible-light induced di- and ...... containing isoquinolinediones.

@en

Visible-light induced di- and ...... containing isoquinolinediones.

@nl

P1476

Visible-light induced di- and ...... containing isoquinolinediones.

@en

P2093

Guanglong Zou

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

Xuelin Wang

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P2860

A new reagent for direct difluoromethylation

Use of fluoroform as a source of difluorocarbene in the synthesis of difluoromethoxy- and difluorothiomethoxyarenes.

4-Substituted 2-Hydroxyisoquinoline-1,3(2H,4H)-diones as a Novel Class of HIV-1 Integrase Inhibitors

Synopsis of some recent tactical application of bioisosteres in drug design.

Design, synthesis, biochemical, and antiviral evaluations of C6 benzyl and C6 biarylmethyl substituted 2-hydroxylisoquinoline-1,3-diones: dual inhibition against HIV reverse transcriptase-associated RNase H and polymerase with antiviral activities.

Cascade couplings of N-alkyl-N-methacryloyl benzamides with ethers and benzenesulfonohydrazides to generate isoquinoline-1,3(2H,4H)-dione derivatives.

Cascade alkylarylation of substituted N-allylbenzamides for the construction of dihydroisoquinolin-1(2H)-ones and isoquinoline-1,3(2H,4H)-diones

Introduction of fluorine and fluorine-containing functional groups.

Magnesium chelating 2-hydroxyisoquinoline-1,3(2H,4H)-diones, as inhibitors of HIV-1 integrase and/or the HIV-1 reverse transcriptase ribonuclease H domain: discovery of a novel selective inhibitor of the ribonuclease H function.

Discovery of 4-(benzylaminomethylene)isoquinoline-1,3-(2H,4H)-diones and 4-[(pyridylmethyl)aminomethylene]isoquinoline-1,3-(2H,4H)-diones as potent and selective inhibitors of the cyclin-dependent kinase 4.

P304

8748-8754

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P31

scholarly article

P356

10.1039/C7OB02226C

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P433

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

P478

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

P577

2017-10-09T00:00:00Z

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P698

28991964

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