Synthesis of pyrazolopyrimidinones using a “one-pot” approach under microwave irradiation.

about

Synthesis of pyrazolopyrimidinones using a “one-pot” approach under microwave irradiation.

Item

http://www.wikidata.org/entity/Q55444200

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh

2018年學術文章

@zh-hant

name

Synthesis of pyrazolopyrimidin ...... h under microwave irradiation.

@en

Synthesis of pyrazolopyrimidin ...... h under microwave irradiation.

@nl

type

Item

label

Synthesis of pyrazolopyrimidin ...... h under microwave irradiation.

@en

Synthesis of pyrazolopyrimidin ...... h under microwave irradiation.

@nl

prefLabel

Synthesis of pyrazolopyrimidin ...... h under microwave irradiation.

@en

Synthesis of pyrazolopyrimidin ...... h under microwave irradiation.

@nl

P1476

Synthesis of pyrazolopyrimidinones using a "one-pot" approach under microwave irradiation

@en

P2093

John C Stephens

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

John M D Walsh

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

Patrick McArdle

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

Robert W Devine

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

P2860

Identification of potent, selective KDM5 inhibitors

The identification a novel, selective, non-steroidal, functional glucocorticoid receptor antagonist.

Aminopyrazolo[1,5-a]pyrimidines as potential inhibitors of Mycobacterium tuberculosis: Structure activity relationships and ADME characterization.

Evaluation of 7-arylaminopyrazolo[1,5-a]pyrimidines as anti-Plasmodium falciparum, antimalarial, and Pf-dihydroorotate dehydrogenase inhibitors.

Synthesis of pyrazolo[3,4-b]pyridines under microwave irradiation in multi-component reactions and their antitumor and antimicrobial activities - Part 1.

Microwave-assisted synthesis of N-pyrazole ureas and the p38alpha inhibitor BIRB 796 for study into accelerated cell ageing.

Synthesis and antiproliferative activity in vitro of new 2-, 3- or 4-substituted pyrido[2',3':3,4]pyrazolo[1, 5-a]pyrimidines.

Discovery and characterization of a novel 7-aminopyrazolo[1,5-a]pyrimidine analog as a potent hepatitis C virus inhibitor.

IND-2, a pyrimido[1″,2″:1,5]pyrazolo[3,4-b]quinoline derivative, circumvents multi-drug resistance and causes apoptosis in colon cancer cells.

Synthesis and SAR of azolopyrimidines as potent and selective dipeptidyl peptidase-4 (DPP4) inhibitors for type 2 diabetes.

P304

1222-1228

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

P31

scholarly article

P356

10.3762/BJOC.14.104

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

P478

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

P50

Mark Kelada

P577

2018-05-28T00:00:00Z

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

P698

29977390

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

P932

6009099

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