Modification of purine and pyrimidine nucleosides by direct C-H bond activation.

about

Ruthenium-Catalyzed C-H Bond Activation Approach to Azolyl Aminals and Hemiaminal Ethers, Mechanistic Evaluations, and Isomer Interconversion.Synthesis of 8-(1,2,3-triazol-1-yl)-7-deazapurine nucleosides by azide-alkyne click reactions and direct C-H bond functionalization

P2860

Q37194510-AE3C3394-0BE9-41C5-87FA-14894BE8F42B Q41678776-D5F8344B-04B7-4DE5-A51C-0C8CC22FBBA1

P2860

Modification of purine and pyrimidine nucleosides by direct C-H bond activation.

Item

http://www.wikidata.org/entity/Q38383928

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Modification of purine and pyrimidine nucleosides by direct C-H bond activation.

@en

type

Item

label

Modification of purine and pyrimidine nucleosides by direct C-H bond activation.

@en

prefLabel

Modification of purine and pyrimidine nucleosides by direct C-H bond activation.

@en

P1476

Modification of purine and pyrimidine nucleosides by direct C-H bond activation.

@en

P2093

Stanislaw F Wnuk

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

P2860

Formation and stability of a vinyl carbanion at the active site of orotidine 5'-monophosphate decarboxylase: pKa of the C-6 proton of enzyme-bound UMP

(E)-5-(2-Bromovinyl)-2'-deoxyuridine: a potent and selective anti-herpes agent

Inhibitory effects of the guanine moiety on Suzuki couplings of unprotected halonucleosides in aqueous media.

Synthesis of 6,8,9-tri- and 2,6,8,9-tetrasubstituted purines by a combination of the Suzuki cross-coupling, N-arylation, and direct C-H arylation reactions.

C-H bonds as ubiquitous functionality: a general approach to complex arylated imidazoles via regioselective sequential arylation of all three C-H bonds and regioselective N-alkylation enabled by SEM-group transposition.

Direct C-H arylation of purine on solid phase and its use for chemical libraries synthesis.

Catalytic intermolecular direct arylation of perfluorobenzenes.

Palladium-catalyzed benzene arylation: incorporation of catalytic pivalic acid as a proton shuttle and a key element in catalyst design.

Transition-metal-catalyzed direct arylation of (hetero)arenes by C-H bond cleavage.

Palladium-assisted routes to nucleosides.

P304

4874-4901

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

P31

scholarly article

P356

10.3390/MOLECULES20034874

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

Yong Liang

P577

2015-03-17T00:00:00Z

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

P5875

273771708

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

P698

25789821

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

P932

6272170

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

Modification of purine and pyrimidine nucleosides by direct C-H bond activation.

about

P2860

P2860

Modification of purine and pyrimidine nucleosides by direct C-H bond activation.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P932