Guanidines: from classical approaches to efficient catalytic syntheses. - Wikidata - wikimedia - TriplyDB

Guanidines: from classical approaches to efficient catalytic syntheses.

Guanidines: from classical approaches to efficient catalytic syntheses.

http://www.wikidata.org/entity/Q38195763

about

Early Main Group Metal Catalysis: How Important is the Metal?Recent development of synthetic preparation methods for guanidines via transition metal catalysis.The chemistry and biology of guanidine natural products.An amidato divalent ytterbium cluster: synthesis and molecular structure, its reactivity to carbodiimides and application in the guanylation reaction.Catalytic addition of amines to carbodiimides by bis(β-diketiminate)lanthanide(II) complexes and mechanistic studies.Tandem Coupling of Azide with Isonitrile and Boronic Acid: Facile Access to Functionalized Amidines.Structural and Mechanistic Insights into s-Block Bimetallic Catalysis: Sodium Magnesiate-Catalyzed Guanylation of Amines.Simple ZnEt2 as a catalyst in carbodiimide hydroalkynylation: structural and mechanistic studies.Synthesis and characterization of bridged bis(amidato) rare earth metal amides and their applications in C-N bond formation reactions.Synthesis and Mechanistic Study of Cyclic Oxoguanidines via Zn(OTf)2 -Catalyzed Guanylation/Amidation from Readily Available Amino Acid Esters and Carbodiimides.Tert -butyl hydroperoxide-promoted guanylation of amines with benzoylthioureas: Mechanistic insights by HRMS and 1 H NMR

P2860

Q29013214-0ABF6F4F-F9F6-435D-843B-91715327F713 Q38258306-BEECA417-5037-4670-A7C2-5B971C9ED8EE Q38675089-B7D7A10D-EE82-4FA7-B24B-402C005E9B2D Q46380264-219E4237-B10A-4308-A1A5-31DB14F866D9 Q46644533-F2467319-5198-400B-B131-5FFF58801547 Q48102948-8E09D618-8F0A-47C7-B623-1242A9395071 Q48270975-F6EEFB81-F425-437A-9579-E87C779F75F7 Q50022315-1D948993-F200-4E93-9CA7-196412586A49 Q51500629-BBBD60DE-664E-497A-B199-574769B73796 Q53491269-F298CE39-D312-4F9D-A148-E3AED704DC1E Q58822266-CC8A8131-8033-4FA0-B04E-0DAE30CB4A69

P2860

Guanidines: from classical approaches to efficient catalytic syntheses.

http://www.wikidata.org/entity/Q38195763

description

article científic

@ca

article scientifique

@fr

articol științific

@ro

articolo scientifico

@it

artigo científico

@gl

artigo científico

@pt

artigo científico

@pt-br

artikel ilmiah

@id

artikull shkencor

@sq

artículo científico

@es

name

Guanidines: from classical approaches to efficient catalytic syntheses.

@en

type

label

Guanidines: from classical approaches to efficient catalytic syntheses.

@en

prefLabel

Guanidines: from classical approaches to efficient catalytic syntheses.

@en

P1433

Q38195763-C7640F17-C3BB-4D18-9AB8-84967F6E1497

P1476

Q38195763-5D101DBA-1432-436C-B516-48CEDD8766FD

P2093

Q38195763-A45D8068-687F-4FFC-B3C2-6CD8797935A5

Q38195763-B3307EED-017B-4A9F-AC1D-A84A42F599DD

Q38195763-D0D20ACE-E3DF-4E49-A4F1-A215C8F4C6CD

Q38195763-EE937595-7AF0-4356-ADEA-04EF3DC403DB

P2860

Q38195763-00B5509E-3F60-4577-AEFC-18A8F0AFED3B

Q38195763-07AF1F48-D4EB-42D5-AB2B-7547043D2A08

Q38195763-0A128D60-7E0C-4460-907F-087F6B2D2E2B

Q38195763-0E959119-16C1-4FB8-8A6E-5CB30A39450D

Q38195763-110F8B4E-565E-45EB-BE11-6B098C40E401

Q38195763-1B03615B-4096-4321-824D-CE5E5EE557C4

Q38195763-2563F058-1180-49A7-A20A-8F05F51048A1

Q38195763-272DD0F1-92F9-444B-B295-76ECEB8DFEAE

Q38195763-32C5DACC-B964-49E5-B982-F5DEFF487371

Q38195763-3F9B475E-88D9-4E8A-A0E9-2BE795C3FF62

P304

Q38195763-F20F42C5-6692-4107-BE37-831B27584E3B

P31

Q38195763-1072FE61-D94F-438C-B42A-454826C8E126

P356

Q38195763-8C159D2A-3D7F-488B-A48C-ADEEFC5BE665

P433

Q38195763-12052990-68D6-496B-8236-20F58C080CA4

P478

Q38195763-66EFD443-CD12-46C8-8B0F-69BB8F5904B7

P50

Q38195763-3B47B540-8965-422C-933B-46BCDBE2AF8C

Q38195763-6812AD7C-95D3-43EE-B9A8-7F966996C35B

Q38195763-7FD452B0-3C81-42D2-B36A-1B00C838B6B1

Q38195763-D36ABAF8-65D5-4374-979F-76D319D82423

P577

Q38195763-1FDCA2F0-F8F3-4B05-865E-E58DF80C8D84

P5875

Q38195763-809E3C8B-9C50-4D47-85B2-62E6651E49B4

P698

Q38195763-E56C20D7-9FCA-4014-932E-3D5854D04204

P356

P1433

Chemical Society Reviews

P1476

Guanidines: from classical approaches to efficient catalytic syntheses

@en

P2093

Antonio Antiñolo

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

Antonio Otero

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

Carlos Alonso-Moreno

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

Fernando Carrillo-Hermosilla

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

P2860

The war against influenza: discovery and development of sialidase inhibitors

Postmetallocene lanthanide-hydrido chemistry: A new family of complexes [{Ln{(Me3Si)2NC(NiPr)2}2(mu-H)}2] (Ln = Y, Nd, Sm, Gd, Yb) supported by guanidinate ligands-synthesis, structure, and catalytic activity in olefin polymerization.

N-hydroxy-N'-aminoguanidines as anti-cancer lead molecule: QSAR, synthesis and biological evaluation.

High DNA affinity of a series of peptide linked diaromatic guanidinium-like derivatives.

Solid-state structure of free base guanidine achieved at last.

The chemistry and biology of organic guanidine derivatives.

Chiral guanidine catalyzed enantioselective reactions.

Synthetic approaches to the neuraminidase inhibitors zanamivir (Relenza) and oseltamivir phosphate (Tamiflu) for the treatment of influenza.

Lanthanide amidinates and guanidinates: from laboratory curiosities to efficient homogeneous catalysts and precursors for rare-earth oxide thin films.

Guanidine chemistry.

P304

3406-3425

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

P31

scholarly article

P356

10.1039/C4CS00013G

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

P433

10

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

P478

43

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

P50

Antonio Antiñolo

Fernando Carrillo-Hermosilla

Carlos Alonso-Moreno

P577

2014-03-14T00:00:00Z

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

P5875

260809917

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

P698

24626874

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